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

Recall Z-2007-2019 — 3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573

U.S. FDA — Device Enforcement · United States · 2019-02-01 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2007-2019
Date of alert
2019-02-01
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Becton Dickinson & Company
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
30382903096573
Reported risk: The syringes have scale markings that were printed incorrectly. The scale is skewed to varying degrees, resulting in missing and/or partially printed scale numbers and scale lines.
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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