Class III — Beekley Corporation
| Recalling firm | Beekley Corporation |
|---|---|
| Registered facility | Beekley Corporation (the firm's only registered facility) |
| Classification | Class III |
| Status | Terminated |
| Reason | Mammography Skin Marker 0 -SPOT (REF 652) product was mis-labeled with A-SPOT (REF 651) labels |
| Product | Beekley Medical 0-SPOT Mammography Skin Markers REF 652 |
| Quantity | 104 boxes (58/box)= 6,032 total units |
| Distribution | US Distribution to the states of : AR, CA GA, IL, TX, MN, NV, NY, WI., and Internationally to Canada. |
| Initiated | 2017-05-08 |
| Classified | 2017-06-07 |
| Terminated | 2017-06-20 |
| Recall number | Z-2309-2017 |
| 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 III recall — Beekley Corporation (Z-2309-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/77295/
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