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Zimmer Biomet, Inc. recalls ECHO POR FMRL NC 9X125, model # 192009
Recalled January 10, 2018 · FDA recall Z-0300-2018 · Zimmer Biomet
Hazard
Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and actual product are correctly identified but the internal patient label could be incorrect. · FDA Class II
Units
N/A
Sold at
Nationwide in US; Internationally Argentina, Netherlands & Canada
Description
Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and actual product are correctly identified but the internal patient label could be incorrect.
Product
ECHO POR FMRL NC 9X125, model # 192009
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →