medical Class II Updated 2020-10-14

Biomet, Inc. recalls Biomet ARTHROSIMPLICITY KIT EU Item Number: 24-4055

Recalled Product

Biomet ARTHROSIMPLICITY KIT EU Item Number: 24-4055


Hazard / Issue

Product not properly being aligned with the adequate gamma sterilization group and result in the product not being properly sterilized

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot Numbers: 894660A 894660B 894670B 894700B
View official government recall

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