FDA-Device2012-11-14Class II
CoCr Head, sterile, Rx
Zimmer, Inc.
Hazard
Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product patient labels and product labels with respect to the reference and lot numbers of the product. While the information printed on the product label is correct, the info
Sold states
Nationwide Distribution.
Affected count
1000
Manufactured in
345 E Main St, N/A, Warsaw, IN, United States
Products
CoCr Head, sterile, Rx
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0222-2013Don't want to check this manually?
We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.
Get the Sunday Brief