FDA recall record

Exactech Equinoxe, Reverse Shoulder Humeral Liners, 322-38-00 recall — FDA Z-2562-2025

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

Class IIclassification
Z-2562-2025official record ID
Sep 24, 2025report date

Recall record at a glance

Official recordZ-2562-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmExactech, Inc.
Report dateSep 24, 2025
Recall initiation dateAug 15, 2025
Quantity11,542 units
LocationGainesville, FL, United States

Official 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)

Why the product was recalled

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

Distribution information

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.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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