Biomet ONPOINT SCOPE PROCEDURE KIT-EU Item Number: 24-3055
Reported: October 14, 2020 Initiated: September 4, 2020 #Z-0083-2021
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
Details
- Recalling Firm
- Biomet, Inc.
- Units Affected
- US: 33 units; OUS: 269 units
- Distribution
- Nationwide Foreign: Canada, FINLAND, NETHERLANDS, UNITED KINGDOM
- Location
- Warsaw, IN
Frequently Asked Questions
What product was recalled? ▼
Biomet ONPOINT SCOPE PROCEDURE KIT-EU Item Number: 24-3055. Recalled by Biomet, Inc.. Units affected: US: 33 units; OUS: 269 units.
Why was this product recalled? ▼
Product not properly being aligned with the adequate gamma sterilization group and result in the product not being properly sterilized
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 14, 2020. Severity: Moderate. Recall number: Z-0083-2021.
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