BD Caribe Ltd.
FDA adverse event reports naming BD Caribe Ltd. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BD CARIBE LTD..
- Total reports
- 1,249
- Deaths
- 1
- Injuries
- 70
- Malfunctions
- 1,178
Reports per year
915
416
5817
27118
20119
10620
7821
10522
10623
17324
13425
426
Source: FDA adverse event reports by year received, 2015–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Tubes, Vials, Systems, Serum Separators, Blood CollectionJKA973
- Tubes, Vacuum Sample, With AnticoagulantGIM113
- Needle, Conduction, Anesthetic (W/Wo Introducer)BSP87
- Anesthesia Conduction KitCAZ20
- Single Use Only Blood Lancet With An Integral Sharps Injury Prevention FeatureFMK19
- Catheter And Tube, SuprapubicFEZ10
- Needle, Hypodermic, Single LumenFMI8
- Container, Liquid Medication, GraduatedKYW5
- Instrument, Manual, Surgical, General UseMDM5
- Bottle, Collection, VacuumKDQ3
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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