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LELTEK

LELTEK INC. · Model LX128LC · UDI-DI 04719882150197

IYNITXIYO Prescription
10
510(k) clearances
2,691
Adverse events (35 deaths)
299
Recalls
222
Facilities

Description

The Ultrasound Imaging System is a software-based imaging system and accessories intended for use by qualified physicians and healthcare professionals who has the ability to conduct ultrasound scan process for evaluation by ultrasound imaging system or fluid flow analysis of the human body. The modes of operation include B mode, M mode, PWD mode, Color Doppler (CD) mode, Power Doppler mode, and the combined mode (B+M, B+CD, B+PWD).

Recalls

DateFirmReason
2026-08-07Philips Ultrasound, LLCDue to software issue with ultrasound system, doppler sample is displayed shallower than its actual measurement location, potentially causing inaccurate blood flow velocity measure
2025-10-31Philips Ultrasound, LLCUltrasound system compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imagining.
2025-10-09B-K Medical A/SGE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-lif
2025-10-09B-K Medical A/SGE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-lif
2025-10-09B-K Medical A/SGE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-lif
2025-10-09B-K Medical A/SGE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-lif
2025-10-09B-K Medical A/SGE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-lif
2025-10-09B-K Medical A/SGE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-lif
2025-09-18GE Medical Systems, LLCThe Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinica
2025-09-18GE Medical Systems, LLCThe Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinica

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.