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

Recall Z-0931-2014 — Trifurcated Extension Set, model no. ME 1224. Trifurcated Extension Set, model no. MP 9230.

U.S. FDA — Device Enforcement · United States · 2014-01-16 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0931-2014
Date of alert
2014-01-16
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
CareFusion 303, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
11066540
Reported risk: CareFusion is recalling the Trifurcated Extension Set, models ME 1224 and MP 9230, because they may have a defect in the trifurcated component that could result in a component leak.
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.

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