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 Omtech. They come from safety-gate (1).
The published dates in this group run from 2026-03-13 to 2026-03-13. 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.
Because the safety mechanisms are easily bypassed, and because of the lack of a base plate, direct access to laser radiation during operation is possible. Looking directly into the laser beam or exposure via scattered radiation could damage a person’s sight. The product does not comply with the requirements of the Machinery Directive nor with the European standard EN 60825-1.
Published remedy: Type of economic operator taking notified measure(s): ManufacturerCategory of measure(s): Making the marketing of the product subject to prior conditionsDate of entry into force: 11/01/2026Type of economic operator taking notified measure(s): ManufacturerCategory of measure(s): Withdrawal of the product from the marketDate of entry into force: 11/01/2026Type of economic operator taking notified measure(s): ManufacturerCategory of measure(s): Marking the product with appropriate warnings on the risksDate of entry into force: 11/01/2026