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
- 22,428
- Deaths
- 34
- Injuries
- 2,433
- Malfunctions
- 19,959
Reports per year
1,86617
2,31918
2,55319
1,87720
2,02121
2,00022
2,31323
2,69924
2,62325
2,15726
Source: FDA adverse event reports by year received, 2017–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Suture, Absorbable, Synthetic, Polyglycolic AcidGAM6,453
- Clip, ImplantableFZP4,370
- Laparoscope, General & Plastic SurgeryGCJ3,912
- Endoscopic Tissue Approximation DeviceOCW1,753
- Suture, Nonabsorbable, Synthetic, PolypropyleneGAW1,695
- Laryngoscope, EndoscopeGCI979
- Suture, Nonabsorbable, Synthetic, PolyamideGAR560
- Product code KOGKOG476
- Suture, Nonabsorbable, Synthetic, PolyethyleneGAT450
- Staple, ImplantableGDW409
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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