Recall Z-2148-2012— Berchtold Corp.
Class III · Terminated
Class III FDA medical device recall by Berchtold Corp., initiated 2012-07-10, terminated 2013-06-06. FDA's recall record names no specific 510(k) clearance for this event. Product: Chromovision High Definition (HD) Wireless Camera, Pt # CC-9715900. Visual recording of surgical procedures.. Reason: Defective camera: There is a possibility that the connection of the wires to the connector may become loose, causing image distortion or loss..
- Recalling firm
- Berchtold Corp.
- Classification
- Class III
- Status
- Terminated
- Initiated
- 2012-07-10
- Terminated
- 2013-06-06
- Firm location
- N Charleston, SC, United States
Product description
Chromovision High Definition (HD) Wireless Camera, Pt # CC-9715900. Visual recording of surgical procedures.
Reason for recall
Defective camera: There is a possibility that the connection of the wires to the connector may become loose, causing image distortion or loss.
Data sourced from openFDA. This site is unofficial and independent of the FDA.