Changeflow GovPing Pharma & Drug Safety Safety Notice Cryotubes Cryo.s Medical Devices ...
Priority review Enforcement Amended Final

Safety Notice Cryotubes Cryo.s Medical Devices by Greiner Bio-One

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Summary

ANSM recorded safety action R2609958 concerning Cryotubes Cryo.s medical devices manufactured by Greiner Bio-One. The company has issued a safety communication dated 17/04/2026 to affected users. ANSM directs users to contact Greiner Bio-One directly for details and questions regarding the action.

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

What changed

Greiner Bio-One initiated a safety action for Cryotubes Cryo.s medical devices, registered with ANSM under reference R2609958. ANSM has recorded this action and published a notice informing medical biology laboratories of the action and the attached company communication dated 17/04/2026.

Medical biology laboratories using Cryotubes Cryo.s devices should review the attached communication from Greiner Bio-One and follow any instructions provided. Users are directed to contact Greiner Bio-One directly for questions regarding the specific nature of the safety action and required steps.

What to do next

  1. Contact the issuer of the safety action for questions

Archived snapshot

Apr 17, 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.

Information n° R2609958 destinée aux laboratoires d'analyses de biologie médicale L'ANSM a été informée de la mise en œuvre d’une action de sécurité effectuée par la société Greiner Bio-One.

Les utilisateurs concernés ont reçu le courrier ci-joint.

Cette action de sécurité est enregistrée à l’ANSM sous le n° R2609958. Pour toute question, merci de vous adresser directement à l’émetteur de l’action de sécurité. Téléchargez le courrier de la société Greiner Bio-One (17/04/2026)

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Last updated

Classification

Agency
ANSM
Filed
April 17th, 2026
Instrument
Enforcement
Legal weight
Binding
Stage
Final
Change scope
Substantive
Document ID
R2609958
Docket
R2609958

Who this affects

Applies to
Healthcare providers
Industry sector
3345 Medical Device Manufacturing
Activity scope
Medical device safety action Product recall response
Geographic scope
France FR

Taxonomy

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

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