Fresenius Recalls BD Vacutainer SST Tubes for Improper Storage Temperature
Fresenius Medical Care is recalling 9 boxes of BD Vacutainer SST Tubes held at improper storage temperatures. The tubes 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 is a quality control issue without confirmed harm, fitting the criteria for a moderate severity score.
Plain-English summary
Fresenius Medical Care Holdings, Inc. is recalling 9 boxes of BD Vacutainer SST Tubes (Red/Grey Top, 3.5ml), Part Numbers BD 367981 and 87-7981-5. These single-use tubes are used to collect, separate, transport, or process blood specimens for laboratory determinations for in vitro diagnostic use, specifically for serum determination in chemistry.
The recall was initiated because the products were held at improper storage temperatures. The affected lots are 3305588 and 4006903. The products were distributed in the states of Louisiana, Oklahoma, and Texas.
Consumers and healthcare facilities should stop using these specific tubes and contact the recalling firm for further instructions or replacement.
The recalled product
- Product
- BD Vacutainer SST Tubes (RED/GREY TOP SST TUBE 3.5ML) Part Number: BD 367981 Part Number: 87-7981-5 Single use tube used to collect, separate, transport or process blood specimens for laboratory determinations for in vitro diagnostic use. serum determination in chemistry.
- Manufacturer
- Fresenius Medical Care Holdings, Inc.
- Hazard
- Affected units
- 9
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(s): 3305588 and 4006903
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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