North Haven - USS
FDA adverse event reports naming North Haven - USS as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: NORTH HAVEN - USS.
- Total reports
- 4,065
- Deaths
- 56
- Injuries
- 3,067
- Malfunctions
- 920
Reports per year
500
8401
22702
29003
34104
29805
42106
65107
81508
80309
13010
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
- Stapler, SurgicalGAG1,158
- Staple, ImplantableGDW999
- Laparoscope, General & Plastic SurgeryGCJ560
- Instrument, Ultrasonic SurgicalLFL414
- Device, Endoscopic SuturingMFJ163
- Product code KOGKOG146
- Suture, Absorbable, Synthetic, Polyglycolic AcidGAM123
- Applier, Surgical, ClipGDO118
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI83
- Suture, Absorbable, SyntheticGAN81
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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