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Product Recall: Fidlock Hermetic Dry Bag (2609-0075)
Official product safety report including images and corrective action →
⚠ What You Should Do
The product has been recalled from end users by Fidlock GmbH.
Consumers should cease use of the product immediately, keep it out of reach of children, and dispose of it safely. Contact Fidlock directly via recall_2609@fidlock.com to register for a refund or replacement.
For more information, please visit Recall: HERMETIC dry bag medi.
Recall Details
Hazard
Products from lot number 2409140930201 have a manufacturing defect affecting 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 and present a risk of injuries if swallowed, especially by young children. If one or more magnets are swallowed, they can attract each other within the body, causing serious internal injuries.
The product does not meet the requirements of the General Product Safety Regulations 2005.
Corrective Action
The product has been recalled from end users by Fidlock GmbH.
Consumers should cease use of the product immediately, keep it out of reach of children, and dispose of it safely. Contact Fidlock directly via recall_2609@fidlock.com to register for a refund or replacement.
For more information, please visit Recall: HERMETIC dry bag medi.
Why This Product Is Dangerous
Products from lot number 2409140930201 have a manufacturing defect affecting 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 and present a risk of injuries if swallowed, especially by young children. If one or more magnets are swallowed, they can attract each other within the body, causing serious internal injuries.
The product does not meet the requirements of the General Product Safety Regulations 2005.