Bd Vacutainer K2 Edta (k2e) 3.6mg Blood Collection Tubes (2017-08-28)

BD Vacutainer K2 EDTA Blood Collection Tubes Recall BD Vacutainer K2 EDTA 3.6mg blood collection tubes are being recalled across Canada due to a medical device issue. These tubes are used by healthcare providers to collect blood samples for testing. The recall affects all tubes of this type that were distributed in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-09-26

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/d558890a-074b-409b-ad6a-f7cf49af400e