Changeflow GovPing Drug Safety ArjoHuntleigh Tenor Mobile Hoist Safety Alert
Priority review Notice Removed Final

ArjoHuntleigh Tenor Mobile Hoist Safety Alert

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Detected March 13th, 2026
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Summary

The French National Agency for the Safety of Medicines and Health Products (ANSM) has announced a product recall for the ArjoHuntleigh Tenor mobile hoist. This action, registered under number R2606757, is being implemented by the manufacturer ArjoHuntleigh AB.

What changed

The ANSM has been informed of a product recall action for the ArjoHuntleigh Tenor mobile hoist, designated under safety action number R2606757. This notice is directed towards pharmacies, healthcare facilities, and home healthcare providers. The specific details and instructions for users are provided in a letter from ArjoHuntleigh AB, dated March 13, 2026.

Healthcare providers and facilities using the ArjoHuntleigh Tenor mobile hoist should consult the provided letter from the manufacturer for specific instructions regarding this recall. Any questions should be directed to ArjoHuntleigh AB. This action indicates a potential safety issue with the device, and compliance with the manufacturer's instructions is critical to ensure patient safety and regulatory adherence.

What to do next

  1. Review ArjoHuntleigh AB's recall letter dated 2026-03-13.
  2. Follow manufacturer instructions for the ArjoHuntleigh Tenor mobile hoist.
  3. Direct any questions regarding the recall to ArjoHuntleigh AB.

Source document (simplified)

A+ A-

Information n° R2606757 destinée aux pharmacies d'usage intérieur, structures de soins de ville, prestataires de santé à domicile L'ANSM a été informée de la mise en œuvre d’une action de retrait de produit effectuée par la société ArjoHuntleigh AB.
Les utilisateurs concernés ont reçu le courrier ci-joint.

Cette action de sécurité est enregistrée à l’ANSM sous le n° R2606757.
Pour toute question, merci de vous adresser directement à l’émetteur de l’action de sécurité. Consultez le courrier de la société ArjoHuntleigh AB (13/03/2026)

Source

Analysis generated by AI. Source diff and links are from the original.

Classification

Agency
Various
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Substantive

Who this affects

Applies to
Healthcare providers
Geographic scope
National (France)

Taxonomy

Primary area
Healthcare
Operational domain
Compliance
Topics
Product Safety Medical Devices

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