Covidien, LLC Medtronic ILLUMISITE Platform Console, Model Number ILS-1000-CS Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Medtronic ILLUMISITE Platform Console, Model Number ILS-1000-CS
Brand
Covidien, LLC
Lot Codes / Batch Numbers
UDI-DI: 10884521782211, Serial Number: 518503
Products Sold
UDI-DI: 10884521782211; Serial Number: 518503
Covidien, LLC is recalling Medtronic ILLUMISITE Platform Console, Model Number ILS-1000-CS due to Single ILLUMISITE Platform Console was converted from a 220-240VAC model to a 120VAC configuration using a non-supplied power cord and non-supplied fu. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Covidien notified the single consignee via letter on 05/18/2023. The consignee was instructed to quarantine and return affected product, forward the notification to those who need to be aware within the organization and to any location which the device has been transferred and complete and return the Customer Confirmation Form.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IN
Page updated: Jan 10, 2026