Changeflow GovPing Pharma & Drug Safety Product Recall: Klassiker Crutches and Rubber Tips
Urgent Enforcement Removed Final

Product Recall: Klassiker Crutches and Rubber Tips

Favicon for ansm.sante.fr ANSM Drug & Device Safety Alerts
Filed March 26th, 2026
Detected March 26th, 2026
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Summary

The ANSM has been informed of a product recall for Klassiker crutches and rubber tips, initiated by Ossenberg GmbH. This safety action, registered under number R2603198, affects pharmacies, community care facilities, large and medium-sized stores, and home healthcare providers. Affected users have been notified directly by the manufacturer.

What changed

The French National Agency for Medicines and Health Products Safety (ANSM) has announced a product recall for Klassiker crutches and rubber tips, identified by safety action number R2603198. The recall was initiated by the manufacturer, Ossenberg GmbH, due to safety concerns. This action specifically targets pharmacies, community care facilities, large and medium-sized stores, and home healthcare providers.

Compliance officers should note that this is a product recall, indicating a potential safety risk. Affected entities must ensure they have removed the specified products from their inventory and have followed the manufacturer's instructions for handling the recall. The ANSM directs any questions to the issuer of the safety action, Ossenberg GmbH, and provides a link to the manufacturer's notification letter dated March 26, 2026.

What to do next

  1. Ensure Klassiker crutches and rubber tips are removed from inventory.
  2. Follow manufacturer's instructions for handling the recall.

Source document (simplified)

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Rappel n° R2603198 destiné aux officines, structures de soins de ville, grandes et moyennes surfaces, prestataires de santé à domicile L'ANSM a été informée de la mise en œuvre d’une action de retrait de lot effectuée par la société Ossenberg GmbH.
Les utilisateurs concernés ont reçu le courrier ci-joint.

Cette action de sécurité est enregistrée à l’ANSM sous le n° R2603198.
Pour toute question, merci de vous adresser directement à l’émetteur de l’action de sécurité. Consultez le courrier de la société Ossenberg GmbH (26/03/2026)

Source

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

Classification

Agency
ANSM
Filed
March 26th, 2026
Instrument
Enforcement
Legal weight
Binding
Stage
Final
Change scope
Substantive
Document ID
R2603198

Who this affects

Applies to
Healthcare providers Retailers
Industry sector
3345 Medical Device Manufacturing
Activity scope
Product Recall
Geographic scope
France FR

Taxonomy

Primary area
Product Safety
Operational domain
Compliance
Topics
Medical Devices Consumer Protection

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