GN200 Caiman HF generators recall
GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories
Why was GN200 Caiman HF generators recalled?
Generators may have a faulty component which could impact the proper functioning of the device.
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?
Serial # 1229 1897 1898 1900 1909 1911 1929 1930 1932 1934 1938 1993 1997 1998 1999 2000 2029 2030 2031 2032 2037 2038 2039 2040 2041 2042 2045 2046 2047 2048 2049 2050 2051 2052 2168
- Product
- GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories
- Recalling firm
- Aesculap Implant Systems LLC
- Quantity
- 24 generators
- Distribution
- USA (nationwide Distribution).
- Recall date
- February 22, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)