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

Recall Z-0898-2015 — Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 10mL Luer lock syringe; Reorder Number: 4102010 Product Usage: The Needle Pro¿ Edge Safety Hypodermic Needle is intended for injection or aspiration of fluids utilizing a luer lock or luer slip syringe.

U.S. FDA — Device Enforcement · United States · 2014-11-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0898-2015
Date of alert
2014-11-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Smiths Medical ASD, Inc.
Product category
device
Product type
Devices
Reported risk: Needle is not captured in the needle safety sheath in specific lots.
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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