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
- 12,601
- Deaths
- 40
- Injuries
- 1,296
- Malfunctions
- 11,188
Reports per year
392
993
10894
8395
1,58196
4,84597
2,56898
1,83399
1,38200
15601
102
1103
904
1205
Source: FDA adverse event reports by year received, 1992–2005. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Laparoscope, General & Plastic SurgeryGCJ6,595
- Stapler, SurgicalGAG3,804
- Suture, Absorbable, SyntheticGAN524
- Suture, Absorbable, Synthetic, Polyglycolic AcidGAM351
- Applier, Surgical, ClipGDO268
- Suture, Nonabsorbable, Synthetic, PolypropyleneGAW229
- Instrument, Ultrasonic SurgicalLFL127
- Suture, Absorbable, NaturalGAL100
- Suture, Nonabsorbable, SilkGAP76
- Port & Catheter, Implanted, Subcutaneous, IntravascularLJT70
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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