FDA Device recall Z-2309-2017
Beekley Medical 0-SPOT Mammography Skin Markers REF 652
- FDA Device
- Class III
- terminated
- Published 2017-06-14
On 2017-06-14 the FDA classified a Class III recall of Beekley Medical 0-SPOT Mammography Skin Markers REF 652 by Beekley, citing mammography Skin Marker 0 -SPOT (REF 652) product was mis-labeled with A-SPOT (REF 651) labels.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2309-2017 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2017-05-08 |
| Published | 2017-06-14 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Beekley |
| Distribution | AR, CA, GA, IL, MN, NV, NY, TX, WI |
Product
Beekley Medical 0-SPOT Mammography Skin Markers REF 652
Reason
Mammography Skin Marker 0 -SPOT (REF 652) product was mis-labeled with A-SPOT (REF 651) labels
Identifiers
| code_info | LOT 652.04251701 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2309-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.