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Aesculap Implant Systems LLC recalls GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories
Recalled February 22, 2017 · FDA recall Z-1218-2017 · Aesculap Implant Systems
Hazard
Generators may have a faulty component which could impact the proper functioning of the device. · FDA Class II
Units
24 generators
Sold at
USA (nationwide Distribution).
Description
Generators may have a faulty component which could impact the proper functioning of the device.
Product
GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories
Manufacturer(s)
Aesculap Implant Systems LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →