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

Recall Z-2111-2018 — Alaris Extension Sets with microbore tubing Model 20022 and 30914 Is used to administer fluid and medications from a syringe to the patient through a needle or catheter inserted into the patient's artery or vein. These model codes are extension sets that can be used with IV administration sets.

U.S. FDA — Device Enforcement · United States · 2017-11-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2111-2018
Date of alert
2017-11-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
CareFusion 303, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
16087775
Reported risk: Reports of incorrect priming volume due to manufacturing with incorrect tubing.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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