Olympus Gyrus ACMI Everest Cutting Forceps Lot Recall R2607996
Summary
ANSM registered safety action R2607996 concerning a lot withdrawal of Everest cutting forceps (pince coupante) manufactured by Olympus Gyrus ACMI. The recall was initiated by Olympus following notification to ANSM. Affected users received a direct communication from the manufacturer. This action targets hospital pharmacies and health establishments that hold the implicated lot.
What changed
ANSM recorded safety action R2607996 for a lot-level withdrawal of Olympus Gyrus ACMI Everest cutting forceps (pince coupante EverEST). The recall was initiated by the manufacturer Olympus and communicated directly to affected healthcare establishments and hospital pharmacies via a manufacturer letter dated 17 April 2026.
Healthcare establishments and hospital pharmacies that received the manufacturer's recall communication should review their inventory for the implicated lot and contact Olympus directly for instructions. As a medical device recall, affected parties should ensure compliance with applicable medical device reporting obligations if adverse events are identified.
What to do next
- Contact the manufacturer (Olympus) for further information regarding the recalled lot
Archived snapshot
Apr 17, 2026GovPing 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.
Rappel n° R2607996 destiné aux pharmacies d'usage intérieur et établissements de santé L'ANSM a été informée de la mise en œuvre d’un retrait de lot effectué par la société Olympus.
Les utilisateurs concernés ont reçu le courrier ci-joint.
Cette action de sécurité est enregistrée à l’ANSM sous le n° R2607996. Pour toute question, merci de vous adresser directement à l’émetteur de l’action de sécurité. Téléchargez le courrier de la société Olympus (17/04/2026)
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