Maquet Percutaneous Insertion Kit And Dilator Sets
Recall Summary Maquet Percutaneous Insertion Kits and Dilator Sets are being recalled in Canada due to sterility concerns. These are medical devices used for percutaneous procedures. The recall is classified as Class II and affects products distributed across Canada.
- Product
- Maquet Percutaneous Insertion Kit and Dilator Sets
- Reason
- Sterility concern
- Classification
- Class II
- Category
- medical device recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2026-08-26
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/00e64958-92b9-44ba-9cb5-e14de9f9fde4