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 Ultra Space. They come from safety-gate (1).
The published dates in this group run from 2026-05-08 to 2026-05-08. 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 pressure vessel could rupture due to design flaws and cause injuries to the users. The product does not comply with the requirements of the Transportable Pressure Equipment Directive.
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: 16/04/2026Type of economic operator to whom the measure(s) were ordered: ManufacturerCategory of measure(s): Ban on the marketing of the product and any accompanying measuresDate of entry into force: 16/04/2026Type 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: 16/04/2026