BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached… — Class II medical device recall Z-0193-2020
Terminated recall by Becton Dickinson & Company, reported 2019-10-30, distributed nationwide. Separation of front and rear barrels upon activation of the safety feature that retracts the needle
| Recall number | Z-0193-2020 |
|---|---|
| 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 | 2019-07-31 |
| Classified | 2019-10-24 |
| Reported by FDA | 2019-10-30 |
| Terminated | 2020-07-27 |
| Distributed | Nationwide (US) |
| Countries outside the US | HK, TT |
| Quantity | 1,735,600 units |
| Serial numbers | 9079767, 9079770, 9081829, 9086811, 9086812, 9091607, 9091626, 9094659, 9094661, 9098547, 9100711, 9100712, 9115913, 9115965 |
| Model numbers | 368356 |
Product
BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder Catalog number 368356 - Product Usage: This product is designed to provide customers an increased level of safety during IV blood collection, convenience and to improve OSHA single-use holder compliance. Figure 1 shows a BD Vacutainer¿ Push Button Blood Collection Set with the needle protector removed prior to needle retraction.
Reason for recall
Separation of front and rear barrels upon activation of the safety feature that 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-0193-2020. 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.