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ANSM Safety Recall: Quadripod Cane 548 bis HMS-Vilgo

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Detected March 23rd, 2026
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Summary

The French National Agency for Medicines and Health Products Safety (ANSM) has announced a safety recall (R2608257) for the Quadripod cane model 548 bis HMS-Vilgo, initiated by the manufacturer HMS-Vilgo. The recall is directed at pharmacies, healthcare facilities, and home health providers.

What changed

The ANSM has been informed of a product recall action (R2608257) implemented by HMS-Vilgo for their Quadripod cane, model 548 bis. This action targets pharmacies, healthcare facilities, and home health providers. Users concerned have received a direct communication from the manufacturer.

This is a safety recall, indicating a potential risk associated with the product. Regulated entities that may have distributed or dispensed this product should cease its use and follow the manufacturer's instructions. For specific questions, direct inquiries to HMS-Vilgo. The recall notice includes a link to the manufacturer's letter dated March 23, 2026.

What to do next

  1. Cease distribution and use of the recalled Quadripod cane 548 bis HMS-Vilgo.
  2. Follow instructions provided by the manufacturer HMS-Vilgo.
  3. Address any inquiries directly to HMS-Vilgo.

Source document (simplified)

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Rappel n° R2608257 destiné aux pharmacies d'usage intérieur, officines, structures de soins de ville, grandes et moyennes surfaces et prestataires de santé à domicile L'ANSM a été informée de la mise en œuvre d’une action de retrait de produits effectuée par la société HMS-Vilgo.

Les utilisateurs concernés ont reçu le courrier ci-joint.

Cette action de sécurité est enregistrée à l’ANSM sous le n° R2608257. Pour toute question, merci de vous adresser directement à l’émetteur de l’action de sécurité. Téléchargez le courrier de la société HMS-Vilgo (23/03/2026)

Source

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

Classification

Agency
ANSM
Instrument
Enforcement
Legal weight
Binding
Stage
Final
Change scope
Substantive
Document ID
R2608257

Who this affects

Applies to
Healthcare providers Medical device makers
Industry sector
3345 Medical Device Manufacturing
Activity scope
Product Recalls
Geographic scope
France FR

Taxonomy

Primary area
Product Safety
Operational domain
Compliance
Topics
Medical Devices

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