FDA Device recall Z-2112-2012
Beekley Altus Floral Skin Markers -Order Number: 754 Product Usage: designed for Digital Mammography-Disposable skin markers for marking ar…
- FDA Device
- Class II
- terminated
- Published 2012-08-08
On 2012-08-08 the FDA classified a Class II recall of Beekley Altus Floral Skin Markers -Order Number: 754 Product Usage: designed for Digital Mammography-Disposable skin markers for marking ar… by Beekley, citing digital Skin Mammography Marker separating from the backing of the spot material.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2112-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-07-09 |
| Published | 2012-08-08 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Beekley |
| Distribution | US |
Product
Beekley Altus Floral Skin Markers -Order Number: 754 Product Usage: designed for Digital Mammography-Disposable skin markers for marking areas of concern or pain
Reason
Digital Skin Mammography Marker separating from the backing of the spot material
Identifiers
| code_info | Lot Numbers: A004 |
|---|
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-2112-2012%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.