Medtronic recalls ILLUMISITE Platform Console Model ILS-1000-CS with 120VAC power cord installed by field service, risking electrical hazards. Affected units have specific serial numbers and UDI-DI codes.
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.
Medtronic is recalling its ILLUMISITE Platform Console (model ILS-1000-CS) because it was improperly converted from 220-240VAC to 120VAC using non-approved power cords and fuses. This could cause electrical hazards if the device is used without proper voltage configuration.
The console was converted from a 220-240VAC model to 120VAC using non-supplied power cords and fuses by Medtronic field service engineers. This improper configuration could lead to electrical issues if the device is used without the correct voltage settings.
Users of the ILLUMISITE Platform Console model ILS-1000-CS with serial number 518503 or UDI-DI code 10884521782211 are affected. Healthcare professionals using this device for medical procedures are most at risk.
Check for the model number ILS-1000-CS on the console. Affected units have a specific serial number (518503) and UDI-DI code (10884521782211).
Verify if the console uses a 120VAC power cord and non-supplied fuses, which may indicate improper conversion.
The console was converted from 220-240VAC to 120VAC using non-supplied power cords and fuses by Medtronic field service engineers, creating an electrical hazard.
Check for model number ILS-1000-CS with serial number 518503 or UDI-DI code 10884521782211.
The recall record does not specify a remedy, so contact Medtronic for guidance on safe handling.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-2008-2023 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-2008-2023 from Medtronic. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
