Fresenius Recalls BD Vacutainer Serum Tubes Due to Improper Storage Temperature
Fresenius Medical Care is recalling 3 boxes of BD Vacutainer Serum Tubes because they were held at improper storage temperatures. The affected units were distributed in Louisiana, Oklahoma, and Texas.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, but the source text does not report any illnesses, injuries, or hospitalizations. The hazard is a storage temperature deviation, which fits the criteria for a moderate severity recall involving low-risk contamination or voluntary precautionary measures without reported harm.
Plain-English summary
Fresenius Medical Care Holdings, Inc. is recalling 3 boxes of BD Vacutainer Serum Tubes (Red Top Plain Tube 6.0 ML), Part Number BD 367815, FMC Part Number 87-7815-4. These single-use tubes are used to collect, separate, transport, or process blood specimens for laboratory determinations for in vitro diagnostic use.
The recall was initiated because the products were held at improper storage temperature. The affected lot number is 3319877. The products were distributed in the states of Louisiana, Oklahoma, and Texas.
Consumers and healthcare facilities should stop using the affected tubes and contact the recalling firm for further instructions.
The recalled product
- 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.
- Manufacturer
- Fresenius Medical Care Holdings, Inc.
- Hazard
- Affected units
- 3
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot::3319877
Distribution
Part of a larger recall action
This product is one of 6 recalled by Fresenius Medical Care Holdings, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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