Aesculap Implant Systems LLC recalls GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories
- Recall date
- January 9, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1218-2017
- FDA classification
- Class II
- Brand / firm
- Aesculap Implant Systems LLC
- Sold / distributed
- USA (nationwide Distribution).
Why it was recalled
Generators may have a faulty component which could impact the proper functioning of the device.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories
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