Aesculap Inc 2025-03-19 Health serious FDA
Health · FDA · Recall #FDA-Z-1312-2025
Numerous models of nonsterile hemostatic forceps: (1) REF BH951R, Negus Tonsil Forceps… Recall
Issued March 19, 2025 · Aesculap Inc
In March 2025, Aesculap Inc recalled the Numerous models of nonsterile hemostatic forceps: (1) REF BH951R, Negus Tonsil Forceps…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
What you should do
- 1 Stop using Numerous models of nonsterile hemostatic forceps: (1) REF BH951R, Negus Tonsil Forceps… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Aesculap Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Aesculap Inc
- Category
- Health
- Recall date
- March 19, 2025
- Units affected
- Not reported
- Sold at
- Distribution was made nationwide and to PR. There was also government/military distribution. Foreign distribution was made to Canada, Be
- Recall number
- FDA-Z-1312-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Aesculap Inc has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.