GE Medical Systems Recalls

7 recalls found for GE Medical Systems. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems Recalled 125 Imactis CT-Navigation System Stereotaxic Accessories in 2026

GE Medical Systems recalled 125 Imactis CT-Navigation System stereotaxic accessories distributed worldwide to healthcare facilities. The recall cites a potential mismatch between the simulated needle trajectory and the actual trajectory. Healthcare providers should stop using the devices immediately and follow the manufacturer's recall instructions.

GE Medical Systems
There is
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Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems Recalls Mammography Systems Over Labeling Hazard

GE Medical Systems recalled 1,818 Senographe Pristina mammography systems on October 24, 2025. The recall affects systems due to missing or incorrect X-Ray Warning labels. This nonconformance to FDA regulations poses a high hazard risk.

GE Medical Systems
Some Senographe
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Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems Recalls Ultrasound Device Over Inaccurate Data

GE Medical Systems recalled 65 units of its LOGIQ P10 series ultrasound device on September 18, 2025. The device may show inaccurate liver steatosis measurements, risking inappropriate clinical decisions. Healthcare providers must cease use immediately and follow recall instructions.

GE Medical Systems
The Ultrasound-Guided
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Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems Recalls Ultrasound System Over Inaccurate Measurements

GE Medical Systems recalled 31 LOGIQ P10 R4.5 HD ultrasound systems on September 18, 2025. The devices may display inaccurate liver steatosis data, risking inappropriate clinical decisions. Healthcare providers must stop using these devices immediately.

GE Medical Systems
The Ultrasound-Guided
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Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems Recalls AW Server Models Over Data Security Risk

GE Medical Systems recalled 7,302 AW Server units on September 5, 2025, due to a critical security vulnerability. The flaw could allow unauthorized access to sensitive patient data. Healthcare providers and patients must cease use immediately and follow recall procedures.

GE Medical Systems
Firm has
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Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems Recalls Electrocardiograph Due to Overheating Hazard

GE Medical Systems recalled 29,225 units of the MAC VU360 Acquisition Trunk Cable and Module Holder on August 22, 2025. Users may incorrectly place the Acquisition Module, leading to cable damage and potential overheating. Affected devices were distributed globally, including the U.S. and several other countries.

GE Medical Systems
If a
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Brand Statistics

Total Recalls
7
Pages
1