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

Recall Z-2533-2015 — Mahurkar Elite Acute Triple Lumen Catheter Tray, Curved Extensions with IC* Safety Components, 12.5 Fr x 13 cm Item Code: 8888233413 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-2533-2015
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)
1504700136
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.