[Recalled] Beekley Altus Floral Skin Markers -Order Number: 754 Product Usage: designed for Digital Mammography-Disposable skin markers for marking areas of concern or pain — Digital Skin Mammography Marker separating from the backing
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Beekley Altus Floral Skin Markers -Order Number: 754 Product Usage: designed for Digital Mammography-Disposable skin markers for marking areas of concern or pain |
|---|---|
| Brand / manufacturer | Beekley Corporation |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2112-2012 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 09 July 2012 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Digital Skin Mammography Marker separating from the backing of the spot material
This Class II recall concerns device products distributed in United States 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 Beekley Corporation
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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