Zimmer Biomet, Inc. recalls Various temporary devices used during the implantation of th
Recalled 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
Hazard / Issue
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
Issued by
FDA
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