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

Recall Z-0532-2020 — LT DISC ULNA - HA/PC; RT DISC ULNA - HA/PC; LT DISC HMRL- HA/PC; RT DISC HMRL- HA/PC; DISC XS ULNA POR; DISC SEG ULNA POR; and Custom devices Item Nos. 114754 114755 114744 114745 114704 114705 114756 114757 114714 114715 114746 114747 114706 114707 114758 114759 114716 1

U.S. FDA — Device Enforcement · United States · 2019-08-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0532-2020
Date of alert
2019-08-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zimmer Biomet, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00880304436343
Reported risk: Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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