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BD 10mL Non-Sterile Luer-Lok Syringe
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MEDICAL DEVICE RECALLMODERATE

BD 10mL Non-Sterile Luer-Lok Syringe

BD is recalling 10mL non-sterile Luer-Lok syringes (catalog 301029) due to incorrect Luer Slip syringes mixed into batches.

What to do

Stop using the affected syringes immediately. Check your inventory for catalog number 301029 and verify the Luer Lok connection type. Contact Becton Dickinson for instructions on return or replacement of affected units.

Recalled
Listed
Updated
Recall No.
Z-1496-2026
Agency
FDA
Firm
Becton Dickinson & Company
Recall ID
98314
Status
ONGOING

Recall at a glance

Quantity recalled
204,000 units

Why it was recalled

Becton Dickinson is recalling 10mL non-sterile BD Luer-Lok tip syringes (catalog number 301029, 850 units per case) because some Luer Slip syringes were incorrectly included in batches designated for Luer Lok syringes during bulk packaging. The products were distributed nationwide in California and Texas.

Is mine affected?

This recall covers the product below. If you have it, yours is affected.

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

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

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Editorial summary by Recall Canary · summary updated 2026-04-27 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification