Class II — Novarad Corporation
| Recalling firm | NOVARAD CORP. |
|---|---|
| Registered facility | NOVARAD CORP. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Potential for images to be flipped while streaming, which could incorrectly display image orientation markers. |
| Product | NovaPACS versions 7.4, 7.5, 7.6, and 8.0, Diagnostic Viewer. Distributed by Novarad Corporation. Picture archiving and communication system (PACS) |
| Quantity | 2695 |
| Distribution | Worldwide distribution including US nationwide. No Canadian distribution. |
| Initiated | 2013-05-09 |
| Classified | 2016-07-11 |
| Terminated | 2016-12-01 |
| Recall number | Z-2151-2016 |
| 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 — Novarad Corporation (Z-2151-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/74556/
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