Hybrid Hydrophilic Microguidewire
Hybrid Hydrophilic Microguidewire Recall A medical device called the Hybrid Hydrophilic Microguidewire is being recalled across Canada due to a device performance issue. This guidewire is used in medical procedures to help navigate through blood vessels or other pathways in the body. The recall is classified as Class II, which indicates a potential health risk.
- Product
- Hybrid Hydrophilic Microguidewire
- Reason
- Device performance issue
- Classification
- Class II
- Category
- medical device recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2026-07-03
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/08c330a3-6c88-4e3d-af03-0efe1b4a6c31