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 3 official recall actions that explicitly name Bono Bijou. They come from safety-gate (3).
The published dates in this group run from 2026-01-30 to 2026-01-30. The projection was retrieved 2026-09-04T21:09:13.297Z; dates describe the notices, not whether every affected unit has been repaired.
3 distinct published hazard statements are 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 rate of nickel release is too high (measured value up to 20.6 µg/cm2/week). Nickel is a strong sensitiser and causes allergic reactions if present in articles that come into direct and prolonged contact with the skin. The product does not comply with the REACH Regulation nor with the General Product Safety Regulation.
Published remedy: Type of economic operator to whom the measure(s) were ordered: ImporterCategory of measure(s): Recall of the product from end usersDate of entry into force: Unknown
The rate of nickel release from the ring is too high (measured value up to 20.6 µg/cm2/week). Nickel is a strong sensitiser and causes allergic reactions if present in articles that come into direct and prolonged contact with the skin. The product does not comply with the General Product Safety Regulation nor the REACH Regulation.
Published remedy: Type of economic operator to whom the measure(s) were ordered: ImporterCategory of measure(s): Withdrawal of the product from the marketDate of entry into force: Unknown
The rate of nickel release is too high (measured value up to 20.6 µg/cm2/week). Nickel is a strong sensitiser and causes allergic reactions if present in articles that come into direct and prolonged contact with the skin. The product does not comply with the General Product Safety Regulation nor the REACH Regulation.
Published remedy: Type of economic operator to whom the measure(s) were ordered: ImporterCategory of measure(s): Withdrawal of the product from the marketDate of entry into force: Unknown