BD Vacutainer Push Button Blood Collection Set — Class II medical device recall Z-2710-2016
Terminated recall by Becton Dickinson & Company, reported 2016-09-07. Becton Dickinson is recalling various lot numbers of BD Vacutainer Push Button Blood Collection Set because of
| Recall number | Z-2710-2016 |
|---|---|
| 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 | 2016-08-08 |
| Classified | 2016-09-01 |
| Reported by FDA | 2016-09-07 |
| Terminated | 2017-11-20 |
| Quantity | 1,788,150 units |
| Lot numbers | 5355531, 5355533, 5356681, 5356682, 6006629, 6006630, 6006631, 6006633, 6006634, 6006650 |
| Model numbers | 367342 |
Product
BD Vacutainer Push Button Blood Collection Set, Sterile, Rx only, 0.6 x 19 mm x 305 mm, 23G x 3/4" x 12", REF 367342.
Reason for recall
Becton Dickinson is recalling various lot numbers of BD Vacutainer Push Button Blood Collection Set because of reports that specific lots exhibit separation of fron and rear barrels upon activation of the safety feature, which retracts the needle.
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-2710-2016. 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.