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 19411960 of 46,762 recalls

Medical DeviceJuly 3, 2025· Philips Ultrasound, Inc

Recalled Item: C9-3io 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: L11-3 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: OMNI III TEE 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· Orascoptic Surgical Acuity

Recalled Item: Orascoptic Superior Visualization Custom loupes with Dragonfly frames...

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: D2TCD 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: C5-2 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: L15-7IO TRANSDUCER 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: X7-2t 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: C9-5ec 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· Orascoptic Surgical Acuity

Recalled Item: Orascoptic Superior Visualization Custom loupes configured with Phantom...

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: L17-5 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: C10-3v 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· Orascoptic Surgical Acuity

Recalled Item: Orascoptic Superior Visualization Phantom Essential kit ( Nose pad Recalled...

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: S8-3 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: S12-4 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: S7-2t 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: X3-1 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
FoodJuly 2, 2025· WINDY CITY ORGANICS LLC

Recalled Item: SunBiotics Activated Almonds Infused with Probiotics Recalled by WINDY CITY...

The Issue: Salmonella Contamination. Firm detected salmonella on one batch of our...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 2, 2025· Lupin Pharmaceuticals Inc.

Recalled Item: Amlodipine and Benazepril HCl Capsules USP 2.5 mg/10 mg Recalled by Lupin...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: released with wrong...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 2, 2025· GE Medical Systems, LLC

Recalled Item: GE HealthCare OEC 9800. Recalled by GE Medical Systems, LLC Due to GE...

The Issue: GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in...

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

Class II — Potential Health HazardOngoing