Carestation 620 And 650 (2017-05-02)
Carestation 620 and 650 Recall Summary Carestation 620 and 650 anesthesia delivery systems were recalled across Canada due to a medical device issue. The FDA classified this as a Class I recall, indicating a serious problem with the equipment. The recall affects these anesthesia machines that were distributed throughout Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2017-06-12
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/39c5f667-50a1-46d6-9864-1420e6393f81