Beekley Medical 0-SPOT Mammography Skin Markers REF 652 — Class III medical device recall Z-2309-2017
Terminated recall by Beekley Corporation, reported 2017-06-14, distributed in AR, CA, GA, IL, MN, NV, NY, TX…. Mammography Skin Marker 0 -SPOT (REF 652) product was mis-labeled with A-SPOT (REF 651) labels
| Recall number | Z-2309-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beekley Corporation, Bristol, CT, United States |
| Recall initiated | 2017-05-08 |
| Classified | 2017-06-07 |
| Reported by FDA | 2017-06-14 |
| Terminated | 2017-06-20 |
| Distributed | AR, CA, GA, IL, MN, NV, NY, TX, WI |
| Countries outside the US | CA |
| Reason classes | labeling |
| Lot numbers | 652.04251701 |
| Model numbers | 652 |
Product
Beekley Medical 0-SPOT Mammography Skin Markers REF 652
Reason for recall
Mammography Skin Marker 0 -SPOT (REF 652) product was mis-labeled with A-SPOT (REF 651) labels
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2309-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.