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 Skylotec. They come from safety-gate (1).
The published dates in this group run from 2026-05-01 to 2026-05-01. 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 total filtration capacity of the mask is insufficient (measured values as low as 79%). Consequently, the product does not fulfil the health and safety requirements. Thus, even if combined with other recommended measures, it may not properly protect. The product does not comply with the Personal Protective Equipment (PPE) Regulation nor with European standard EN 149.
Published remedy: Type of economic operator to whom the measure(s) were ordered: ManufacturerCategory of measure(s): Withdrawal of the product from the marketDate of entry into force: 06/11/2025Type of economic operator to whom the measure(s) were ordered: ManufacturerCategory of measure(s): Recall of the product from end usersDate of entry into force: 06/11/2025