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Aesculap Inc recalls Numerous models of nonsterile hemostatic forceps: (1) REF BH951R, Negus Tonsil Forceps HVY-CVD 190MM; (2) REF BH952R
Recalled March 19, 2025 · FDA recall Z-1312-2025 · Aesculap
Hazard
The forceps have been used in ways not covered by the design resulting in breakage of the clamps. · FDA Class II
Units
47,078 forceps
Sold at
Distribution was made nationwide and to PR. There was also government/military distribution. Foreign distribution was made to Canada, Bermuda, Bahamas, and Qatar.
Description
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Product
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.
Manufacturer(s)
Aesculap Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →