Vacuette 4 Ml Fx Sodium Fluoride / Potassium Oxal (2016-04-26)
Recall Summary Vacuette 4 mL FX blood collection tubes containing sodium fluoride and potassium oxalate are being recalled across Canada. The recall was issued on April 26, 2016, and is classified as Class I, indicating a serious safety concern. This recall affects medical devices used for blood sample collection.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-05-31
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/9e9004e8-21aa-43eb-b545-c103af08615e