ProxiDiagnost N90 — Class II medical device recall Z-3023-2020
Terminated recall by Philips North America, LLC, reported 2020-10-07. Unexpected increase in peak tube potential (kV) will lead to an increased patient radiation dose.
| Recall number | Z-3023-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | FDA mandated |
| Recalling firm | Philips North America, LLC, Andover, MA, United States |
| Recall initiated | 2019-11-20 |
| Classified | 2020-09-30 |
| Reported by FDA | 2020-10-07 |
| Terminated | 2024-04-04 |
| Quantity | 71 |
Product
ProxiDiagnost N90
Reason for recall
Unexpected increase in peak tube potential (kV) will lead to an increased patient radiation dose.
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-3023-2020. 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.