Product Recalls in Alaska

Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,550 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,550 in last 12 months

Showing 15011520 of 27,254 recalls

Medical DeviceMay 30, 2025· Maquet Critical Care AB

Recalled Item: Servo-u Ventilator System. Model Number: 6688600. Recalled by Maquet...

The Issue: Potential for inaccurate measurement of the patient circuit compliance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 30, 2025· Maquet Critical Care AB

Recalled Item: Servo-n Ventilator System. Model Number: 6694800. Recalled by Maquet...

The Issue: Potential for inaccurate measurement of the patient circuit compliance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 30, 2025· Maquet Critical Care AB

Recalled Item: Servo-u MR Ventilator System. Model Number: 6888800. Recalled by Maquet...

The Issue: Potential for inaccurate measurement of the patient circuit compliance...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Intera 1.5T Achieva Nova-Dual Product Number: 781173 Recalled by Philips...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Intera 1.5T Explorer/Nova Dual Product Number: 781108 Recalled by Philips...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: SmartPath to dStream for 1.5T¿ Recalled by Philips North America Due to...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Intera 1.5T Achieva IT Nova Product Number: 781175 Recalled by Philips North...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Intera 1.5T Achieva Nova Product Number: 781172 Recalled by Philips North...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Intera Achieva 1.5T Pulsar Recalled by Philips North America Due to...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Intera 1.5T Master/Nova Product Number: 781106 Recalled by Philips North...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Intera 1.5T Omni/Stellar Recalled by Philips North America Due to identified...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2025· Philips North America

Recalled Item: Achieva XR Product Numbers: (1) 781153 Recalled by Philips North America Due...

The Issue: identified an issue where a component failure in the specific Gradient Coil...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips eL18-4 EMT Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips C9-5EC Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips eL18-4 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips C5-2 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips L12-3 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips X6-1 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips X8-2t Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Philips Ultrasound, Inc

Recalled Item: Philips V6-2 Transducer. Recalled by Philips Ultrasound, Inc Due to...

The Issue: Ultrasound transducer devices were beyond their useful life.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing