Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GN200 Caiman HF generators Recalled by Aesculap Implant Systems LLC Due to Generators may have a faulty component which could...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Aesculap Implant Systems LLC directly.
Affected Products
GN200 Caiman HF generators, electrosurgical, cutting & coagulation & accessories
Quantity: 24 generators
Why Was This Recalled?
Generators may have a faulty component which could impact the proper functioning of the device.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Aesculap Implant Systems LLC
Aesculap Implant Systems LLC has 61 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report