10mL Non-Sterile BD Luer-Lok Tip Syringe Only — Class II medical device recall Z-1496-2026
Ongoing recall by Becton Dickinson & Company, reported 2026-03-18, distributed nationwide. During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for
| Recall number | Z-1496-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Becton Dickinson & Company, Franklin Lakes, NJ, United States |
| Recall initiated | 2026-01-27 |
| Classified | 2026-03-06 |
| Reported by FDA | 2026-03-18 |
| Distributed | Nationwide (US) |
| Quantity | 204,000 units |
| Lot numbers | 5268614 |
| Model numbers | 301029, 850 |
| Expiration dates | 2030-08-31 |
Product
10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.
Reason for recall
During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1496-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.