Class II — KENT IMAGING, INC.
| Recalling firm | Kent Imaging Inc. |
|---|---|
| Registered facility | Kent Imaging Inc (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Tissue oxygenation measurement system touchscreens may be unresponsive, which may prevent the viewing of oxygenation images. |
| Product | Snapshot NIR, REF: KD204 |
| Quantity | 57 |
| Distribution | Worldwide - US Nationwide distribution in the states of IN, OH, TX, PA, WI, OR, CO, IL, MO, CA, AZ, IA and the countries of Malaysia. |
| Initiated | 2023-10-30 |
| Classified | 2024-01-25 |
| Recall number | Z-0789-2024 |
| 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 — KENT IMAGING, INC. (Z-0789-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93624/
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