Bieffe Medital Manufacturing S.a.r.l. Tunis
FDA adverse event reports naming Bieffe Medital Manufacturing S.a.r.l. Tunis as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BIEFFE MEDITAL MANUFACTURING S.A.R.L. TUNIS.
- Total reports
- 1,874
- Deaths
- 0
- Injuries
- 7
- Malfunctions
- 1,867
Reports per year
2010
32711
11512
15713
27114
81215
16416
817
Source: FDA adverse event reports by year received, 2010–2017. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Set, Administration, IntravascularFPA1,228
- System, Irrigation, UrologicalLJH567
- Set, Blood TransfusionBRZ51
- Stopcock, I.V. SetFMG12
- Set, I.V. Fluid TransferLHI6
- Set, Administration, For Peritoneal Dialysis, DisposableKDJ4
- Pump, InfusionFRN3
- System, Peritoneal, Automatic DeliveryFKX2
- Dialyzer, High Permeability With Or Without Sealed Dialysate SystemKDI1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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