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
- 12,851
- Deaths
- 7
- Injuries
- 1,416
- Malfunctions
- 11,428
Reports per year
321
522
52823
1,49024
6,81025
4,01526
Source: FDA adverse event reports by year received, 2021–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Catheter, Urological (Antimicrobial) And AccessoriesMJC4,664
- Collector, Urine, Powered, Non Indwelling CatheterNZU1,878
- Catheter, CoudeEZC1,620
- Catheter, UrologicalKOD1,307
- Catheter, Retention Type, BalloonEZL1,291
- Stent, UreteralFAD330
- Collector, Urine, (And Accessories) For Indwelling CatheterKNX284
- Tubes, Gastrointestinal (And Accessories)KNT224
- Apparatus, Suction, Single Patient Use, Portable, NonpoweredGCY196
- Catheter, IrrigationGBX179
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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