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

Recall Z-2394-2012 — 0.9% Sodium Chloride Injection, USP, Pre-Filled Flush Solution, 10 mL in 12 mL Single Use Syringe, Rx only, List no. 1078-20, made in Nashville, TN, manufactured for Hospira, Inc., Lake Forest, IL 60045 USA. Flush syringe.

U.S. FDA — Device Enforcement · United States · 2012-08-15 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2394-2012
Date of alert
2012-08-15
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Amsino Medical USA
Product category
device
Product type
Devices
Reported risk: One lot of 0.9% Sodium Chloride Flush syringe, 3 mL in 12 mL may be mislabeled as 0.9% Sodium Chloride Flush syringe, 10 mL in 12 mL.
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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