Public recall detail

Arjo Tenor Mobile Lift

2026-03-13

medium
General hospital and personal use Performance
Quick summary

Quick summary: Arjo Tenor Mobile Lift. Reason: Performance. Category: General hospital and personal use. Date: 2026-03-13.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Arjo Tenor Mobile Lift. Reason: Performance. Category: General hospital and personal use. Date: 2026-03-13.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandArjohuntleigh Ab
ProductArjo Tenor Mobile Lift
IssueMedical devices - Performance
Recall classType II
IdentificationRA-81735

Affected products

ProductArjo Tenor Mobile Lift
LotMore than 10 numbers, contact manufacturer.
ModelKHA1000-US
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionArjo Tenor Mobile Lift
ProductArjo Tenor Mobile Lift
LotMore than 10 numbers, contact manufacturer.
ModelTEN.107
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionArjo Tenor Mobile Lift
ProductArjo Tenor Mobile Lift
LotMore than 10 numbers, contact manufacturer.
ModelKHA1010-US
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionArjo Tenor Mobile Lift

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.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - General hospital and personal use
CompaniesArjohuntleigh Ab Hans Michelsensgatan 10, Malmo, Sweden, 21120
Recall date2026-03-02
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-81735
Background{}
CompaniesArjohuntleigh Ab Hans Michelsensgatan 10, Malmo, Sweden, 21120
AudiencesHealthcare
Source updated2026-03-19

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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