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

Universal Locking Plates Sterile, Item Nos. 47492800207 47492800303 47492800402 47492800403 47492800407 47492800502 47492800503 47492800507 47492800603 47492800607 47492800613 47492800702 47492800703 47492800707 47492800802 47492800803 47492800807 47492800813 47492800902 4749280 — recall Z-0312-2020

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-0312-2020
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): 47492800207

Reported risk: Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).

Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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