Aesculap GNI161 Bipolar Foot Control Product Usage: The recall
Aesculap GNI161 Bipolar Foot Control Product Usage: The Aesculap Bipolar Coagulator is intended for use in surgery to generate electrical power for…
Why was Aesculap GNI161 Bipolar Foot Control Product Usage: The recalled?
Complaints were received for the GN161 Bipolar Foot Control reporting that the bipolar energy did not stop after release of the foot control.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
all GN161's distributed between 4/28/2009 and 5/22/2013.
- Product
- Aesculap GNI161 Bipolar Foot Control Product Usage: The Aesculap Bipolar Coagulator is intended for use in surgery to generate electrical power for…
- Recalling firm
- Aesculap, Inc.
- Quantity
- 85
- Distribution
- Worldwide Distribution - USA Nationwide and countries of: Austria, Germany, Japan, and Taiwan.
- Recall date
- December 18, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)