FDA-Device2020-11-25Class II
Catalog 314-13-33, Equinoxe Cage Glenoid, Posterior Augment, Right, Medium
Exactech, Inc.
Hazard
The product may be mislabeled.
Sold states
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
Affected count
40 devices
Manufactured in
2320 NW 66th Ct, N/A, Gainesville, FL, United States
Products
Catalog 314-13-33, Equinoxe Cage Glenoid, Posterior Augment, Right, Medium
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0460-2021Don't want to check this manually?
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