Bd Vacutainer Tube Sodium Fluoride/potassium Oxalate
BD Vacutainer Tube Sodium Fluoride/Potassium Oxalate Recall BD Vacutainer Tubes containing Sodium Fluoride/Potassium Oxalate are being recalled across Canada because they are not performing as intended. These are blood collection tubes used in medical testing. This is a Class I recall, meaning there is a serious potential health risk.
- Product
- BD Vacutainer Tube Sodium Fluoride/Potassium Oxalate
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2022-09-28
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/1c5f0827-1735-47e2-80c7-3845dcd60c94