Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Arthroscopic Energy 50¿ Probe with Suction Recalled by ConMed Corporation Due to Probe programming error. The incorrect program can generate...
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 ConMed Corporation directly.
Affected Products
Arthroscopic Energy 50¿ Probe with Suction, Catalog number: AES-50S Peoduct Usage: For resection, ablation, and coagulation of soft tissue and hemostasis of blood vessels in arthroscopic and orthopedic surgical procedures.
Quantity: 276 devices
Why Was This Recalled?
Probe programming error. The incorrect program can generate more heat at the surgical site, resulting in an elevated probability of tissue damage.
Where Was This Sold?
This product was distributed to 2 states: FL, OH
About ConMed Corporation
ConMed Corporation has 69 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report