Official recall record
Q-LINK 13 components and LikoScale™ Adapter Kits
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-06-03
- Country of alert
- Canada
- Alert level
- Type I
- Alert type
- recall
What the authority reported
Baxter Corporation is issuing an urgent medical device recall for the Q-LINK 13 lift component due to customer reports related to the improper attachment of the Q-LINK 13 (false latching) with the quick-release hook. The LikoScale™ Adapter Kit contains the Q-LINK 13 component and shares the potential for improper attachment. Recall start date: May 29, 2025
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.
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