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

Recall Z-1126-2014 — * 1) List number 126970465 labeled in part: 12697-65 LifeShield LATEX-FREE HEMA; Y-TYPE BLOOD SET, Nonvented, 88 Inch with 210 Micron Filter Pump, Prepierced Injection Site and Secure Lock; Made in Costa Rica; Product Inquiries should be directed to Hospira, Inc., Lake Forest, IL 60045 USA;

U.S. FDA — Device Enforcement · United States · 2013-10-25 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1126-2014
Date of alert: 2013-10-25
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Hospira Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 126970465

Reported risk: Several lots of the LifeShield Latex-Free HEMA Y-Type Blood Set IV Administration Set were assembled incorrectly.

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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