Beekley Corporation
5 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (5)
Registered facilities (1)
- Beekley Corporation FEI 3000204334 · CT
Recalls & enforcement
- Class IITerminated2018-06-13There is a potential for imaging artifact to mimic calcifications on patient's mammograms
- Class IIITerminated2017-05-08Mammography Skin Marker 0 -SPOT (REF 652) product was mis-labeled with A-SPOT (REF 651) labels
- Class IIITerminated2013-06-19Light Image O-Spots Dispenser mislabeled as Soft n' Stretchy Light Image S-Spots
- Class IITerminated2012-07-09Digital Skin Mammography Marker separating from the backing of the spot material
- Class IITerminated2012-07-02Imaging artifact can occur on mammogram result
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “Beekley Corporation — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-10023165-beekley-corporation/
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