Vizishot 2 Flex
ViziShot 2 Flex Recall Summary ViziShot 2 Flex is being recalled across Canada due to labelling and packaging issues that affect the product's performance. This is a Class I recall, the most serious classification. The recall applies to all ViziShot 2 Flex products distributed in Canada.
- Product
- ViziShot 2 Flex
- Reason
- Labelling and packaging - Performance
- Classification
- Class II
- Category
- medical device recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2026-02-04
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/d84ef78e-6948-4548-9992-575ed015cca0