Recall Z-2112-2012— Beekley Corporation
Class II · Terminated
Class II FDA medical device recall by Beekley Corporation, initiated 2012-07-09, terminated 2013-07-09. FDA's recall record names no specific 510(k) clearance for this event. 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.
- Recalling firm
- Beekley Corporation
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2012-07-09
- Terminated
- 2013-07-09
- Firm location
- Bristol, CT, United States
Product description
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
Data sourced from openFDA. This site is unofficial and independent of the FDA.