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Biomet, Inc. recalls Biomet ONPOINT SCOPE PROCEDURE KIT-EU Item Number: 24-3055
Recalled October 14, 2020 · FDA recall Z-0083-2021 · Biomet
Hazard
Product not properly being aligned with the adequate gamma sterilization group and result in the product not being properly sterilized · FDA Class II
Units
US: 33 units; OUS: 269 units
Sold at
Nationwide Foreign: Canada, FINLAND, NETHERLANDS, UNITED KINGDOM
Description
Product not properly being aligned with the adequate gamma sterilization group and result in the product not being properly sterilized
Product
Biomet ONPOINT SCOPE PROCEDURE KIT-EU Item Number: 24-3055
Manufacturer(s)
Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →