BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x100mm 5 — Class II medical device recall Z-2056-2018
Terminated recall by Becton Dickinson & Company, reported 2018-06-13, distributed nationwide. Tubes may exhibit stopper creepout/pullout, where the stopper dissociates from the tube
| Recall number | Z-2056-2018 |
|---|---|
| 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 | 2018-02-13 |
| Classified | 2018-06-01 |
| Reported by FDA | 2018-06-13 |
| Terminated | 2020-03-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, BR, BZ, CA, CN, IN, JP, MX, NI, PH, PK, SG, TW |
| Quantity | 9,568,900 products |
| UPC / GTIN / UDI-DI | 50382903679862 |
| Serial numbers | 7146901 |
| Model numbers | 367986 |
| Expiration dates | 2018-05-31 |
Product
BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x100mm 5.0ml PLBL Gold, Catalog No. 367986
Reason for recall
Tubes may exhibit stopper creepout/pullout, where the stopper dissociates from the tube
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-2056-2018. 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.