Bard Shannon Limited
FDA adverse event reports naming Bard Shannon Limited as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BARD SHANNON LIMITED.
- Total reports
- 1,592
- Deaths
- 1
- Injuries
- 1,514
- Malfunctions
- 70
Reports per year
309
28012
1,20913
3514
3115
116
418
619
420
521
422
323
424
225
126
Source: FDA adverse event reports by year received, 2009–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Mesh, Surgical, PolymericFTL1,006
- Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or TransobturatorOTN313
- Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally PlacedOTP122
- Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Female, Mini-SlingPAH80
- Mesh, Surgical, Synthetic, Urogynecologic, For Apical Vaginal And Uterine Prolapse, Transabdominally PlacedOTO39
- Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 DaysLJS13
- Tube, Tracheal (W/Wo Connector)BTR5
- Staple, ImplantableGDW5
- Tubes, Gastrointestinal (And Accessories)KNT2
- Instrument, BiopsyKNW2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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