Arjo Tenor Mobile Lift Recall
Summary
Health Canada has issued a Type II recall for the Arjo Tenor Mobile Lift due to a defect in the brake component of the actuator. The defect can cause a loss of self-locking and uncontrolled descent, posing a safety risk. Affected units must be removed from use immediately.
What changed
Health Canada has issued a Type II recall for the Arjo Tenor Mobile Lift, specifically models KHA1000-US, TEN.107, and KHA1010-US, affecting all lots. The recall is due to a supplier-related defect in the lift actuator's brake component, which can lead to a loss of self-locking capability and sudden, uncontrolled descent under load. This poses a significant safety risk to patients and users.
Healthcare providers and facilities in possession of the affected Arjo Tenor Mobile Lifts must immediately remove these units from service. The lifts should not be used until the actuator is replaced by authorized Arjo service personnel. Users are advised to contact the manufacturer for further information and to arrange for the necessary repairs. Failure to comply could result in patient injury.
What to do next
- Remove all affected Arjo Tenor Mobile Lifts from service immediately.
- Contact the manufacturer for actuator replacement by authorized personnel.
- Do not use affected units until repairs are completed.
Source document (simplified)
Health product recall
Arjo Tenor Mobile Lift
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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