Aesculap Bipolar Generator Foot Pedal, Catalog No. GK226, for electrosurgical cutting and coagulation.
Reported: March 6, 2013 Initiated: January 18, 2013 #Z-0887-2013
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.
Details
- Recalling Firm
- Aesculap, Inc.
- Units Affected
- 59
- Distribution
- USA Nationwide Distribution including the states of: AR, CA, FL, IN, IA, KS, MD, MN, MO, OR, TN, TX, VA and WA.
- Location
- Center Valley, PA
Frequently Asked Questions
What product was recalled? ▼
Aesculap Bipolar Generator Foot Pedal, Catalog No. GK226, for electrosurgical cutting and coagulation.. Recalled by Aesculap, Inc.. Units affected: 59.
Why was this product recalled? ▼
The bipolar energy did not stop after release of the foot pedal.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 6, 2013. Severity: Moderate. Recall number: Z-0887-2013.
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