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Medical Device Recalls in Radiation Oncology: Analysis of US Food and Drug Administration Data, 2002-2015.
- Source :
-
International Journal of Radiation Oncology, Biology, Physics . Jun2017, Vol. 98 Issue 2, p438-446. 9p. - Publication Year :
- 2017
-
Abstract
- <bold>Purpose: </bold>To analyze all recalls involving radiation oncology devices (RODs) from the US Food and Drug Administration (FDA)'s recall database, comparing these with non-radiation oncology device recalls to identify discipline-specific trends that may inform improvements in device safety.<bold>Methods and Materials: </bold>Recall data on RODs from 2002 to 2015 were sorted into 4 product categories (external beam, brachytherapy, planning systems, and simulation systems). Outcomes included determined cause of recall, recall class (severity), quantity in commerce, time until recall termination (date FDA determines recall is complete), and time since 510(k) approval. Descriptive statistics were performed with linear regression of time-series data. Results for RODs were compared with those for other devices by Pearson χ2 test for categorical data and 2-sample Kolmogorov-Smirnov test for distributions.<bold>Results: </bold>There were 502 ROD recalls and 9534 other class II device recalls during 2002 to 2015. Most recalls were for external beam devices (66.7%) and planning systems (22.9%), and recall events peaked in 2011. Radiation oncology devices differed significantly from other devices in all recall outcomes (P≤.04). Recall cause was commonly software related (49% vs 10% for other devices). Recall severity was more often moderate among RODs (97.6% vs 87.2%) instead of severe (0.2% vs 4.4%; P<.001). Time from 510(k) market approval to recall was shorter among RODs (P<.001) and progressively shortened over time. Radiation oncology devices had fewer recalled devices in commerce than other devices (P<.001).<bold>Conclusions: </bold>Compared with other class II devices, RODs experience recalls sooner after market approval and are trending sooner still. Most of these recalls were moderate in severity, and software issues are prevalent. Comprehensive analysis of recall data can identify areas for device improvement, such as better system design among RODs. [ABSTRACT FROM AUTHOR]
- Subjects :
- *CANCER radiotherapy
*MEDICAL device approval
*MEDICAL databases
*TIME series analysis
*RADIATION therapy equipment
*RADIOISOTOPE brachytherapy
*CHI-squared test
*COMMERCIAL product evaluation
*COMPUTER software
*DATABASES
*COMPUTERS in medicine
*NONPARAMETRIC statistics
*ONCOLOGY
*PRODUCT recall
*RADIOTHERAPY
*REGRESSION analysis
*RESEARCH funding
*TIME
*EQUIPMENT & supplies
*STANDARDS
Subjects
Details
- Language :
- English
- ISSN :
- 03603016
- Volume :
- 98
- Issue :
- 2
- Database :
- Academic Search Index
- Journal :
- International Journal of Radiation Oncology, Biology, Physics
- Publication Type :
- Academic Journal
- Accession number :
- 122769252
- Full Text :
- https://doi.org/10.1016/j.ijrobp.2017.02.006