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

Recall Z-2527-2015 — Mahurkar Acute Dual Lumen Catheter Tray, High Flow¿ Pre-Curved with IC* Safety Components, 13.5 FR x 13.5 cm Item Code: 8888135139 Product Usage: Sterile Delivery are indicated for use in flushing compatible intravenous administration sets and indwelling intravascular access devices.

U.S. FDA — Device Enforcement · United States · 2015-08-06 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2527-2015
Date of alert: 2015-08-06
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Covidien LLC
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 1506500122

Reported risk: Sterility may be compromised

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

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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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