Changeflow GovPing Pharma & Drug Safety MarClamp Cut IQ Safety Notice - KLS Martin Group
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MarClamp Cut IQ Safety Notice - KLS Martin Group

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Summary

ANSM issued safety notice R2608256 regarding KLS Martin Group's MarClamp Cut IQ electrosurgical device with instrument coding 23cm. Hospital pharmacies and healthcare establishments are directed to review and act upon the attached manufacturer safety communication. This is a Class I medical device safety action.

Published by ANSM on ansm.sante.fr . Detected, standardized, and enriched by GovPing. Review our methodology and editorial standards .

What changed

KLS Martin Group initiated a safety action (R2608256) for the MarClamp Cut IQ electrosurgical device with instrument coding 23cm. ANSM notified hospital pharmacies and healthcare establishments that affected users have already received direct correspondence from the manufacturer. The safety action letter is dated March 31, 2026.

Healthcare facilities must review the attached KLS Martin Group letter, determine if their institution uses the MarClamp Cut IQ device, and implement any corrective measures specified by the manufacturer. Pharmacy and clinical staff should coordinate to ensure all affected equipment is identified and proper protocols are followed. Direct questions to the manufacturer as indicated in the notice.

What to do next

  1. Review the attached KLS Martin Group safety letter dated 31/03/2026
  2. Identify whether your facility uses the MarClamp Cut IQ electrosurgical device
  3. Implement any corrective measures specified in the manufacturer correspondence

Archived snapshot

Mar 31, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

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Information n° R2608256 destinée aux pharmacies d'usage intérieur, établissements de santé L'ANSM a été informée de la mise en œuvre d’une action de sécurité effectuée par la société KLS Martin Group.
Les utilisateurs concernés ont reçu le courrier ci-joint.

Cette action de sécurité est enregistrée à l’ANSM sous le n° R2608256.
Pour toute question, merci de vous adresser directement à l’émetteur de l’action de sécurité. Consultez le courrier de la société KLS Martin Group (31/03/2026)

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Last updated

Classification

Agency
ANSM
Published
March 31st, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Substantive
Document ID
R2608256
Docket
R2608256

Who this affects

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

Taxonomy

Primary area
Medical Devices
Operational domain
Clinical Operations
Topics
Healthcare Product Safety

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