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Zimmer Biomet, Inc. recalls Various temporary devices used during the implantation of the device system: bone fixation plates and screws, drill bits
Recalled November 13, 2019 · FDA recall Z-0329-2020 · Zimmer Biomet
Hazard
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration). · FDA Class II
Units
5,459,583 total devices
Sold at
Distributed nationwide.
Description
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
Product
Various temporary devices used during the implantation of the device system: bone fixation plates and screws, drill bits, manual surgical instruments for general use. Item Nos. 0202024301 0202024325 0202024330 0202024342 0202024344 0202024346 0202024360 0202024362 47225806700
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →