CLASS II ONGOING Device recall · Reported 24 Sep 2025 · FDA Enforcement Report

Equinoxe, Reverse Shoulder Humeral Liners recalled by Exactech

Exactech is recalling Equinoxe, Reverse Shoulder Humeral Liners, 322-38-00 (145-DEG PE HUM Liner +0), distributed nationwide in the US. The recall was initiated on 15 Aug 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll Serial Numbers, REF: 322-38-00/UDI:10885862593832, REF: 322-38-03/UDI:10885862593849, REF: 322-42-00/UDI: 10885862593917, REF:322-42-03/UDI:10885862593924
Quantity recalled11,542 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-2562-2025
FDA event ID
97459
Recalling firm
Exactech, Gainesville, FL
Classification
Class II
Status
Ongoing
Recall initiated
15 Aug 2025
FDA classified
12 Sep 2025
Reported
24 Sep 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Other Reasons

Timeline

15 Aug 2025Recall initiated by company
12 Sep 2025Classified by FDA+28 days
24 Sep 2025Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

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)

Where it was distributed

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.

Nationwide CaliforniaColoradoFloridaGeorgiaHawaiiIdahoIllinoisIndianaKansasKentuckyLouisianaMassachusettsMarylandMaineMinnesotaNevadaNew YorkOhioOklahomaPuerto Rico

Questions about this recall

Why was it recalled?

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

Which lots are affected?

All Serial Numbers, REF: 322-38-00/UDI:10885862593832, REF: 322-38-03/UDI:10885862593849, REF: 322-42-00/UDI: 10885862593917, REF:322-42-03/UDI:10885862593924

Where was it sold?

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.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 97459
ReportedClassRecallCompanyReasonWhere
CLASS IIEquinoxe, Reverse Shoulder Humeral Liners recalled by ExactechExactechOtherNationwide

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