ProductGuru Recalls

Official recall record

Hermetic Dry Bag - Medi size

EU Safety Gate (RAPEX) · 2026-10-23 · United KingdomSerious risk
Issuing authority
EU Safety Gate (RAPEX)
Alert date
2026-10-23
Country of alert
United Kingdom
Alert level
Serious risk
Risk type (official)
Choking, Injuries
Barcode (EAN/GTIN)
4251207401183
Brand on record
Fidlock

What the authority reported

The adhesive bond between the closure strips and the bag film. As a result, the closure strips may detach partially or completely during use, causing the product to lose its intended function and potentially releasing the enclosed magnets. The magnets constitute small parts. A child can put them in the mouth and choke. Moreover, if a child swallows them, they could attract one another causing intestinal blockage or perforation. The product does not comply with the General Product Safety Regulation.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: EU Safety Gate (RAPEX) — official record →
Record last checked against the registry on 2026-11-07.

More recalls: EU Safety Gate (RAPEX) · United Kingdom · all filters

Same barcode in other registries

The same EAN appears in 2 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.

ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.