Lifedop 150/250/350 System - Probes (2017-10-06)
LifeDop 150/250/350 System Probes Recall LifeDop ultrasound probes (model 150/250/350) are being recalled across Canada due to a medical device issue. The recall is classified as Class I, which means the product could cause serious harm or death. The probes were distributed throughout Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2017-10-27
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/95a0b7aa-8f1a-4b53-add2-71d8e6fafb22