Recall Z-1787-2014— Beekley Corporation
Class III · Terminated
Class III FDA medical device recall by Beekley Corporation, initiated 2013-06-19, terminated 2014-06-16. FDA's recall record names no specific 510(k) clearance for this event. 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.
- Recalling firm
- Beekley Corporation
- Classification
- Class III
- Status
- Terminated
- Initiated
- 2013-06-19
- Terminated
- 2014-06-16
- Firm location
- Bristol, CT, United States
Product description
Beekley Spots Light Image O-Spots for Mammography Catalog Number: 252 Product Usage: To identify raised moles in Mammography
Reason for recall
Light Image O-Spots Dispenser mislabeled as Soft n' Stretchy Light Image S-Spots
Data sourced from openFDA. This site is unofficial and independent of the FDA.