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Exactech, Inc. recalls Catalog 314-13-33, Equinoxe Cage Glenoid, Posterior Augment, Right, Medium
Recalled November 25, 2020 · FDA recall Z-0460-2021 · Exactech
Hazard
The product may be mislabeled. · FDA Class II
Units
40 devices
Sold at
US consignees - AZ, CA, CO, FL, IL, IN, KY, LA, OH, OK, MD, ME, MN, NV, NY, SC, TN, TX, VA, WA, WI International consignees - Australia, Japan, and United Kingdom
Description
The product may be mislabeled.
Product
Catalog 314-13-33, Equinoxe Cage Glenoid, Posterior Augment, Right, Medium
Manufacturer(s)
Exactech, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →