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Biomet, Inc. recalls RapidFire Clip, Item Number 95-0154 - Product Usage: Fixation of Craniofacial bone.
Recalled December 23, 2020 · FDA recall Z-0626-2021 · Biomet
Hazard
Specific lots of multiple sterile medical devices may have a breach in the sterile seal. A breach in the packaging seal could lead to loss of sterility of the device. · FDA Class II
Units
7428
Sold at
Worldwide distribution. US nationwide, ARGENTINA, AUSTRALIA, Brazil, CANADA, CHILE, CHINA, COSTA RICA, EMEA, HONG KONG, INDIA, JAPAN, KOREA, MALAYSIA, NEW ZEALAND, SINGAPORE, and TAIWAN
Description
Specific lots of multiple sterile medical devices may have a breach in the sterile seal. A breach in the packaging seal could lead to loss of sterility of the device.
Product
RapidFire Clip, Item Number 95-0154 - Product Usage: Fixation of Craniofacial bone.
Manufacturer(s)
Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →