Results are official records from named sources. Coverage is incomplete. This site is not medical advice and does not publish drug labels, openFDA, Prop 65 or NIH DSLD records.
No Wikidata QID is asserted for this brand in the current slice.
What the governed recall projection contains
This page groups 1 official recall action that explicitly name Inter-Tech. They come from safety-gate (1).
The published dates in this group run from 2026-02-06 to 2026-02-06. The projection was retrieved 2026-09-04T21:09:13.297Z; dates describe the notices, not whether every affected unit has been repaired.
1 distinct published hazard statement is represented. Open each action for its hazard, remedy, jurisdiction, native identifier and official source link. Similar brand names are not merged unless the source record names the brand.
The creepage distance between the live primary parts and accessible DC output connectors is not adequate. The user could touch live parts (such as the connector of the power supply DC output) and receive an electric shock. The product does not comply with the requirements of the Low Voltage Directive, nor with the European standard EN 62368-1.
Published remedy: Type of economic operator taking notified measure(s): DistributorCategory of measure(s): Recall of the product from end usersDate of entry into force: 26/01/2026