Bd Microtrainer: Tubes With K2e (k2edta), Pst Tubes With Lh (lithium Heparin) - Amber, Pst Tube With Lh (lithium Heparin), Z (no Additive Tubes), Sst And Bd Microtrainer Sst - Amber, Tubes With Fe (

Recall Summary BD is recalling certain blood collection tubes sold in Canada because they do not meet required specifications for sterility, bacterial endotoxin levels, or proper labeling. The affected products include tubes with various additives (K2EDTA, Lithium Heparin, and others) used for blood draws in medical settings. This is a Class I recall, meaning there is a reasonable possibility that the tubes could cause serious adverse health effects.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-05-31

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/cc0ed072-cdc5-4dfc-9334-0deb5d48d909