Medtronic ILLUMISITE Platform Console — Class II medical device recall Z-2008-2023
Ongoing recall by Covidien, LLC, reported 2023-07-05. Single ILLUMISITE Platform Console was converted from a 220-240VAC model to a 120VAC configuration using a non
| Recall number | Z-2008-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Covidien, LLC, Minneapolis, MN, United States |
| Recall initiated | 2023-05-22 |
| Classified | 2023-06-26 |
| Reported by FDA | 2023-07-05 |
| Countries outside the US | TW |
| Quantity | 1 units |
| UPC / GTIN / UDI-DI | 10884521782211 |
| Serial numbers | 518503 |
| Model numbers | ILS-1000-CS |
Product
Medtronic ILLUMISITE Platform Console, Model Number ILS-1000-CS
Reason for recall
Single ILLUMISITE Platform Console was converted from a 220-240VAC model to a 120VAC configuration using a non-supplied power cord and non-supplied fuses in the field by Medtronic Field Service Engineer.
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-2008-2023. 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.