Exactech, Inc.: Medical Device Recall in 2020 - (Recall #: Z-0460-2021)

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 314-13-33, Equinoxe Cage Glenoid, Posterior Augment, Right, Medium

Product Classification:

Class II

Date Initiated: October 6, 2020

Date Posted: November 25, 2020

Recall Number: Z-0460-2021

Event ID: 86630

Reason for Recall:

The product may be mislabeled.

Status: Terminated

Product Quantity: 40 devices

Code Information:

Catalog 314-13-33, Serial Numbers: 6259572 6259573 6259575 6259577 6259578 6259579 6259583 6259584 6259587 6259588 6259590 6259591 6259592 6259594 6259595 6132993 6132994 6132995 6132996 6132997 6132998 6132999 6133000 6133002 6133003 6133005 6133008 6133009 6133010 6133011 6133013 6133014 6133017 6133020 6133021 6133023 6133029 6133030 6133031 6133032

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