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[Recalled] Heavy Flow Bundle; Model Number: FG-BNDL-PC-REFHF; — Product lacks 510(k) clearance | FDA 2025-02-17
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Heavy Flow Bundle; Model Number: FG-BNDL-PC-REFHF; |
|---|---|
| Brand / manufacturer | DAYE (ANNE'S DAY LTD) |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0389-2026 |
| Country of notice | United Kingdom |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 17 February 2025 |
| EAN / barcode | 5060994741599 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Product lacks 510(k) clearance.
This Class II recall concerns device products distributed in United Kingdom and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from DAYE (ANNE'S DAY LTD)
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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