RecallRadar

FDA Device recall Z-2562-2025

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.…

On 2025-09-24 the FDA classified a Class II recall of 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.… by Exactech, citing reverse Shoulder humeral liners have an articular surface position outside of the dimensional specification within the labeling.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2562-2025
ClassificationClass II
Statusongoing
Initiated2025-08-15
Published2025-09-24
Last updated2026-09-13 11:57 UTC
CompanyExactech
DistributionUS

Product

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

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

Identifiers

code_infoAll 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

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2562-2025%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.