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[Recalled] Discovery MI Digital Ready — DIGITAL ReadyCT/PET systems recently installed with a GE supplied A! electrical… | FDA 2018-05-24

recall fda device united-states

The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.

Recall details

ProductDiscovery MI Digital Ready
Brand / manufacturerGE Healthcare, LLC
Categorydevice
Issuing authorityFDA_DEVICE
ReferenceZ-2579-2018
Country of noticeUnited States
Risk levelClass II
Hazard typerecall
Notice date24 May 2018

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: DIGITAL ReadyCT/PET systems recently installed with a GE supplied A! electrical panel may not be properly wired to the partial system UPS (Uninteruptible Power Supply).

This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from GE Healthcare, LLC

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.

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