ConMed Corporation recalls Arthroscopic Energy 50¿ Probe with Suction, Catalog number: AES-50S Peoduct Usage: For resection, ablation, and coagula…

Recall date

June 17, 2015

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0205-2016

FDA classification

Class II

Brand / firm

ConMed Corporation

Sold / distributed

Worldwide - US distribution in the states of FL, OH, and the country of Spain.

Why it was recalled

Probe programming error. The incorrect program can generate more heat at the surgical site, resulting in an elevated probability of tissue damage.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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.