FDA-Device2020-10-14Class II
Biomet OnPoint SCOPE PROCEDURE KIT Item Number: 24-3050
Biomet, Inc.
Hazard
Product not properly being aligned with the adequate gamma sterilization group and result in the product not being properly sterilized
Sold states
Nationwide Foreign: Canada, FINLAND, NETHERLANDS, UNITED KINGDOM
Affected count
80 units US
Manufactured in
56 E Bell Dr, N/A, Warsaw, IN, United States
Products
Biomet OnPoint SCOPE PROCEDURE KIT Item Number: 24-3050
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0082-2021Don't want to check this manually?
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