Hollow Fiber Hemodialyzers
Hollow Fiber Hemodialyzers used in kidney dialysis treatment are being recalled across Canada due to labelling and packaging errors. The recall affects all Canadian users of this medical device. The FDA classified this as a Class I recall, indicating a serious issue with how the product is labeled and packaged.
- Product
- Hollow Fiber Hemodialyzers
- Reason
- Labelling and packaging
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2025-09-16
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/28411137-b462-4a30-ae0b-a1689d9454af