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

Recall Z-2062-2016 — *** 1) Product labeled in part: 19683-28; LIFESHIELD; MICRODRIP SOLUSET WITH 1.2 MICRON FILTER 150ML BURETTE PLUMSET, CONVERTIBLE PIN, CLAVE SECONDARY PORT, OPTION-LOK, NON-DEHP; NOMINAL LENGTH: 118 IN; PRIMING VOLUME: 14 ML; *** 2) Product labeled in part: List No. 19685-28; LifeShield; LATEX-FRE

U.S. FDA — Device Enforcement · United States · 2013-09-09 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2062-2016
Date of alert
2013-09-09
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Hospira Inc.
Product category
device
Product type
Devices
Reported risk: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV administration sets.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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