EasyDiagnost Eleva DRF — Class II medical device recall Z-2523-2020
Terminated recall by Philips North America, LLC, reported 2020-07-15, distributed nationwide. Thermo switches in the main power supply for the system may be incorrectly installed, resulting in a malfuncti
| Recall number | Z-2523-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips North America, LLC, Andover, MA, United States |
| Recall initiated | 2020-06-02 |
| Classified | 2020-07-07 |
| Reported by FDA | 2020-07-15 |
| Terminated | 2021-02-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | PA |
| Quantity | 52 |
| Reason classes | device malfunction |
| Serial numbers | SN16000002, SN16000004, SN16000006, SN16000011, SN16000013, SN16000017, SN16000022, SN16000025, SN16000028, SN16000029, SN16000030, SN16000031, SN16000036, SN16000037, SN16000039, SN16000041, SN16000042, SN16000043, SN16000044, SN16000045, SN16000048, SN16000054, SN16000056, SN17000001, SN17000006 and 27 more |
| Model numbers | 706050 |
Product
EasyDiagnost Eleva DRF, model no. 706050 - Product Usage: X-ray system, diagnostic, general-purpose.
Reason for recall
Thermo switches in the main power supply for the system may be incorrectly installed, resulting in a malfunction.
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-2523-2020. 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.