C.R. Bard, Inc. (covington) -1018233
FDA adverse event reports naming C.R. Bard, Inc. (covington) -1018233 as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: C.R. BARD, INC. (COVINGTON) -1018233.
- Total reports
- 47,290
- Deaths
- 30
- Injuries
- 7,559
- Malfunctions
- 39,695
Reports per year
3312
35513
3214
6415
17016
3,58217
4,74118
6,09019
6,13720
6,57121
7,02622
5,77923
4,03324
2,66825
726
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Catheter, Urological (Antimicrobial) And AccessoriesMJC10,871
- Catheter, UrologicalKOD8,644
- Catheter, CoudeEZC7,960
- Catheter, Retention Type, BalloonEZL3,675
- Catheter, StraightEZD2,341
- Collector, Urine, Powered, Non Indwelling CatheterNZU1,852
- Stent, UreteralFAD1,271
- Collector, Urine, (And Accessories) For Indwelling CatheterKNX1,261
- Holder, Ureteral CatheterEYJ1,072
- Apparatus, Suction, Single Patient Use, Portable, NonpoweredGCY883
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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