Official recall record
Maquet Hemoconcentrator Set
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-01-18
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
The component "hemoconcentrator" was assembled into the finished product (hemoconcentrator tubing set) after its shelf-life had expired. After internal testing, it was determined that only one component lot was affected. Therefore, this field action is limited to products that containing hemoconcentrator of the one affected batch. Recall start date: December 29, 2023
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
ProductGuru Recalls republishes official safety information with attribution. We are not
the issuing authority and this page is not advice. If this product is a medical device or
medication, speak to a doctor or pharmacist. Found an error?
Report it — corrections are published.