Z-1218-2017 Class II Terminated

Recalled by Aesculap Implant Systems LLC — Center Valley, PA

Recall Details

Product Type
Devices
Report Date
February 22, 2017
Initiation Date
January 9, 2017
Termination Date
June 14, 2017
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
24 generators

Product Description

GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories

Reason for Recall

Generators may have a faulty component which could impact the proper functioning of the device.

Distribution Pattern

USA (nationwide Distribution).

Code Information

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