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 15211540 of 27,254 recalls

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 MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion R1.x and R2.x systems Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...

The Issue: A software issue was identified in the internal communication process...

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 L8-4 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 X7-2t 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 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 VL13-5 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 C5-1 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 S7-3t 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 XL14-3 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 L9-3 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 X5-1 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 L12-4 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· Stryker GmbH

Recalled Item: Long Nail Recalled by Stryker GmbH Due to Investigation confirmed that the...

The Issue: Investigation confirmed that the GAMMA4 Right Long Nail was manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2025· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI OneView System BPM Probe: Cat. No. CDI753 - CDI OneView BPM Probe...

The Issue: Due to an error in assembly of the thermistor within some units, the...

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 S8-3t 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 27, 2025· Microbiologics Inc

Recalled Item: KWIK-STICK Recalled by Microbiologics Inc Due to Affected products were...

The Issue: Affected products were packaged with the incorrect KWIK STIK assembly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2025· Medtronic Navigation, Inc.-Boxborough

Recalled Item: O-arm O2 Imaging System. Mobile X-Ray System. Recalled by Medtronic...

The Issue: A mechanical component that supports the O2 gantry to the support structure...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2025· CORIN MEDICAL, LTD.

Recalled Item: Apex Knee System. Model Numbers: KC-50090 Recalled by CORIN MEDICAL, LTD....

The Issue: Investigation has identified that the age of the nylon packaging material...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 23, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: MicroMyst Applicator Recalled by Integra LifeSciences Corp. (NeuroSciences)...

The Issue: Lack of sterility assurance.

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

Class I — Serious Health HazardOngoing