BD 23 G x — Class II medical device recall Z-0745-2017
Ongoing recall by Becton Dickinson & Company, reported 2016-12-21, distributed nationwide. BD has received multiple reports of units associated with the 23 G x .75 in. BD Vacutainer¿ Push Button Blood
| Recall number | Z-0745-2017 |
|---|---|
| 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 | 2016-08-08 |
| Classified | 2016-12-12 |
| Reported by FDA | 2016-12-21 |
| Distributed | Nationwide (US) |
| Countries outside the US | BE, BR, CA |
| Quantity | 1,788,150 units |
| Model numbers | 367342 |
Product
BD 23 G x .75 in. BD Vacutainer¿ Push Button Blood Collection Set with 12 in. Tubing Catalog # 367342 Intended for venipuncture to obtain blood specimens from patients.
Reason for recall
BD has received multiple reports of units associated with the 23 G x .75 in. BD Vacutainer¿ Push Button Blood Collection Set with 12 in. Tubing whose lots are exhibiting separation of front 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-0745-2017. 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.