Class III — Beekley Corporation
| Recalling firm | Beekley Corporation |
|---|---|
| Registered facility | Beekley Corporation (the firm's only registered facility) |
| Classification | Class III |
| Status | Terminated |
| Reason | Light Image O-Spots Dispenser mislabeled as Soft n' Stretchy Light Image S-Spots |
| Product | Beekley Spots Light Image O-Spots for Mammography Catalog Number: 252 Product Usage: To identify raised moles in Mammography |
| Quantity | 81 boxes |
| Distribution | Worldwide Distribution - USA in the states of CA, FL, MA, NC, NY, and PA. |
| Initiated | 2013-06-19 |
| Classified | 2014-06-12 |
| Terminated | 2014-06-16 |
| Recall number | Z-1787-2014 |
| 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-1787-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/65483/
Alerts for Beekley Corporation
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.