Recall Z-0083-2021— Biomet, Inc.
Class II · Terminated
Class II FDA medical device recall by Biomet, Inc., initiated 2020-09-04, terminated 2021-08-31. FDA's recall record names no specific 510(k) clearance for this event. Product: Biomet ONPOINT SCOPE PROCEDURE KIT-EU Item Number: 24-3055. Reason: Product not properly being aligned with the adequate gamma sterilization group and result in the product not being properly sterilized.
- Recalling firm
- Biomet, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2020-09-04
- Terminated
- 2021-08-31
- Firm location
- Warsaw, IN, United States
Product description
Biomet ONPOINT SCOPE PROCEDURE KIT-EU Item Number: 24-3055
Reason for recall
Product not properly being aligned with the adequate gamma sterilization group and result in the product not being properly sterilized
Data sourced from openFDA. This site is unofficial and independent of the FDA.