Arthroscopic Energy 50¿ Probe with Suction — Class II medical device recall Z-0205-2016
Terminated recall by ConMed Corporation, reported 2015-11-11, distributed in FL, OH. Probe programming error. The incorrect program can generate more heat at the surgical site, resulting in an el
| Recall number | Z-0205-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ConMed Corporation, Utica, NY, United States |
| Recall initiated | 2015-06-17 |
| Classified | 2015-11-03 |
| Reported by FDA | 2015-11-11 |
| Terminated | 2017-04-11 |
| Distributed | FL, OH |
| Countries outside the US | ES |
| Quantity | 276 devices |
| Model numbers | AES-50S |
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.
Reason for recall
Probe programming error. The incorrect program can generate more heat at the surgical site, resulting in an elevated probability of tissue damage.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0205-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.