FDA Device recall Z-1787-2014
Beekley Spots Light Image O-Spots for Mammography Catalog Number: 252 Product Usage: To identify raised moles in Mammography
- FDA Device
- Class III
- terminated
- Published 2014-06-18
On 2014-06-18 the FDA classified a Class III recall of Beekley Spots Light Image O-Spots for Mammography Catalog Number: 252 Product Usage: To identify raised moles in Mammography by Beekley, citing light Image O-Spots Dispenser mislabeled as Soft n' Stretchy Light Image S-Spots.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1787-2014 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-06-19 |
| Published | 2014-06-18 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Beekley |
| Distribution | CA, FL, MA, NC, NY, PA |
Product
Beekley Spots Light Image O-Spots for Mammography Catalog Number: 252 Product Usage: To identify raised moles in Mammography
Reason
Light Image O-Spots Dispenser mislabeled as Soft n' Stretchy Light Image S-Spots
Identifiers
| code_info | Lot Number: 252.04261301 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1787-2014%22
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