C.R. Bard, Inc. (covington)
FDA adverse event reports naming C.R. Bard, Inc. (covington) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: C.R. BARD, INC. (COVINGTON).
- Total reports
- 5,619
- Deaths
- 0
- Injuries
- 5,501
- Malfunctions
- 61
Reports per year
104
60512
4,93313
3714
3415
117
118
419
120
122
123
Source: FDA adverse event reports by year received, 2004–2023. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Mesh, Surgical, PolymericFTL4,135
- Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally PlacedOTP1,013
- Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or TransobturatorOTN310
- Powered Laser Surgical InstrumentGEX38
- Agent, Bulking, Injectable For Gastro-Urology UseLNM33
- Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Female, Mini-SlingPAH33
- Mesh, Surgical, Synthetic, Urogynecologic, For Apical Vaginal And Uterine Prolapse, Transabdominally PlacedOTO13
- Dilator, Catheter, UreteralEZN10
- Mesh, SurgicalFTM10
- Dislodger, Stone, Basket, Ureteral, MetalFFL6
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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