Quality & complianceOfficial

Greek regulator EOF announces batch recall of two TELIC S.A.U. medical devices

🇬🇷 EOF · Mon 26 Oct 2026

EOF has published a recall decision covering a batch of BLAYCO Electrode tip cleaner and DORMO-STRIP Vein strippers, both made by TELIC S.A.U.

Greece's national medicines organisation, EOF, has announced the recall of a batch of two medical devices supplied by TELIC S.A.U. The notice is filed under reference number 119698.

The first product is the BLAYCO Electrode tip cleaner, classified as MDD Class I. The second is the DORMO-STRIP Vein strippers, classified as MDD Class IIa. Both classifications fall under the Medical Devices Directive.

The text published by EOF is only a short notice. It does not name the affected batch numbers, give a reason for the recall or describe any corrective actions. It points readers to a separate decision document, which is linked from the page.

As general context, a batch recall under the Medical Devices Directive normally requires the manufacturer or its distributor to withdraw the identified lots from the supply chain and inform users. The scope and actions are set out in the competent authority's decision and any related field safety notice.

What it means for your team

  • Check the full EOF decision (ref. 119698) for the affected batch numbers, the recall rationale and the required actions.
  • Quality and regulatory teams with TELIC S.A.U. products on the Greek market should confirm whether any stock or customers are affected.
  • Vigilance teams should confirm whether the recall triggers internal complaint or incident reviews for these two devices.

Official source: EOF ↗

Article written by VigiEye from the official source (EOF). AI-assisted; check the source before acting.

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