Quality & complianceOfficial

Greek regulator EOF announces recall of lots of neurosurgical plate and fast flap kit devices

🇬🇷 EOF · Wed 21 Oct 2026

EOF has published a decision recalling specific lots of NEUROPACK straight plates and a sterile fast flap kit with a large bur hole, but the notice excerpt gives no reason or lot numbers.

The Greek National Organisation for Medicines (EOF) has announced the recall of lots of two medical device products: NEUROPACK, 1 LONG & 2 MED STRAIGHT PLATES, and STERILE FAST FLAP KIT, LARGE BUR HOLE, 1P. The notice is registered under protocol number 124462 and is dated 21 October 2026.

The text available is only a short listing that points readers to the full decision on the EOF website. It does not say why the lots are being recalled, which lot numbers are affected, who manufactured the devices or what action users are asked to take.

As general context, a recall of medical device lots usually means affected units must be identified and quarantined, and returned or otherwise dealt with according to instructions from the manufacturer or the competent authority. Those details have to be taken from the full notice, not from this summary.

What it means for your team

  • Quality and regulatory teams in Greece should read the full EOF decision (protocol no. 124462) to find the affected lots, the reason and the required actions.
  • Distributors, hospitals and importers holding NEUROPACK plates or the fast flap kit should check their inventory against the lot list once they have it.
  • Until the reason for the recall is confirmed from the full notice, it should not be assumed to be a safety, quality or labelling problem.

Official source: EOF ↗

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

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