Recall Z-2309-2017— Beekley Corporation
Class III · Terminated
Class III FDA medical device recall by Beekley Corporation, initiated 2017-05-08, terminated 2017-06-20. FDA's recall record names no specific 510(k) clearance for this event. Product: Beekley Medical 0-SPOT Mammography Skin Markers REF 652. Reason: Mammography Skin Marker 0 -SPOT (REF 652) product was mis-labeled with A-SPOT (REF 651) labels.
- Recalling firm
- Beekley Corporation
- Classification
- Class III
- Status
- Terminated
- Initiated
- 2017-05-08
- Terminated
- 2017-06-20
- Firm location
- Bristol, CT, United States
Product description
Beekley Medical 0-SPOT Mammography Skin Markers REF 652
Reason for recall
Mammography Skin Marker 0 -SPOT (REF 652) product was mis-labeled with A-SPOT (REF 651) labels
Data sourced from openFDA. This site is unofficial and independent of the FDA.