GE Healthcare recalls Vscan Extend devices sold as 'Vscan Extend Dual USB' that won't power on due to battery issues when not turned off before removal or computer connection without AC power.
The firm identified that the Vscan Extend device will not power on because of depleted battery, due to the device not being turned off prior to battery removal or when being connected to a computer without AC power.
GE Healthcare is recalling Vscan Extend ultrasound devices sold as 'Vscan Extend Dual USB' because they may not power on when the battery is removed or connected to a computer without AC power. This could cause the device to fail during use.
The device may not power on when the battery is removed or connected to a computer without AC power, which can cause the device to fail during use. This is a battery-related issue that does not pose a risk of injury.
Users of GE Vscan Extend ultrasound devices sold as 'Vscan Extend Dual USB' who have the specific serial numbers listed in the recall. Most users are healthcare professionals or medical facilities.
Check the serial number (UDI, Model Number) on the device. The affected models include VH1602482A, VH160398U2, VH160910MS, and other specific serial numbers listed in the recall.
Look for the serial number (UDI, Model Number) on the device to confirm if it's in the list of affected models.
The device may not power on due to battery issues when not turned off before removal or connected to a computer without AC power. Check the serial number to see if it's affected.
The recall does not specify a remedy, so no action is required unless the device is affected. Check the serial number to confirm.
The hazard described does not involve injury risk; it only affects the device's ability to power on.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0520-2022 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-0520-2022 from GE Healthcare. 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.
