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2,341 results on '"Medical test kit industry -- Product defects and recalls"'

1. Baxter Initiates Heparin Recall Over Elevated Endotoxin Levels

Author

Ernst, Diana

Subjects
Baxter International Inc. (Deerfield, Illinois) -- Product defects and recalls, Heparin -- Contamination -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Health
Abstract

Baxter International is recalling 1 lot of Heparin Sodium in 0.9% Sodium Chloride Injection due to the potential for elevated endotoxin levels. The recall was initiated after lot number N008235 [...]

Published
2024

2. Reports of Injuries, Deaths Prompt FDA to Recall Heart Failure Devices

Subjects
United States. Food and Drug Administration, Thoratec Corp. -- Product defects and recalls, Abbott Laboratories (Abbott Park, Illinois) -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Product recalls, Medical equipment and supplies industry -- Product defects and recalls, Heart, Pharmaceutical industry -- Product defects and recalls, Product recall, Health
Abstract

HealthDay News — The HeartMate II and HeartMate 3, manufactured by Thoratec Corp., a subsidiary of Abbott Laboratories, are now under a strict US Food and Drug Administration recall after [...]

Published
2024

3. Reports of Injuries, Deaths Prompt FDA to Recall Heart Failure Devices

Subjects
United States. Food and Drug Administration, Thoratec Corp. -- Product defects and recalls, Abbott Laboratories (Abbott Park, Illinois) -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Product recalls, Medical equipment and supplies industry -- Product defects and recalls, Heart, Pharmaceutical industry -- Product defects and recalls, Product recall, Health
Abstract

HealthDay News — The HeartMate II and HeartMate 3, manufactured by Thoratec Corp., a subsidiary of Abbott Laboratories, are now under a strict US Food and Drug Administration recall after [...]

Published
2024

4. Boston Scientific recalls 1,594 Obsidio Embolic devices in U.S

Subjects
Boston Scientific Corp. -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Product recalls, Medical equipment and supplies industry -- Product defects and recalls, Product recall, Business, News, opinion and commentary
Abstract

Boston Scientific Corporation is recalling 1,594 Obsidio Embolic devices in the U.S. by issuing a correction, according to a post from the FDA. An investigation determined that delivery of Obsidio [...]

Published
2024

5. DYNAREX CORPORATION RECALLS PRODUCT DUE TO POSSIBLE HEALTH RISK

Subjects
United States. Food and Drug Administration, Dynarex Corp. -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Product recalls -- Health aspects, Medical equipment and supplies industry -- Product defects and recalls, Product recall, News, opinion and commentary
Abstract

MONTVALE, N.J. -- The following information was released by the U.S. Food and Drug Administration (FDA): Dynarex Corporation is recalling 62 cases of item number 4875, Dynacare Baby Powder, Batch [...]

Published
2024

6. BAXTER ISSUES VOLUNTARY NATIONWIDE RECALL OF ONE LOT OF HEPARIN SODIUM 0.9% SODIUM CHLORIDE INJECTION DUE TO POTENTIAL FOR ELEVATED ENDOTOXIN LEVELS

Subjects
United States. Food and Drug Administration, Baxter International Inc. (Deerfield, Illinois) -- Product defects and recalls, Heparin -- Contamination -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, News, opinion and commentary
Abstract

DEERFIELD, Ill -- The following information was released by the U.S. Food and Drug Administration (FDA): Baxter International Inc. (NYSE:BAX) is voluntarily recalling one lot of Heparin Sodium in 0.9% [...]

Published
2024

7. BAXTER ISSUES URGENT MEDICAL DEVICE RECALL FOR VOLARA SYSTEM SINGLE-PATIENT USE CIRCUIT

Subjects
United States. Food and Drug Administration, Baxter International Inc. (Deerfield, Illinois) -- Product defects and recalls, Medical equipment -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Product recalls, Medical equipment and supplies industry -- Product defects and recalls, Physiological apparatus -- Product defects and recalls, Product recall, News, opinion and commentary
Abstract

DEERFIELD, Ill. -- The following information was released by the U.S. Food and Drug Administration (FDA): Summary Company Announcement Date: July 15, 2024 FDA Publish Date: July 16, 2024 Product [...]

Published
2024

8. FDA Recalls Heart Failure Devices Linked to Injuries and Deaths

Subjects
United States. Food and Drug Administration, Thoratec Corp. -- Product defects and recalls, Abbott Laboratories (Abbott Park, Illinois) -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Product recalls, Medical equipment and supplies industry -- Product defects and recalls, Cardiac patients, Pharmaceutical industry -- Product defects and recalls, Product recall, Health
Abstract

Byline: Ernie Mundell HealthDay Reporter WEDNESDAY, April 17, 2024 (HealthDay News) -- Two implanted heart devices used by patients in end-stage heart failure are now under a strict U.S. Food [...]

Published
2024

9. FDA Announces Recall of Heart Pumps Linked to Deaths and Injuries

Author

Parmar, Arundhati

Subjects
Thoratec Corp. -- Product defects and recalls, Abbott Laboratories (Abbott Park, Illinois) -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Pharmaceutical industry -- Product defects and recalls
Abstract

https://medcitynews.com/2024/04/fda-announces-recall-of-heart-pumps-linked-to-deaths-and-injuries/ The recall comes years after surgeons say they first noticed problems with the HeartMate II and HeartMate 3, manufactured by Thoratec Corp., a subsidiary of Abbott Laboratories. The devices [...]

Published
2024

10. MEDTRONIC NAVIGATION INC. RECALLS STEALTHSTATION S8 APPLICATION VERSION 2.0 AND 2.0.1 DUE TO A SOFTWARE GLITCH

Subjects
United States. Food and Drug Administration, Medtronic Navigation Inc. -- Product defects and recalls, Program errors -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, News, opinion and commentary
Abstract

SILVER SPRING, MD -- The following information was released by the U.S. Food and Drug Administration (FDA): Recalled Product Product Names: StealthStation S8 Application Version 2.0 and 2.0.1 Product Codes: [...]

Published
2023

11. J&J's Abiomed Comments on Most Recent Impella Recall

Subjects
United States. Food and Drug Administration, Abiomed Inc. -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Health care industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Health care industry, Science and technology
Abstract

Abiomed's June 29 recall of Impella RP Flex with SmartAssist system catheters for blood clot risk has been identified as Class I by the U.S. Food and Drug Administration (FDA). [...]

Published
2023

12. Becton Dickinson announces voluntary recall of intraosseous products

Subjects
Becton, Dickinson and Co. -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Product recalls, Medical equipment and supplies industry -- Product defects and recalls, Product recall, Business, News, opinion and commentary
Abstract

Becton Dickinson announced a voluntary recall on the BD Intraosseous Needle Set Kits, BD Intraosseous Manual Driver Kits and BD Intraosseous Powered Drivers. Certain lots within the expiration date of [...]

Published
2022

13. Teleflex Incorporated Announces Global Recall of Rusch Endotracheal Tubes

Subjects
Teleflex Inc. -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Banking, finance and accounting industries, Business
Abstract

WAYNE, Pa., June 21, 2023 (GLOBE NEWSWIRE) -- Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies for critical care and surgery, has announced a global recall of [...]

Published
2023

14. ABIOMED RECALLS SPECIFIC IMPELLA 5.5 WITH SMARTASSIST FOR PURGE FLUID LEAKS THAT CAN CAUSE PUMP STOP AND LOSS OF SUPPORT

Subjects
United States. Food and Drug Administration, Abiomed Inc. -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Heart, News, opinion and commentary
Abstract

SILVER SPRING, MD -- The following information was released by the U.S. Food and Drug Administration (FDA): Device Use The Impella 5.5 with SmartAssist System is used for up to [...]

Published
2023

15. FDA posts Class 1 device recall for Boston Scientific's VICI venous stent

Subjects
Boston Scientific Corp. -- Product defects and recalls, Stent (Surgery) -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Product recalls, Medical equipment and supplies industry -- Product defects and recalls, Product recall, Business, News, opinion and commentary
Abstract

The FDA posted a notice, dated May 19, that indicates that Boston Scientific initiated a Class 1 device recall of its VICI venous stent as of April 12, 2021. [Reference [...]

Published
2021

16. Correction: FDA posts recall for Boston Scientific's VICI venous stent

Subjects
Becton, Dickinson and Co. -- Product defects and recalls, Boston Scientific Corp. -- Product defects and recalls, Stent (Surgery) -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Business, News, opinion and commentary
Abstract

This corrects a prior report that incorrectly attributed the recall to Becton Dickinson [...]

Published
2021

17. FDA posts Class 1 device recall for Becton Dickinson's VICI venous stent

Subjects
Becton, Dickinson and Co. -- Product defects and recalls, Stent (Surgery) -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Product recalls, Medical equipment and supplies industry -- Product defects and recalls, Product recall, Business, News, opinion and commentary
Abstract

The FDA posted a notice, dated May 19, that indicates that Becton Dickinson initiated a Class 1 device recall of its VICI venous stent as of April 12, 2021. [Reference [...]

Published
2021

18. Baxter recalls WatchCare Incontinence Management System, due to risk of interference

Subjects
Baxter International Inc. (Deerfield, Illinois) -- Product defects and recalls, Medical equipment -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Physiological apparatus -- Product defects and recalls, Urinary incontinence, General interest, News, opinion and commentary
Abstract

The FDA classified Baxter International Inc's BAX recall of hospital bed systems as the most serious type of concern that could lead to life-threatening injury or death. Baxter has initiated [...]

Published
2022

19. Becton Dickinson voluntarily recalling specified lots of ChloraPrep applicator

Subjects
Becton, Dickinson and Co. -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Business, News, opinion and commentary
Abstract

Becton, Dickinson and Company announced that it is voluntarily recalling specified lots of the ChloraPrep Hi-Lite Orange 26 mL Applicator to the user level due to a defective applicator. The [...]

Published
2021

20. HeartWare HVAD System Batteries Are Recalled By Medtronic Due To Electrical Issues

Subjects
Medtronic PLC -- Product defects and recalls, Batteries -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Cardiac patients, Heart -- Transplantation, Business, international
Abstract

MEDTRONIC PLC (NYSE:MDT) is recalling HeartWare HVAD System batteries because they may experience electrical faults that cause the system to fail unexpectedly. The HeartWare Ventricular Assist Device (HVAD) System is [...]

Published
2022

21. Home Antigen Test Recall Affects Millions: Beware False Positives, but Also Uncertainty and Potential False Negatives

Author

Kost, Gerald J.

Subjects
United States. Food and Drug Administration -- Laws, regulations and rules, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Diagnostic errors -- Risk factors, Government regulation, Health
Abstract

To the Editor.--On November 10, 2021, the US Food and Drug Administration (FDA) announced a class I recall, 'Potential for false positive results with certain lots of Ellume coronavirus disease-19 [...]

Published
2022
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22. BD Announces Voluntary Recall on Intraosseous Products

Subjects
Becton, Dickinson and Co. -- Product defects and recalls, High technology industry, Medical test kit industry -- Product defects and recalls, Product recalls, Medical equipment and supplies industry -- Product defects and recalls, Product recall, General interest, News, opinion and commentary
Abstract

FRANKLIN LAKES: BD (Becton, Dickinson and Company) has issued the following news release: BD (Becton, Dickinson and Company), a leading global medical technology company, announced a voluntary recall on the [...]

Published
2022

23. Philips issues voluntary recall for CPAP machines, ventilators

Author

Varine, Patrick

Subjects
Medical equipment -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Physiological apparatus -- Product defects and recalls, General interest, News, opinion and commentary
Abstract

Byline: Patrick Varine Jun. 15Medical equipment company Philips has issued a recall on some products to address possible health risks associated with a foam component meant to help reduce noise. [...]

Published
2021

24. WIRION(r) Embolic Protection System is being voluntarily recalled by Cardiovascular Systems, Inc

Subjects
Cardiovascular Systems Inc. -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, General interest, News, opinion and commentary
Abstract

ST. PAUL, Minn.: Cardiovascular Systems, Inc. has initiated a voluntary recall of unused WIRION Embolic Protection Systems (WIRION) due to complaints of filter breakage during retrieval. CSI is voluntarily recalling [...]

Published
2021

25. Cardiovascular Systems, Inc. Initiates Voluntary Recall of WIRION[R] Embolic Protection System

Subjects
United States. Food and Drug Administration -- Planning, Cardiovascular Systems Inc. -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Company business planning, Business, Business, international
Abstract

ST. PAUL, Minn. -- Cardiovascular Systems, Inc. (CSI([R])) (NASDAQ: CSII) has initiated a voluntary recall of unused WIRION Embolic Protection Systems (WIRION) due to complaints of filter breakage during retrieval. [...]

Published
2021

26. News Flash:LUCIRA HEALTH Provides Statement on Copan's Recall of its FLOQSwabs

Subjects
Lucira Health Inc. -- Product defects and recalls, High technology industry, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, General interest, News, opinion and commentary
Abstract

Lucira Health, Inc. ('Lucira Health' or 'Lucira') (NASDAQ: LHDX), a medical technology company focused on the development and commercialization of transformative and innovative infectious disease test kits, today commented on [...]

Published
2021

27. LUCIRA(TM) HEALTH Provides Statement on Copan's Recall of its FLOQSwabs

Subjects
Lucira Health Inc. -- Product defects and recalls, High technology industry, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Banking, finance and accounting industries, Business
Abstract

EMERYVILLE, Calif., Oct 08, 2021 (GLOBE NEWSWIRE via COMTEX) -- Lucira Health, Inc. ('Lucira Health' or 'Lucira') (NASDAQ: LHDX), a medical technology company focused on the development and commercialization of [...]

Published
2021

28. Medtronic Expands Recall to Include More Than 463,000 Insulin Pumps

Subjects
Medtronic PLC -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Insulin pumps -- Product defects and recalls, Health
Abstract

TUESDAY, Oct. 5, 2021 (HealthDay News) -- Medtronic has expanded a recall of its MiniMed 600 series insulin pumps to include more than 463,000 of the devices. The pumps may [...]

Published
2021

29. Sleep Apnea Patients Struggle as Common CPAP Machine Is Recalled

Author

Thompson, Dennis

Subjects
Respironics Inc. -- Product defects and recalls, Continuous positive airway pressure -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Sleep apnea syndromes -- Care and treatment, Ventilators -- Product defects and recalls, Health
Abstract

Byline: Dennis Thompson HealthDay Reporter MONDAY, Sept. 20, 2021 (HealthDay News) -- Millions of U.S. sleep apnea patients are scrambling to find ways to protect their nightly slumber, following a [...]

Published
2021

30. ICU MEDICAL ISSUES A VOLUNTARY NATIONWIDE RECALL OF AMINOSYN II 15%, AN AMINO ACID INJECTION, SULFITE FREE IV SOLUTION DUE TO THE PRESENCE OF PARTICULATE MATTER

Subjects
United States. Food and Drug Administration, ICU Medical Inc. -- Product defects and recalls, Sulfites -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Amino acids -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, News, opinion and commentary
Abstract

SILVER SPRING, MD -- The following information was released by the U.S. Food and Drug Administration (FDA): ICU Medical, Inc. is voluntarily recalling one lot (2,112 units) of Aminosyn II, [...]

Published
2021

31. ICU Medical Issues a Voluntary Nationwide Recall of Aminosyn II 15%, An Amino Acid Injection, Sulfite Free IV Solution Due to the Presence of Particulate Matter

Subjects
ICU Medical Inc. -- Product defects and recalls, Sulfites -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Amino acids -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, General interest, News, opinion and commentary
Abstract

LAKE FOREST: ICU Medical, Inc. has issued the following news release: ICU Medical, Inc. is voluntarily recalling one lot (2,112 units) of Aminosyn II, 15%, An Amino Acid Injection, Sulfite [...]

Published
2021

32. Bernstein Liebhard LLP Investigating Injuries and Illness Allegedly Caused by Recalled Philips CPAP Machines, BiPAP Machines, and Mechanical Ventilators

Subjects
Respironics Inc. -- Product defects and recalls, Medical research -- Investigations, Medicine, Experimental -- Investigations, Lung diseases -- Investigations, Law firms -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Machinery -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Ventilators -- Product defects and recalls, Magneto-electric machines -- Product defects and recalls, Company legal issue, General interest, News, opinion and commentary
Abstract

NEW YORK: Bernstein Liebhard LLP has issued the following news release: Bernstein Liebhard LLP, a nationwide law firm representing the victims of defective drugs and medical devices, is investigating serious [...]

Published
2021

33. Bernstein Liebhard LLP Investigating Injuries and Illness Allegedly Caused by Recalled Philips CPAP Machines, BiPAP Machines, and Mechanical Ventilators

Subjects
Respironics Inc. -- Product defects and recalls, Medical research -- Investigations, Medicine, Experimental -- Investigations, Lung diseases -- Investigations, Law firms -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Machinery -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Ventilators -- Product defects and recalls, Magneto-electric machines -- Product defects and recalls, Company legal issue, Business, News, opinion and commentary
Abstract

Polyester-Based Polyurethane Foam Used in Philips Respironics' Assisted Breathing Devices May Degrade, Placing Patients at Risk for Serious Lung Injuries and Cancer. NEW YORK, Aug. 20, 2021 /PRNewswire/ -- Bernstein [...]

Published
2021

34. Boston Scientific Recalls 48,000 Pacemakers

Subjects
Boston Scientific Corp. -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Pacemaker, Artificial (Heart) -- Product defects and recalls, Business, international, Law
Abstract

A recent Cardiovascular Business article discussed the FDA recall of 48,000 heart devices manufactured by Boston Scientific. The reason for the recall is the potential for an incorrect transition into [...]

Published
2021

35. RECON: MODERNA TO MANUFACTURE MRNA VACCINES IN CANADA; BOSTON SCIENTIFIC RECALLS 48,000 INGENIO PACEMAKERS

Subjects
Merck & Company Inc. -- Product defects and recalls, CNBC L.L.C. -- Product defects and recalls, Pfizer Inc. -- Product defects and recalls, Colgate-Palmolive Co. -- Product defects and recalls, Boston Scientific Corp. -- Product defects and recalls, Medical research, Drug approval, Pacemaker, Artificial (Heart) -- Product defects and recalls, Organ transplant recipients, Pharmaceutical industry -- Product defects and recalls, Cable television broadcasting industry -- Product defects and recalls, Medicine, Experimental, Vaccination, Medical test kit industry -- Product defects and recalls, Toiletries industry -- Product defects and recalls, Ophthalmic drugs -- Contamination -- Product defects and recalls, Messenger RNA, Medical equipment and supplies industry -- Product defects and recalls, Vaccines -- Contamination -- Product defects and recalls, News, opinion and commentary
Abstract

ROCKVILLE, MD -- The following information was released by the Regulatory Affairs Professionals Society: By Michael Mezher Welcome to Regulatory Reconnaissance, your daily regulatory news and intelligence briefing. In Focus: [...]

Published
2021

36. Health Highlights: June 3, 2021

Author

Preidt, Robert

Subjects
United States. Food and Drug Administration -- Powers and duties, United States. Centers for Disease Control and Prevention -- Powers and duties, Medtronic PLC -- Product defects and recalls, SCYNEXIS Chemistry and Automation Inc. -- Product introduction, Dementia -- Forecasts and trends, Frozen chicken -- Health aspects, Cardiovascular instruments, Implanted -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Racism, Football players -- Health aspects, Medical equipment and supplies industry -- Product defects and recalls, Antifungal agents -- Prices and rates -- Product introduction, Candidiasis, Vulvovaginal -- Drug therapy, Salmonella -- Health aspects, Pharmaceutical industry -- Product introduction, Market trend/market analysis, Company pricing policy, Health, National Football League -- Powers and duties
Abstract

Byline: Robert Preidt HealthDay Reporter NFL Scraps Race-Based Evaluations of Dementia Claims by Former Players A controversial race-based method of evaluating dementia claims by former NFL players will be scrapped, [...]

Published
2021

37. MEDICAL ACTION INDUSTRIES RECALLS KITS DUE TO CONTAMINATION RISK

Subjects
United States. Food and Drug Administration, Medical Action Industries Inc. -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Product recalls, Medical equipment and supplies industry -- Product defects and recalls, Product recall, News, opinion and commentary
Abstract

WASHINGTON, DC -- The following information was released by the American Hospital Association (AHA): Medical Action Industries Inc. has recalled more than 8,000 medical convenience kits due to fungal contamination [...]

Published
2021

38. BD Announces the Voluntary Recall of Specified Lots of ChloraPrep Hi-Lite Orange 26 mL Applicator in the United States and U.S. Territories Due to Defective Applicator

Subjects
United States. Food and Drug Administration, Becton, Dickinson and Co. -- Product defects and recalls, High technology industry, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, General interest, News, opinion and commentary
Abstract

FRANKLIN LAKES: BD (Becton, Dickinson and Company) has issued the following news release: BD (Becton, Dickinson and Company), a leading global medical technology company, is voluntarily recalling specified lots of [...]

Published
2021

39. BD Announces the Voluntary Recall of Specified Lots of ChloraPrep(TM) Hi-Lite Orange(TM) 26 mL Applicator in the United States and U.S. Territories Due to Defective Applicator

Subjects
Becton, Dickinson and Co. -- Product defects and recalls, High technology industry, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Business, News, opinion and commentary
Abstract

FRANKLIN LAKES, N.J., April 20, 2021 /PRNewswire/ -- BD (Becton, Dickinson and Company), a leading global medical technology company, is voluntarily recalling specified lots of the ChloraPrep[sup.(TM) ]Hi-Lite Orange(TM) 26 [...]

Published
2021

40. BD ANNOUNCES THE VOLUNTARY RECALL OF SPECIFIED LOTS OF CHLORAPREPA'cents HI-LITE ORANGEA'cents 26 ML APPLICATOR IN THE UNITED STATES AND U.S. TERRITORIES DUE TO DEFECTIVE APPLICATOR

Subjects
United States. Food and Drug Administration, Becton, Dickinson and Co. -- Product defects and recalls, High technology industry -- Health aspects, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, News, opinion and commentary
Abstract

SILVER SPRING, MD -- The following information was released by the U.S. Food and Drug Administration (FDA): BD (Becton, Dickinson and Company), a leading global medical technology company, is voluntarily [...]

Published
2021

41. BD EXPANDS VOLUNTARY RECALL OF CHLORAPREPA'cents 3 ML APPLICATOR NATIONWIDE TO INCLUDE ALL U.S. STATES

Subjects
United States. Food and Drug Administration, Becton, Dickinson and Co. -- Product defects and recalls, High technology industry, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, News, opinion and commentary
Abstract

SILVER SPRING, MD -- The following information was released by the U.S. Food and Drug Administration (FDA): BD (Becton, Dickinson and Company), a leading global medical technology company, has revised [...]

Published
2021

42. MEDTRONIC ANNOUNCES VOLUNTARY RECALL OF UNUSED VALIANT NAVIONA'cents THORACIC STENT GRAFT SYSTEM

Subjects
United States. Food and Drug Administration, Medtronic PLC -- Product defects and recalls, Patients -- Care and treatment, Stent (Surgery) -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, News, opinion and commentary
Abstract

SILVER SPRING, MD -- The following information was released by the U.S. Food and Drug Administration (FDA): Company Announcement Medtronic plc (NYSE:MDT), the global leader in medical technology, has voluntarily [...]

Published
2021

43. Medtronic Announces Voluntary Recall of Unused Valiant Navion(TM) Thoracic Stent Graft System

Subjects
Medtronic PLC -- Product defects and recalls, Patients -- Care and treatment, Stent (Surgery) -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Business, News, opinion and commentary
Abstract

DUBLIN, Feb. 17, 2021 /PRNewswire/ -- Medtronic plc (NYSE:MDT), the global leader in medical technology, has voluntarily issued a global recall of unused Medtronic Valiant Navion(TM) thoracic stent graft system [...]

Published
2021

44. ICU Medical Issues a Voluntary Nationwide Recall of Aminosyn II 15%, An Amino Acid Injection, Sulfite Free IV Solution Due to the Presence of Particulate Matter

Subjects
ICU Medical Inc. -- Product defects and recalls, Sulfites -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Amino acids -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Chemistry
Abstract

M2 PHARMA-September 3, 2021-ICU Medical Issues a Voluntary Nationwide Recall of Aminosyn II 15%, An Amino Acid Injection, Sulfite Free IV Solution Due to the Presence of Particulate Matter (C)2021 [...]

Published
2021

45. Shedding suppliers

Author

Barbella, Michael

Subjects
United States. Food and Drug Administration -- Laws, regulations and rules -- Safety and security measures, Stryker Corp. -- Product defects and recalls -- Laws, regulations and rules -- Safety and security measures, Medical equipment -- Product defects and recalls -- Safety and security measures, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Physiological apparatus -- Product defects and recalls -- Safety and security measures, Government regulation, Science and technology
Abstract

OEMs rethink the number of suppliers they use amid increased federal scrutiny. The greatest lessons in life are not always the most evident. Often, they are hidden in great challenges, [...]

Published
2009

46. BD Announces Voluntary Recall of ChloraPrep(TM) 3 mL Applicator in Specific U.S. Territories and Countries

Subjects
Becton, Dickinson and Co. -- Product defects and recalls, High technology industry, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, General interest, News, opinion and commentary
Abstract

FRANKLIN LAKES, New Jersey, Aug. 7, 2020 /PRNewswire-HISPANIC PR WIRE/ --BD (Becton, Dickinson and Company), a leading global medical technology company, announced a voluntary recall on June 23, 2020 for [...]

Published
2020

47. ICU Medical Issues a Voluntary Nationwide Recall of Lactated Ringer's Injection, USP Due to the Presence of Particulate Matter

Subjects
United States. Food and Drug Administration, ICU Medical Inc. -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Business, News, opinion and commentary
Abstract

LAKE FOREST, Ill., May 8, 2020 /PRNewswire/ -- ICU Medical, Inc. is voluntarily recalling one single lot of Lactated Ringer's Injection, USP. The products are being recalled to the hospital/user [...]

Published
2020

48. Medtronic announces voluntary recall of diabetes infusion sets

Subjects
Medtronic PLC -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Intravenous therapy -- Equipment and supplies, Business, News, opinion and commentary
Abstract

Medtronic announced that it has started to inform patients worldwide of a voluntary recall of specific lots of infusion sets used with all models of Medtronic insulin pumps. The recall [...]

Published
2017

49. 2005 medical device recalls and field corrections--year in review

Author

Thomas, Rebecca

Subjects
Defibrillators -- Product defects and recalls, Product recalls -- Forecasts and trends, Product recalls -- Reports, Medical equipment and supplies industry -- Product defects and recalls, Medical equipment and supplies industry -- Industry forecasts, Medical test kit industry -- Product defects and recalls, Medical test kit industry -- Industry forecasts, Medical equipment -- Product defects and recalls, Physiological apparatus -- Product defects and recalls, Product recall, Market trend/market analysis, Business, Health care industry
Published
2006

50. Keeping track of patients and their implants: England and Australia methodically track artificial joints. The U.S. is launching a registry. And Canada?

Author

Lunau, Kate

Subjects
DePuy Orthopaedics Inc. -- Product defects and recalls, Registries (in medicine) -- Information management, Prosthesis -- Product defects and recalls, Medical test kit industry -- Product defects and recalls, Implants, Artificial -- Product defects and recalls, Medical equipment and supplies industry -- Product defects and recalls, Company systems management, General interest, News, opinion and commentary
Abstract

ON THE EVENING of Aug. 27, Lincoln Bryant, a Presbyterian minister in Kingston, Ont., was watching the news. A report came on that left him stunned: DePuy Orthopaedics Inc., a [...]

Published
2010

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