The Recall Desk
ModerateFDA (Devices)·Z-2259-2018·Announced 2018-06-27

BD Vacutainer Plus Plastic Citrate Blood Collection Tubes Recalled for Overfill

Becton Dickinson is recalling BD Vacutainer Plus Plastic Citrate Blood Collection Tubes because approximately 3.4% of units exhibit overfill draw volumes.

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, which typically corresponds to a moderate severity score when no specific injuries or illnesses are reported in the source text.

Plain-English summary

Becton Dickinson & Company is recalling BD Vacutainer Plus Plastic Citrate Blood Collection Tubes (2.7mL, light blue top). The recall affects all lots of the product, which is an evacuated blood collection tube used to collect, transport, and process blood in a closed tube. The buffered sodium citrate additive provides an anticoagulated specimen for clinical laboratory coagulation assays.

The recall is issued because approximately 3.4% of these tubes will exhibit overfill draw volumes ranging from approximately 11% to 14%. The product was distributed to all 50 U.S. states, Puerto Rico, and various international locations from June 2, 2017, to the present.

The recalled product

Product
The BD Vacutainer Plus Plastic Citrate Blood Collection Tube is an evacuated blood collection tube that provides a means of collecting, transporting, and processing blood in a closed tube. The buffered sodium citrate additive provides an anticoagulated specimen that may be used f
Hazard

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)

  • All lots

Distribution

Distribution scope not specified by the agency.

Part of a larger recall action

This product is one of 3 recalled by Becton Dickinson & Company 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.

See all 3 products in this recall →