United States Surgical Corp
FDA adverse event reports naming United States Surgical Corp as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: UNITED STATES SURGICAL CORP.
- Total reports
- 3,493
- Deaths
- 9
- Injuries
- 378
- Malfunctions
- 3,093
Reports per year
395
11196
64397
1,37798
51699
58200
22301
502
2303
704
105
110
111
Source: FDA adverse event reports by year received, 1995–2011. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Laparoscope, General & Plastic SurgeryGCJ1,774
- Stapler, SurgicalGAG1,389
- Suture, Nonabsorbable, Synthetic, PolypropyleneGAW94
- Suture, Absorbable, SyntheticGAN35
- Applier, Surgical, ClipGDO33
- TrocarDRC31
- Instrument, Ultrasonic SurgicalLFL31
- Suture, Absorbable, Synthetic, Polyglycolic AcidGAM18
- Suture, Nonabsorbable, SilkGAP13
- Product code KOGKOG12
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor United States Surgical Corp automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.