PlainRecalls
FDA Devices Moderate Class II Ongoing

Exactech Equinoxe, Reverse Shoulder Humeral Liners, 322-38-00 (145-DEG PE 38MM HUM LINER +0), REF: 322-38-03 (145-DEG PE 38MM HUM LINER +2.5), REF:322-42-00 (145-DEG PE 42MM HUM LINER +0), REF: 322-42-03 (145-DEG PE 42MM HUM LINER +2.5)

Reported: September 24, 2025 Initiated: August 15, 2025 #Z-2562-2025

Product Description

Exactech Equinoxe, Reverse Shoulder Humeral Liners, 322-38-00 (145-DEG PE 38MM HUM LINER +0), REF: 322-38-03 (145-DEG PE 38MM HUM LINER +2.5), REF:322-42-00 (145-DEG PE 42MM HUM LINER +0), REF: 322-42-03 (145-DEG PE 42MM HUM LINER +2.5)

Reason for Recall

Reverse Shoulder humeral liners have an articular surface position outside of the dimensional specification within the labeling.

Details

Recalling Firm
Exactech, Inc.
Units Affected
11,542 units
Distribution
Worldwide - US Nationwide distribution in the states of CA, CO, FL, GA, HI, ID, IL, IN, KS, KY, LA, MA, MD, ME, MN, NV, NY, OH, OK, PR, SC, TN, TX, VA, WI and the countries of Australia, Austria, Brazil, Canada, Colombia, France, United Kingdom, Guatemala, India, Italy, Japan, Korea, Germany, The Netherlands, Slovenia, South Africa, Spain, Sweden, Switzerland, Thailand, Dubai.
Location
Gainesville, FL

Frequently Asked Questions

What product was recalled?
Exactech Equinoxe, Reverse Shoulder Humeral Liners, 322-38-00 (145-DEG PE 38MM HUM LINER +0), REF: 322-38-03 (145-DEG PE 38MM HUM LINER +2.5), REF:322-42-00 (145-DEG PE 42MM HUM LINER +0), REF: 322-42-03 (145-DEG PE 42MM HUM LINER +2.5). Recalled by Exactech, Inc.. Units affected: 11,542 units.
Why was this product recalled?
Reverse Shoulder humeral liners have an articular surface position outside of the dimensional specification within the labeling.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 24, 2025. Severity: Moderate. Recall number: Z-2562-2025.