Recall Z-0887-2013— Aesculap, Inc.
Class II · Terminated
Class II FDA medical device recall by Aesculap, Inc., initiated 2013-01-18, terminated 2014-01-08. FDA's recall record names no specific 510(k) clearance for this event. Product: Aesculap Bipolar Generator Foot Pedal, Catalog No. GK226, for electrosurgical cutting and coagulation.. Reason: The bipolar energy did not stop after release of the foot pedal..
- Recalling firm
- Aesculap, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2013-01-18
- Terminated
- 2014-01-08
- Firm location
- Center Valley, PA, United States
Product description
Aesculap Bipolar Generator Foot Pedal, Catalog No. GK226, for electrosurgical cutting and coagulation.
Reason for recall
The bipolar energy did not stop after release of the foot pedal.
Data sourced from openFDA. This site is unofficial and independent of the FDA.