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. 2,417 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,417 in last 12 months

Showing 1956119580 of 46,762 recalls

Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Transducer w/wing 5700LAX...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Transducer w/knob...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical Philips M1355A Toco Transducer with belt wire/knob Recalled...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical Philips M1356A Ultrasound Transducer with belt/wire knob...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Toco Transducer w/wing (2264LAX)...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob Recalled by...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Recalled by Pacific...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· CrossRoads Extremity Systems, LLC

Recalled Item: MotoBand CP Recalled by CrossRoads Extremity Systems, LLC Due to Potentially...

The Issue: Potentially includes a 3.0mm x 30mm screw instead of 3.0mm x 28mm screw.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...

The Issue: An issue with the Detector for the Forte Family of cameras may result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...

The Issue: An issue with the Detector for the Forte Family of cameras may result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...

The Issue: An issue with the Detector for the Forte Family of cameras may result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...

The Issue: An issue with the Detector for the Forte Family of cameras may result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...

The Issue: An issue with the Detector for the Forte Family of cameras may result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2019· Baxter Healthcare Corporation

Recalled Item: TherMax Blood Warmer Unit Recalled by Baxter Healthcare Corporation Due to...

The Issue: TherMax Blood Warmers may not be in compliance with an electrical safety...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Xodus Medical Inc

Recalled Item: Electrosurgical Tip Cleaner Product Usage: electrosurgical accessory...

The Issue: The sterile barrier of some devices may have been affected

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Xodus Medical Inc

Recalled Item: Cautery Tip Cleaner Product Usage: electrosurgical accessory Recalled by...

The Issue: The sterile barrier of some devices may have been affected

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Xodus Medical Inc

Recalled Item: Electrosurgical Tip Cleaner Product Usage: electrosurgical accessory...

The Issue: The sterile barrier of some devices may have been affected

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

Class II — Potential Health HazardOngoing
DrugSeptember 18, 2019· Avella of Deer Valley, Inc. Store 38

Recalled Item: Povidone Iodine Recalled by Avella of Deer Valley, Inc. Store 38 Due to Lack...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 18, 2019· GCP Laboratories Inc

Recalled Item: Major Infants' Gas Relief Drops Recalled by GCP Laboratories Inc Due to...

The Issue: Microbial Contamination of Non-Sterile Product.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 18, 2019· Wismettac Asian Foods, INC

Recalled Item: Shirakiku Buckwheat Noodles Yamaimo Soba With Concentration Soup Base...

The Issue: Product label identifies bonito, but product dipping sauce actually contains...

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

Class II — Potential Health HazardOngoing
Refund