[Recalled] 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 vit
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| 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. |
|---|---|
| Brand / manufacturer | Fresenius Medical Care Holdings, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2629-2014 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 23 June 2014 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Products were held at improper storage temperature
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
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This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.