4 Ml K2 Edta Tube (2016-07-27)

Recall Summary A 4 mL K2 EDTA tube (a blood collection container) was recalled across Canada starting July 27, 2016, due to issues classified as a Class I medical device concern. K2 EDTA tubes are used in healthcare settings to collect blood samples for testing.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-08-19

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/87c99d34-af30-4173-8c49-4b6f222e2216