Class II — ConMed Corporation
| Recalling firm | CONMED CORPORATION |
|---|---|
| Registered facility | View this company's 6 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | 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. |
| Quantity | 276 devices |
| Distribution | Worldwide - US distribution in the states of FL, OH, and the country of Spain. |
| Initiated | 2015-06-17 |
| Classified | 2015-11-03 |
| Terminated | 2017-04-11 |
| Recall number | Z-0205-2016 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — ConMed Corporation (Z-0205-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/71518/
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