Exactech, Inc.: Medical Device Recall in 2020 - (Recall #: Z-0459-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Catalog 314-13-23, Equinoxe Cage Glenoid, Posterior Augment, Left, Medium

Product Classification:

Class II

Date Initiated: October 6, 2020

Date Posted: November 25, 2020

Recall Number: Z-0459-2021

Event ID: 86630

Reason for Recall:

The product may be mislabeled.

Status: Terminated

Product Quantity: 69 devices

Code Information:

Catalog 314-13-23, Serial Numbers: 6262746 6262747 6262748 6262749 6262750 6262751 6262753 6262754 6262756 6262757 6262758 6262759 6262760 6262761 6262762 6262763 6142776 6142777 6142779 6142780 6142782 6142783 6142785 6142787 6142788 6142790 6142792 6142793 6142794 6142795 6142796 6142798 6142801 6142802 6142803 6142804 6130334 6130335 6130336 6130340 6130341 6130343 6130344 6130347 6130352 6130353 6130355 6130356 6130357 6130358 6130361 6130365 6130366 6130367 6130368 6147287 6147294 6147297 6147298 6147299 6147300 6147301 6147303 6147303 6147308 6147310 6147314 6147317 6147318

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated