Class II — IPG Medical Corporation
| Recalling firm | IPG Medical Corporation |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Software anomaly that causes a false display of error code 5018. |
| Product | Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser. |
| Quantity | 198 units |
| Distribution | US Nationwide distribution in the state of MA. |
| Initiated | 2026-05-05 |
| Classified | 2026-06-24 |
| Recall number | Z-2554-2026 |
| 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 — IPG Medical Corporation (Z-2554-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99064/
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