BD Vacutainer Multiple Sample and Direct Draw Luer Adapter BD… — Class II medical device recall Z-1923-2013
Terminated recall by Becton Dickinson & Company, reported 2013-08-14, distributed nationwide. BD Vacutainer Multiple Sample and Direct Draw Luer Adapter may have blood leakage and low draw volume.
| Recall number | Z-1923-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Becton Dickinson & Company, Franklin Lakes, NJ, United States |
| Recall initiated | 2013-05-01 |
| Classified | 2013-08-07 |
| Reported by FDA | 2013-08-14 |
| Terminated | 2015-12-04 |
| Distributed | Nationwide (US) |
| Quantity | 37,906,400 units |
| Reason classes | packaging |
| Model numbers | 367290, 367300 |
Product
BD Vacutainer Multiple Sample and Direct Draw Luer Adapter BD Franklin Lakes, NJ 07417 USA A sterile non-invasive device used to connect venous access devices such as needles, blood collection sets, ad infusion sets to blood collection tubes.
Reason for recall
BD Vacutainer Multiple Sample and Direct Draw Luer Adapter may have blood leakage and low draw volume.
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-1923-2013. 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.