Catalog 314-13-23, Equinoxe Cage Glenoid, Posterior Augment, Left, Medium
Reported: November 25, 2020 Initiated: October 6, 2020 #Z-0459-2021
Product Description
Catalog 314-13-23, Equinoxe Cage Glenoid, Posterior Augment, Left, Medium
Reason for Recall
The product may be mislabeled.
Details
- Recalling Firm
- Exactech, Inc.
- Units Affected
- 69 devices
- Distribution
- 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
- Location
- Gainesville, FL
Frequently Asked Questions
What product was recalled? ▼
Catalog 314-13-23, Equinoxe Cage Glenoid, Posterior Augment, Left, Medium. Recalled by Exactech, Inc.. Units affected: 69 devices.
Why was this product recalled? ▼
The product may be mislabeled.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 25, 2020. Severity: Moderate. Recall number: Z-0459-2021.
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