GE Healthcare recalls Logiq P6 Premium TruScan ultrasound systems with models BT07 and BT09 due to increased probe-head temperature during specific scans and with certain probes. Affected units have serial numbers listed in the recall notice.
Increased temperature in the probe-head surface with LOGIQ P6 Model BT07 and BT09 scanners when used in specific types of scans and with specific probes.
GE Healthcare is recalling two models of their Logiq P6 Premium TruScan ultrasound systems (BT07 and BT09) because they can overheat during specific types of scans when used with certain probes. This may cause discomfort or injury to the user.
The probe-head surface can become unusually hot during specific ultrasound scans when used with certain probes. This overheating may cause discomfort or minor burns to the user, but it does not typically cause serious injury.
Users of GE Healthcare Logiq P6 Premium TruScan ultrasound systems with models BT07 or BT09 who are performing specific scans with certain probes. Healthcare professionals using these systems are most at risk.
Check if your GE Healthcare Logiq P6 Premium TruScan ultrasound system has model numbers BT07 or BT09. Affected units have specific serial numbers listed in the recall notice.
Review the serial numbers listed in the recall notice to determine if your unit is affected.
Models BT07 and BT09 of the GE Healthcare Logiq P6 Premium TruScan ultrasound systems.
Check if your unit has model numbers BT07 or BT09 and a serial number listed in the provided recall notice.
The recall notice does not specify a remedy, so you should contact GE Healthcare directly for further instructions.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0788-2019 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-0788-2019 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.
