FDA Medical devices recall ·
10mL Non-Sterile BD Luer-Lok Tip Syringe Only recall
- Recall number
- Z-1496-2026
- Date
- (initiated January 27, 2026)
- Company / brand
- Becton Dickinson & Co.
1 Becton Dr, Franklin Lakes, NJ, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 204,000 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.
Why was it recalled?
During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Catalog Number: 301029., UDI-DI: N/A. Lot Number: 5268614. Expiration Date: 08/31/2030.
Distribution
US Nationwide distribution in the states of California and Texas.
States: California Texas
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1496-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.