FDAFDA · Food and drugs·Recall number Z-1218-2017
GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories
Published February 22, 2017 · Recall initiated: January 9, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Generators may have a faulty component which could impact the proper functioning of the device.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Aesculap Implant Systems LLC
- Distributor
- USA (nationwide Distribution).
- Lot
- 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
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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