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

NCB Straight Narrow Plate, various sizes, Item Nos — recall Z-0331-2020

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

As described by U.S. FDA — Device Enforcement: NCB Straight Narrow Plate, various sizes, Item Nos. 0202267008 0202267010 0202267012 0202267014 0202267016 0202267018

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0331-2020
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
Recall status
Terminated — the recall action is complete and the FDA has closed it
Initiated by
Voluntary: Firm initiated
Distribution
Distributed nationwide.
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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