Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2549-2025 — Brand Name: DJO SURGICAL Product Name: FA S Altivate Reverse Glenoid Tray Model/Catalog Number: None Software Version: NA Product Description: Enovis" shoulder devices are intended for treatment of patients who are candidates for shoulder arthroplasty per the Indication for use. While total shou

U.S. FDA — Device Enforcement · United States · 2025-07-18 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2549-2025
Date of alert: 2025-07-18
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Encore Medical, LP
Product category: device
Product type: Devices

Reported risk: Their is a potential that the reamer may kick or bind up during or immediately prior to use.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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