FDA Device recall Z-2008-2023
Medtronic ILLUMISITE Platform Console, Model Number ILS-1000-CS
- FDA Device
- Class II
- ongoing
- Published 2023-07-05
On 2023-07-05 the FDA classified a Class II recall of Medtronic ILLUMISITE Platform Console, Model Number ILS-1000-CS by Covidien, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2008-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-05-22 |
| Published | 2023-07-05 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Covidien |
| Distribution | n/a |
Product
Medtronic ILLUMISITE Platform Console, Model Number ILS-1000-CS
Reason
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.
Identifiers
| code_info | UDI-DI: 10884521782211; Serial Number: 518503 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2008-2023%22
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