GE Healthcare, LOGIQ S8 DIAGNOSTIC ULTRASOUND SYSTEM with R1.1.0 Software. Intended for use by a qualified physician for ultrasound evaluation of Fetal; Abdominal; Pediatric; Small Organ; Peripheral Vascular, etc.
FDA Recall Z-1093-2012 · Posted 2012-02-23
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Reason for Recall
Firm Action
Root Cause
Software design
Distribution Pattern
Worldwide Distribution -- US, including the states of NJ, PA, and WI and countries of UNITED KINGDOM, THAILAND, SOUTH KOREA, SLOVENIA, SINGAPORE, ROMANIA, REPUBLIC OF MOLDOVA, POLAND, MALAYSIA, JAPAN, ITALY, INDIA, GERMANY, FRANCE, EUROPE, CZECH REPUBLIC, AUSTRIA, AUSTRALIA, and ARAB EMIRATES.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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