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 18811900 of 46,762 recalls

Medical DeviceJuly 7, 2025· Siemens Healthcare Diagnostics Inc

Recalled Item: epoc BGEM BUN Test Card [25pk]. Material Number: 10736515. Recalled by...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed that a negative sodium...

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

Class II — Potential Health HazardOngoing
DrugJuly 5, 2025· FDC Limited

Recalled Item: Timolol Maleate Ophthalmic Solution USP Recalled by FDC Limited Due to...

The Issue: Defective Container: spike of the cap becomes lodged in the nozzle of the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

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

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: S9-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: TRANSDUCER L12-5 Transducer Probe Recalled by Philips Ultrasound, Inc Due to...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Orascoptic Surgical Acuity

Recalled Item: Orascoptic Superior Visualization Dragonfly Essentials Kit ( Nose pad...

The Issue: Due to complaints, loupe nose pads containing nickel may cause an allergic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: C6-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: L12-5 38mm Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: C8-4v Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: L9-3 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: X7-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: C8-5 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: mC7-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: X11-4t Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

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

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: C9-3v Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: L12-4 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: BP10-5ec Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: SCNHD LA L7-4 HDI Transducer Probe Recalled by Philips Ultrasound, Inc Due...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: L8-4 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...

The Issue: To provide clarification and labelling to define the useful life of...

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

Class III — Low RiskOngoing