Ethicon, Inc. SAN Angelo
FDA adverse event reports naming Ethicon, Inc. SAN Angelo as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ETHICON, INC. SAN ANGELO.
- Total reports
- 1,110
- Deaths
- 9
- Injuries
- 986
- Malfunctions
- 112
Reports per year
3398
16199
13100
38501
22302
12103
5504
113
Source: FDA adverse event reports by year received, 1998–2013. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Suture, Absorbable, Synthetic, Polyglycolic AcidGAM857
- Suture, Absorbable, SyntheticGAN201
- Suture, Nonabsorbable, Synthetic, PolypropyleneGAW17
- Suture, NonabsorbableGAO11
- Instrument, Manual, Surgical, General UseMDM9
- Suture, Nonabsorbable, Synthetic, PolyesterGAS5
- Mesh, Surgical, PolymericFTL4
- Suture, Absorbable, NaturalGAL2
- Suture, Nonabsorbable, Synthetic, PolyethyleneGAT1
- Laparoscope, General & Plastic SurgeryGCJ1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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