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

Recall Z-1356-2020 — Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC, Dual Port, Dual Bladder, Item No. 60708015200, UDI (01)00889024377547 (17)230812(10)27968701 The product is a tourniquet - Product Usage: Tourniquets are intended to be used by qualified medical professionals to exert e

U.S. FDA — Device Enforcement · United States · 2020-01-03 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1356-2020
Date of alert: 2020-01-03
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Zimmer Surgical Inc
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 27968701

Reported risk: When inflating/deflating a single bladder, both bladders could potentially inflate/deflate due to a leak between the bladders.

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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