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

Recall Z-2010-2025 — Brand Name: ALTIVATE REVERSE Product Name: ALTIVATE REVERSE TORX PERIPHERAL SCREW, 18mm Model/Catalog Number: 506-04-118 Software Version: NA Product Description: Encore Medical L.P. shoulder devices are intended for treatment of patients who are candidates for shoulder arthroplasty per the Indi

U.S. FDA — Device Enforcement · United States · 2025-05-28 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2010-2025
Date of alert: 2025-05-28
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Encore Medical, LP
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00190446829836

Reported risk: Package labeling for Altivate Reverse Torx Peripheral screw contains a different size then actual included product.

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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