UnratedMedical device recall · FDA · Published May 22, 2023
Medtronic ILLUMISITE Console Recall: 120VAC Power Cord Risk
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. Read more at govinfonow.com/recall/58138-medtronic-illumisite-console-recall-120vac-power-cord-risk.
“Medtronic ILLUMISITE Console Recall: 120VAC Power Cord Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/58138-medtronic-illumisite-console-recall-120vac-power-cord-risk. Based on FDA recall #Z-2008-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2008-2023%22&limit=1).
The FDA announced on May 22, 2023, that Covidien LLC is recalling one Medtronic ILLUMISITE Platform Console due to an electrical hazard. The agency stated the device was improperly converted from a 220-240VAC model to a 120VAC configuration using non-supplied power cords and fuses.
How to tell if you have it
Brand: Medtronic
Product: ILLUMISITE Platform Console
Model Number: ILS-1000-CS
UDI-DI: 10884521782211
Serial Number: 518503
Quantity: 1 unit
Distribution: Taiwan
The hazard
The single ILLUMISITE Platform Console was converted from a 220-240VAC model to a 120VAC configuration in the field by a Medtronic Field Service Engineer. This conversion used a non-supplied power cord and non-supplied fuses, creating an electrical hazard.
Context
GovInfoNow's records show Covidien LLC has 52 other recalls on record since August 7, 2017. Recent brand recalls include the May 13, 2026, EndoFLIP System recall regarding incorrectly flagged expired catheters and the April 23, 2026, Mon-a-Therm Stethoscope recall for unapproved temperature sensor risks. Other recent recalls of similar products include the December 15, 2025, Philips Allura Xper FD10C Medical System Recall and the October 16, 2025, Canon Vantage Galan 3T Medical Device Recall.
How to tell if you have this one
Check for the model number ILS-1000-CS on the console. Affected units have a specific serial number (518503) and UDI-DI code (10884521782211).
Brand
Medtronic
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Device Configuration
Verify if the console uses a 120VAC power cord and non-supplied fuses, which may indicate improper conversion.
How this recall unfolded
Recall timeline
FDA published this recall 44 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-2008-2023 (May 22, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2008-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.