Ponce - USS
FDA adverse event reports naming Ponce - USS as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: PONCE - USS.
- Total reports
- 4,250
- Deaths
- 66
- Injuries
- 2,096
- Malfunctions
- 1,948
Reports per year
200
7401
23402
26103
60104
53105
48206
56207
61908
61709
26710
Source: FDA adverse event reports by year received, 2000–2010. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Laparoscope, General & Plastic SurgeryGCJ1,622
- Stapler, SurgicalGAG1,396
- Staple, ImplantableGDW570
- TrocarDRC339
- Applier, Surgical, ClipGDO65
- Suture, Nonabsorbable, Synthetic, PolyesterGAS38
- Product code KOGKOG34
- Dissector, Surgical, General & Plastic SurgeryGDI32
- Gouge, Surgical, General & Plastic SurgeryGDH30
- Staple, Removable (Skin)GDT26
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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