Arjo Tenor Mobile Lift Recall
Summary
Health Canada has issued a Type II recall for the Arjo Tenor Mobile Lift due to a brake defect that can cause uncontrolled descent. All affected units must be removed from service immediately until repaired by authorized personnel.
What changed
Health Canada has issued a Type II recall for the Arjo Tenor Mobile Lift, affecting all lots with model numbers KHA1000-US, TEN.107, and KHA1010-US. The recall is due to a supplier-related brake component defect in the lift actuator, which can lead to a loss of self-locking capability and sudden uncontrolled descent under load.
Healthcare providers must immediately remove all affected units from service and keep them out of operation until the actuator is replaced by authorized Arjo service personnel. This action is critical to prevent potential patient injury from uncontrolled descent. No specific deadline for replacement is provided, but the immediate removal from use is mandated.
What to do next
- Remove all affected Arjo Tenor Mobile Lifts from service immediately.
- Contact the manufacturer for actuator replacement by authorized personnel.
Source document (simplified)
Health product recall
Arjo Tenor Mobile Lift (French translation pending)
Brand(s)
Last updated
2026-03-13
Summary
Product Arjo Tenor Mobile Lift Issue Medical devices - Performance What to do Contact the manufacturer if you require additional information.
Audience Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
| --- | --- | --- |
| Arjo Tenor Mobile Lift | All lots. | KHA1000-US |
| Arjo Tenor Mobile Lift | All lots. | TEN.107 |
| Arjo Tenor Mobile Lift | All lots. | KHA1010-US |
Issue
A supplier‑related brake component defect in the Tenor lift actuator may cause loss of self‑locking and sudden uncontrolled descent under load. All affected units must be removed from use immediately and remain out of service until actuator replacement is completed by authorized Arjo service personnel.
Additional information
Details
Original published date:
2026-03-13
Alert / recall type Health product recall Category Health products - Medical devices - General hospital and personal use Companies Arjohuntleigh Ab
Hans Michelsensgatan 10, Malmo, Sweden, 21120
Published by Health Canada Audience Healthcare Recall class Type II Recall date
2026-03-02
Identification number RA-81735
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