HomeMedical Device recalls
Medium severity

10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.

SourceFDA Device Enforcement
CategoryMedical Device
SeverityMedium
Statusongoing
Recall dateJanuary 27, 2026
ReportedMarch 18, 2026
Recalling firmBecton Dickinson & Company
Country / regionUnited States NJ

Hazard

During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.

Affected products

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