Davis & Geck Caribe Ltd
FDA adverse event reports naming Davis & Geck Caribe Ltd as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DAVIS & GECK CARIBE LTD.
- Total reports
- 21,685
- Deaths
- 31
- Injuries
- 2,379
- Malfunctions
- 19,275
Reports per year
1,86617
2,31918
2,55319
1,87720
2,02121
2,00022
2,31323
2,69924
2,62325
1,41426
Source: FDA adverse event reports by year received, 2017–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Suture, Absorbable, Synthetic, Polyglycolic AcidGAM6,200
- Clip, ImplantableFZP4,226
- Laparoscope, General & Plastic SurgeryGCJ3,835
- Endoscopic Tissue Approximation DeviceOCW1,728
- Suture, Nonabsorbable, Synthetic, PolypropyleneGAW1,602
- Laryngoscope, EndoscopeGCI949
- Suture, Nonabsorbable, Synthetic, PolyamideGAR542
- Product code KOGKOG476
- Suture, Nonabsorbable, Synthetic, PolyethyleneGAT432
- Staple, ImplantableGDW407
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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