Aesculap Implant Systems LLC: Medical Device Recall in 2017 - (Recall #: Z-1218-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: January 9, 2017

Date Posted: February 22, 2017

Recall Number: Z-1218-2017

Event ID: 76210

Reason for Recall:

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

Status: Terminated

Product Quantity: 24 generators

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

Distribution Pattern:

USA (nationwide Distribution).

Voluntary or Mandated:

Voluntary: Firm initiated