Every recall we track for GE Medical Systems Ultrasound & Primary Care Diagnostics, LL — 12 in all — plus the complaints and injury reports the public filed about them.
GE Medical Systems recalls T2100 Microflex Drive Treadmills (model numbers 2026182-002 or 2026182-004) with specific serial numbers due to a performance issue with spare parts that could cause uncontrolled walking belt motion during stress exercise tests.
GE Medical Systems recalls LOGIQ 9 ultrasound systems due to potential power cord breakage exposing electrical conductors, risking shock. Affected units were sold to healthcare providers for medical imaging.
GE Medical Systems recalls Vivid E9 ultrasound systems due to potential power cord breakage exposing electrical conductors, risking shock. Affected units may need repair or replacement.
GE Medical Systems recalls Vivid E80, E90, and E95 ultrasound systems due to potential power cord breakage causing electrical shock. Affected units may need repair or replacement.
GE Medical Systems recalls Vivid 7 ultrasound systems due to potential power cord breakage exposing electrical conductors, risking shock. Affected units may need repair or replacement.
GE Medical Systems recalls Vivid E95 ultrasound systems due to potential power cord breakage exposing electrical conductors, risking shock. Affected units sold to healthcare providers for medical imaging.
GE Medical Systems recalls LOGIQ E9 ultrasound systems due to potential power cord breakage exposing electrical conductors, risking shock. Affected units were sold to healthcare providers for medical imaging.
GE Medical Systems recalls Vivid E80/E90/E95 ultrasound systems due to potential power cord breakage exposing electrical conductors, risking shock. Affected units may need repair or replacement.
GE Medical Systems recalls Vivid E7 ultrasound systems due to potential power cord breakage exposing electrical conductors, risking shock. Affected units may need repair or replacement.
GE Healthcare recalls Prodigy ultrasound devices with specific model numbers due to risk of incorrect patient information being sent to PACS systems during bone density exams.
GE Healthcare recalls Lunar DPX Duo (LU41693) and DPX Bravo (LU41692) ultrasound devices due to potential incorrect patient information in PACS reports, which could lead to misidentification during bone density exams.
GE Healthcare recalls Lunar DPX NT and MD+ ultrasound devices due to risk of sending bone density reports to PACS with wrong patient names. Affected models include LU8230, LU40338, LU42357, LU42369, LU40352. No remedy specified in recall notice.
