Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0329-2020 — 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

U.S. FDA — Device Enforcement · United States · 2019-10-10 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0329-2020
Date of alert
2019-10-10
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zimmer Biomet, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
0202024301
Reported risk: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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