Bd Vacutainer Sodium Fluoride Tube (2019-06-14)
BD Vacutainer Sodium Fluoride Tube Recall BD Vacutainer Sodium Fluoride tubes used for blood collection are being recalled across Canada because they do not meet quality standards for medical devices. The recall affects tubes distributed throughout Canada. This is a Class I recall, which is the most serious classification.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-08-30
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/68285660-4f5d-4f1c-8972-07a3c5c8c44e