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Fresenius Dali 750 Kit Hemadsorption Device Safety Notice

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Published April 7th, 2026
Detected April 7th, 2026
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Summary

ANSM issued a safety alert regarding a field safety corrective action conducted by Fresenius Medical Care AG for the Dali 750 Kit hemadsorption device. The safety action is registered under reference R2608923. Users of this medical device have received direct correspondence from Fresenius with details of the corrective measure.

What changed

ANSM published a medical device safety notice informing healthcare facilities and professionals of a safety action taken by Fresenius Medical Care AG concerning the Dali 750 Kit hemadsorption system. The corrective action bears ANSM registration number R2608923, with the manufacturer's detailed letter dated 07/04/2026.

Healthcare providers and medical device users should download the Fresenius correspondence letter from the ANSM website to determine whether their facility is affected by this action. Facilities using the Dali 750 Kit should review the safety information and follow any instructions provided by Fresenius Medical Care AG directly, as ANSM has directed all inquiries to the manufacturer.

What to do next

  1. Download and review the Fresenius Medical Care AG safety letter (PDF dated 07/04/2026)
  2. Identify whether your facility uses or stocks the Dali 750 Kit hemadsorption device
  3. Contact Fresenius Medical Care AG directly for questions and follow any device handling instructions provided

Source document (simplified)

A+ A-

Information n° R2608923 destinée aux pharmacies d'usage intérieur, laboratoires d'analyses de biologie médicale, officines et structures de soins de ville L'ANSM a été informée de la mise en œuvre d’une action de sécurité effectué par la société Fresenius Medical Care AG.

Les utilisateurs concernés ont reçu le courrier ci-joint.

Cette action de sécurité est enregistrée à l’ANSM sous le n° R2608923. Pour toute question, merci de vous adresser directement à l’émetteur de l’action de sécurité. Téléchargez le courrier de la société Fresenius Medical Care AG (07/04/2026)

Source

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

Classification

Agency
ANSM
Published
April 7th, 2026
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
R2608923

Who this affects

Applies to
Healthcare providers Medical device makers
Industry sector
3345 Medical Device Manufacturing 6211 Healthcare Providers
Activity scope
Medical Device Safety Monitoring
Geographic scope
France FR

Taxonomy

Primary area
Healthcare
Operational domain
Compliance
Topics
Medical Devices Public Health

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