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

Recall Z-1201-2026 — Brand Name: Zimmer Tourniquet Systems Product Name: A.T.S.¿ 5000TS Tourniquet Systems Model/Catalog Number: 60500010100 Software Version: Software version v2.04 or prior are within scope of the recall for A.T.S.¿ 5000TS Product Description: A.T.S 5000TS Tourniquet Systems Component: N/A

U.S. FDA — Device Enforcement · United States · 2025-12-24 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1201-2026
Date of alert: 2025-12-24
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Zimmer Surgical Inc
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 60500010100

Reported risk: Device user interface (screen) may freeze or become unresponsive to touch when operating in certain non-English language settings. Issue may cause delay or extension while alternate device is located.

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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