Reported Feb 22, 2017 · Terminated
GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories
Aesculap Implant Systems LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Aesculap Implant Systems LLC · 3773 Corporate Pkwy · Center Valley, PA · 18034-8217
Is this the product you have?
- GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories
- Lot codes and dates
- Serial #
12291897189819001909191119291930193219341938199319971998199920002029203020312032203720382039204020412042204520462047204820492050205120522168
- Serial #
- Amount recalled
- 24 generators
Where it was sold
- Nationwide
Why it was recalled
Generators may have a faulty component which could impact the proper functioning of the device.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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