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Philips North America Recalls

53 recalls found for Philips North America. Check current safety alerts and related brands before using affected products.
Active recalls
53
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3
HIGH
FDA DEVICE

Philips Ingenia 3.0T CX with MR Elastography (MRE). 1. Model Number (REF): 781271. 2. Model Number (REF): 782105. 510(k) Numbers: K173079, K183063, K193215, K213583, K223458, K251397,...

The potential for stiffness value errors when a specific range of image reconstruction parameters is used in combination with Resoundant's algorithm, leading to the reconstruction voxel size settings in the default MRE scan protocol displaying too small.

Philips North America
The potential
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Health & Personal Care
HIGH
FDA DEVICE

Philips Recalls Spectral CT 7500 Over Fastener Issues

Philips North America recalled three Spectral CT 7500 units on January 7, 2026. The recall affects models with potential fastener issues that could lead to unsecured rotor parts. Patients and healthcare providers should stop using the device immediately.

Philips North America
As part
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Health & Personal Care
HIGH
FDA DEVICE

Philips North America Recalls MR Systems Over Stiffness Value Errors

Philips North America recalled three MR systems on December 3, 2025. The recall affects models with software versions R11.1 and R12.1 due to potential stiffness value errors. Healthcare providers and patients must stop using these devices immediately.

Philips North America
The potential
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Health & Personal Care
HIGH
FDA DEVICE

Philips North America Recalls MR Systems Over Stiffness Value Errors

Philips North America recalled six MR systems on December 3, 2025. The recall affects devices with software versions R11.1 and R12.1 due to potential stiffness value errors. Healthcare providers must stop using the affected units immediately.

Philips North America
The potential
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