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FDA (Device enforcement)Recalled 2025-01-31class ii

Aesculap Inc: Numerous models of nonsterile hemostatic forceps: (1) REF BH198R, Fuchsig Artery Forceps CVD.190MM; (2) REF BH304R, Pean Artery Forceps Straight 140MM; (3) REF BH813R, Artery Forceps Cur

Hazard

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

Details from the source

Reason for recall: The forceps have been used in ways not covered by the design resulting in breakage of the clamps. Distribution: Distribution was made nationwide and to PR. There was also government/military distribution. Foreign distribution was made to Canada, Bermuda, Bahamas, and Qatar. Quantity: 93,714 forceps Lot/code info: GTIN numbers: (1) REF BH198R - 04038653026029; (2) REF BH304R - 04038653026333; (3) REF BH813R - 04038653026968; (4) REF BJ016R - 04038653027163; (5) REF BJ020R - 04038653027200; (6) REF BJ021R - 04038653027217; (7) REF BJ022R - 04038653027224; (8) REF BJ023R - 04038653027231; (9) REF BJ025R - 04038653027255; (10) REF BJ026R - 04038653027262; (11) REF BJ031R - 04038653027279; (12) REF BJ034R - 04038653027309; (13) REF BJ035R - 04038653027316; (14) REF BJ037R - 04046963458201; (15) REF BJ038R - 04046963458218; (16) REF BJ039R - 04046963458225; (17) REF BJ041R - 04038653027323; (18) REF BJ042R - 04038653027330; (19) REF BJ043R - 04038653027347; (20) REF BJ044R - 04038653027354; (21) REF BJ045R - 04038653027361; (22) REF BJ047R - 04038653027378; (23) REF BJ048R - 04038653027385; (24) REF BJ050R - 04038653139224; (25) REF BJ051R - 04038653027392; (26) REF BJ052R - 04038653139231; (27) REF BJ055R - 04038653027408; (28) REF BJ057R - 04038653139248; (29) REF BJ058R - 04038653139255; (30) REF BJ059R - 04038653139262; (31) REF BJ060R - 04038653139279; (32) REF BJ061R - 04038653027415; (33) REF BJ062R - 04038653027422; (34) REF BJ068R - 04038653027446; (35) REF BJ070R - 04038653139293; (36) REF BJ073R - 04046963365202; (37) REF BJ080R - 04038653027453; (38) REF BJ081R - 04038653027460; (39) REF BJ082R - 04038653027477; (40) REF BJ083R - 04038653027484; (41) REF BJ086R - 04038653027491; (42) REF BJ090R - 04038653027507; (43) REF BJ091R - 04038653027514; (44) REF BJ096R - 04038653027521;

UPC codes

04038653026029, 04038653026333, 04038653026968, 04038653027163, 04038653027200, 04038653027217, 04038653027224, 04038653027231, 04038653027255, 04038653027262, 04038653027279, 04038653027309, 04038653027316, 04046963458201, 04046963458218, 04046963458225, 04038653027323, 04038653027330, 04038653027347, 04038653027354, 04038653027361, 04038653027378, 04038653027385, 04038653139224, 04038653027392, 04038653139231, 04038653027408, 04038653139248, 04038653139255, 04038653139262, 04038653139279, 04038653027415, 04038653027422, 04038653027446, 04038653139293, 04046963365202, 04038653027453, 04038653027460, 04038653027477, 04038653027484

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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