Beekley Altus Floral Skin Markers -Order Number: 754 Product Usage:… — Class II medical device recall Z-2112-2012
Terminated recall by Beekley Corporation, reported 2012-08-08, distributed nationwide. Digital Skin Mammography Marker separating from the backing of the spot material
| Recall number | Z-2112-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beekley Corporation, Bristol, CT, United States |
| Recall initiated | 2012-07-09 |
| Classified | 2012-07-30 |
| Reported by FDA | 2012-08-08 |
| Terminated | 2013-07-09 |
| Distributed | Nationwide (US) |
| Quantity | 6,420 units |
| Lot numbers | A004 |
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 for recall
Digital Skin Mammography Marker separating from the backing of the spot material
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-2112-2012. 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.