Class II — Beekley Corporation
| Recalling firm | Beekley Corporation |
|---|---|
| Registered facility | Beekley Corporation (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Digital Skin Mammography Marker separating from the backing of the spot material |
| 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 |
| Quantity | 6420 units |
| Distribution | US Nationwide Distribution |
| Initiated | 2012-07-09 |
| Classified | 2012-07-30 |
| Terminated | 2013-07-09 |
| Recall number | Z-2112-2012 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Beekley Corporation (Z-2112-2012).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/62526/
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