Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Numerous models of nonsterile hemostatic forceps: (1) REF BH951R Recalled by Aesculap Inc Due to The forceps have been used in ways not...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Aesculap Inc directly.
Affected Products
Numerous models of nonsterile hemostatic forceps: (1) REF BH951R, Negus Tonsil Forceps HVY-CVD 190MM; (2) REF BH952R, Negus Tonsil Forceps X-HVY-CVD190MM; (3) REF BH957R, Schnidt Tonsil Forceps SLT-CVD185MM; (4) REF BH959R, Schnidt Tonsil Forceps CVD 185MM; (5) REF BH961R, Schnidt Tonsil FCPSOPEN-RINGCVD 185MM; (6) REF BH963R, Schnidt Tonsil FCPSOPEN-RINGCVD185MM; and (7) REF BH965R, Wilson Tonsil Forceps 190MM.
Quantity: 47,078 forceps
Why Was This Recalled?
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Aesculap Inc
Aesculap Inc has 18 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report