Discovery MI — Class II medical device recall Z-2580-2018
Terminated recall by GE Healthcare, LLC, reported 2018-08-08, distributed nationwide. Some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired
| Recall number | Z-2580-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Healthcare, LLC, Waukesha, WI, United States |
| Recall initiated | 2018-05-24 |
| Classified | 2018-07-31 |
| Reported by FDA | 2018-08-08 |
| Terminated | 2019-02-08 |
| Distributed | Nationwide (US) |
| Quantity | 42 units |
| Serial numbers | CJRPX1800016CN, CJRPX1800017CN, CJRPX1800018CN, CJRPX1800021CN |
| Model numbers | 5454001-170 |
Product
Discovery MI, labeled as Discovery DMI 15 cm 3 ring, and Discovery DMI 20cm 4 ring
Reason for recall
Some CT and CT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).
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-2580-2018. 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.