Product Wiki · Recalls · EU Safety Gate (RAPEX)

Hermetic Dry Bag - Medi size — recall SR/02966/26

EU Safety Gate (RAPEX) · United Kingdom in respect of Northern Ireland · 2026-10-23 · Serious risk

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked on this page. No AI-generated text appears on this page. How we use AI →
Agency
EU Safety Gate (RAPEX)
Recall identifier
SR/02966/26
Date of alert
2026-10-23
Country / jurisdiction
United Kingdom in respect of Northern Ireland
Risk level
Serious risk
Risk type
Choking, Injuries
Brand
Fidlock
Product category
Hobby/sports equipment
Product type
Dry bag
Barcode (EAN/GTIN)
4251207401183
🔴 Serious hazard — Reported risk: 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

Check whether your product matches this notice (name, batch, dates). If it does, stop using it and follow the instructions in the official notice — refund, return, repair or disposal are set by the issuing authority and the business, and they differ per recall. Official notice from EU Safety Gate (RAPEX) →

Action taken by the authority
Type of economic operator taking notified measure
Manufacturer
Category of measure
Recall of the product from end users
Date of entry into force
03/09/2026
Primary source: https://ec.europa.eu/safety-gate-alerts/screen/webReport/alertDetail/10119224

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.