Home / Recalls / Medical Devices
Biomet, Inc. recalls Biomet OnPoint SCOPE PROCEDURE KIT Item Number: 24-3050
Recalled October 14, 2020 · FDA recall Z-0082-2021 · 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
80 units US
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 Item Number: 24-3050
Manufacturer(s)
Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →