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Zimmer Biomet, Inc. recalls ARCOS Modular Revision Hip System, item number 11-300814 orthopedic hip prosthesis femoral stem.
Recalled August 22, 2018 · FDA recall Z-2820-2018 · Zimmer Biomet
Hazard
Two lots of the Echo BI-Metric Hip Stem and ARCOS Modular Revision Hip Stem may have been comingled. Potential health consequences include extension of surgery time to find a replacement component. · FDA Class II
Units
12
Sold at
US distribution to CA, GA, IL, MO, NY, and VA.
Description
Two lots of the Echo BI-Metric Hip Stem and ARCOS Modular Revision Hip Stem may have been comingled. Potential health consequences include extension of surgery time to find a replacement component.
Product
ARCOS Modular Revision Hip System, item number 11-300814 orthopedic hip prosthesis femoral stem.
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →