Slovenia's JAZMP publishes October 2026 medical device field safety notices
The Slovenian agency has posted the month's safety corrective action notices received from manufacturers and authorised representatives, while warning that the list may be incomplete.
The Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (JAZMP) has made available on its website the field safety notices it received in October 2026. The notices relate to medical devices and come from manufacturers or their authorised representatives.
JAZMP describes a notice of this kind as a written communication from the manufacturer or authorised representative. It sets out the safety corrective actions needed to keep devices safe to use and to reduce the likelihood of events harmful to health.
According to the agency, the manufacturer or authorised representative must notify both JAZMP and the users of the devices in writing. The manufacturer must also ensure that all users are informed without delay.
JAZMP cautions that the monthly list may not be complete, since it only covers notices that the agency itself has received. Anyone who receives a field safety notice that does not appear on the list is asked to report it to JAZMP by email.
The source text does not detail individual products, manufacturers or the specific actions involved. Those details are in the notices themselves on the JAZMP website.
What it means for your team
- Vigilance and QA teams should review the October 2026 list for devices they place on the market, distribute or use in Slovenia, and check whether follow-up is needed.
- Manufacturers and authorised representatives should confirm that every field safety notice issued for Slovenia has reached JAZMP and all affected users without delay.
- Because the list may be incomplete, companies and users who hold a notice that is missing from it should tell JAZMP.
Article written by VigiEye from the official source (JAZMP). AI-assisted; check the source before acting.
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