FDAMarch 19, 2021device

Univation X System knee implant devices as follows: Catalog/Product: NO180Z AS UNIVATION XF FEMUR CEMENTED F1 RM; NO181Z AS UNIVATION XF FEMUR CEMENTED F2 RM; NO182Z AS UNIVATION XF FEMUR CEMENTED F3 RM; NO183Z AS UNIVATION XF FEMUR CEMENTED F4 RM; NO184Z AS UNIVATION XF FEMUR CEMENTED F5 RM; NO1...

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

The hazard

Malfunction- loosening of the implant resulting in a potential revision surgery

What to do

FDA enforcement status: Terminated

Brands named

aesculap implant systemsaesculapaesculap implant

Recall history

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

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Univation X System knee implant devices as follows: Catalog/Product: NO180Z AS UNIVATION XF FEMUR CEMENTED F1 RM; NO181Z AS UNIVATION XF FEMUR CEMENTED F2 RM; NO182Z AS UNIVATION XF FEMUR CEMENTED F3 RM; NO183Z AS UNIVATION XF FEMUR CEMENTED F4 RM; NO184Z AS UNIVATION XF FEMUR CEMENTED F5 RM; NO1... — Recall Details · AllClear