Numerous recall
Numerous models of nonsterile hemostatic forceps: (1) REF BH198R, Fuchsig Artery Forceps CVD.190MM; (2) REF BH304R, Pean Artery Forceps Straight…
Why was Numerous recalled?
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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; (45) REF BJ100R - 04038653027538; (46) REF BJ102R - 04038653027545; (47) REF BJ103R - 04038653027552; (48) REF BJ104R - 04038653027569; (49) REF BJ106R - 04038653027576; (50) REF BJ120R - 04038653027606; (51) REF BJ121R - 04038653027613; (52) REF BJ122R - 04038653027620; (53) REF BJ123R - 04038653027637; (54) REF BJ130R - 04038653256457; (55) REF BJ131R - 04038653256464; (56) REF BJ132R - 04038653256471; (57) REF FB440R - 04038653155897; (58) REF FB441R - 04038653155903; (59) REF FB442R - 04038653155910; (60) REF FB443R - 04038653155927; (61) REF FB446R - 04038653155958; (62) REF FB447R - 04038653155965; (63) REF FB448R - 04038653155972; (64) REF FB483R - 04038653156306; (65) REF FB486R - 04038653156337; (66) REF FB487R - 04038653156344; (67) REF FB496R - 04038653156436; (68) REF FB498R - 04038653156450; (69) REF FB499R - 04038653156467; (70) REF FB526R - 04038653156719; (71) REF FB527R - 04038653156726; (72) REF FB533R - 04038653156771; (73) REF FB534R - 04038653156788; (74) REF FB563R - 04038653156931; (75) REF FB570R - 04038653156979; (76) REF FB741R - 04038653157716; (77) REF FB961R - 04038653158560; (78) REF MD465R - 04038653379507; (79) REF MD466R - 04038653379521; (80) REF MD467R - 04038653379545; (81) REF MD468 - 04046963366117; (82) REF MD569 - 04046963365578; and (83) REF MD570R - 04038653394999.
- Product
- Numerous models of nonsterile hemostatic forceps: (1) REF BH198R, Fuchsig Artery Forceps CVD.190MM; (2) REF BH304R, Pean Artery Forceps Straight…
- Recalling firm
- Aesculap Inc
- Quantity
- 93,714 forceps
- Distribution
- Distribution was made nationwide and to PR. There was also government/military distribution. Foreign distribution was made to Canada, Bermuda, Bahamas, and Qatar.
- Recall date
- March 19, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)