GE Vingmed Ultrasound As

Complete recall history across all FDA and CPSC categories — 6 total recalls

GE Vingmed Ultrasound As appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (6)

FDA medical device enforcement actions by GE Vingmed Ultrasound As

Date Product Reason Class
May 2, 2024 GE Vivid Ultrasound products, Model Numbers: a) Vivid E90, H45581LB; b) ... GE HealthCare has become aware of an issue with certain Vivid ultrasound syst... Class II
May 2, 2024 GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW GE HealthCare has become aware of an issue with certain Vivid ultrasound syst... Class II
May 30, 2023 GE Healthcare Vivid S60, ultrasound device GE HealthCare has become aware that certain Vivid ultrasound systems cannot b... Class II
May 30, 2023 GE Healthcare Vivid S70, ultrasound device GE HealthCare has become aware that certain Vivid ultrasound systems cannot b... Class II
May 30, 2023 GE Healthcare Vivid S70N, ultrasound device GE HealthCare has become aware that certain Vivid ultrasound systems cannot b... Class II
May 30, 2023 GE Healthcare Vivid S60N, ultrasound device GE HealthCare has become aware that certain Vivid ultrasound systems cannot b... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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