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

3mL Safety-Lok Syringe, Catalog Number 309606, UDI 30382903096061 — recall Z-2008-2019

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-2008-2019
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)
30382903096061
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.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.