Official recall notice

FDA DeviceClass IINotable

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

Recall date
2026-03-18
FDA class
Class II

Why it was recalled

Hazard

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

Recommended action

What to do

204,000 units

Product description

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

Verify with the official notice →
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