BD Vacutainer Serum Tubes — Class II medical device recall Z-2629-2014
Terminated recall by Fresenius Medical Care Holdings, Inc., reported 2014-09-24, distributed in LA, OK, TX. Products were held at improper storage temperature
| Recall number | Z-2629-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Fresenius Medical Care Holdings, Inc., Waltham, MA, United States |
| Recall initiated | 2014-06-23 |
| Classified | 2014-09-12 |
| Reported by FDA | 2014-09-24 |
| Terminated | 2021-01-29 |
| Distributed | LA, OK, TX |
| Quantity | 3 boxes |
| Lot numbers | 3319877 |
| Model numbers | 367815FMC, 87-7815-4 |
Product
BD Vacutainer Serum Tubes (RED TOP PLAIN TUBE 6.0 ML)Part Number: BD 367815 FMC Part Number: 87-7815-4 Single use tube used to collect, separate, transport or process blood specimens for laboratory determinations for in vitro diagnostic use.
Reason for recall
Products were held at improper storage temperature
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-2629-2014. 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.