FDAJanuary 31, 2025device

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...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The forceps have been used in ways not covered by the design resulting in breakage of the clamps.

What to do

FDA enforcement status: Ongoing

Brands named

aesculap

UPCs

04038653027026040386531392000403865302703304038653027040040386530270570403865302706404038653027071

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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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... — Recall Details · AllClear