Reported Mar 19, 2025 · Ongoing
Numerous models of nonsterile hemostatic forceps
Aesculap Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Aesculap Inc · 3773 Corporate Pkwy · Center Valley, PA · 18034-8217
Is this the product you have?
Numerous models of nonsterile hemostatic forceps
7 of 7 products
| Model / number | Product as published |
|---|---|
BH951R | (1) , Negus Tonsil Forceps HVY-CVD 190MM |
BH952R | (2) , Negus Tonsil Forceps X-HVY-CVD190MM |
BH957R | (3) , Schnidt Tonsil Forceps SLT-CVD185MM |
BH959R | (4) , Schnidt Tonsil Forceps CVD 185MM |
BH961R | (5) , Schnidt Tonsil FCPSOPEN-RINGCVD 185MM |
BH963R | (6) , Schnidt Tonsil FCPSOPEN-RINGCVD185MM |
BH965R | and (7) , Wilson Tonsil Forceps 190MM. |
- Amount recalled
- 47,078 forceps
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
- Nationwide
- PR
Why it was recalled
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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