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ConMed Corporation recalls Arthroscopic Energy 50¿ Probe with Suction, Catalog number: AES-50S Peoduct Usage: For resection, ablation, and coag
Recalled November 11, 2015 · FDA recall Z-0205-2016 · ConMed
Hazard
Probe programming error. The incorrect program can generate more heat at the surgical site, resulting in an elevated probability of tissue damage. · FDA Class II
Units
276 devices
Sold at
Worldwide - US distribution in the states of FL, OH, and the country of Spain.
Description
Probe programming error. The incorrect program can generate more heat at the surgical site, resulting in an elevated probability of tissue damage.
Product
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.
Manufacturer(s)
ConMed Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →