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 22812300 of 46,762 recalls

Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: MR 5300 Recalled by Philips North America Llc Due to Potential...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Ingenia 1.5T Recalled by Philips North America Llc Due to...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2025· Philips North America Llc

Recalled Item: Product Name: Upgrade to MR 7700 Recalled by Philips North America Llc Due...

The Issue: Potential for alignment errors in the cross line functionality when...

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

Class II — Potential Health HazardOngoing
FoodMay 12, 2025· R&M TRADING LLC

Recalled Item: Instant Milk Tea Honeydew Flavor Recalled by R&M TRADING LLC Due to The...

The Issue: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy...

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

Class III — Low RiskOngoing
Refund
FoodMay 12, 2025· R&M TRADING LLC

Recalled Item: Instant Milk Tea Original Flavor Recalled by R&M TRADING LLC Due to The...

The Issue: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy...

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

Class III — Low RiskOngoing
Refund
FoodMay 12, 2025· R&M TRADING LLC

Recalled Item: Instant Milk Tea Brown Sugar Flavor Recalled by R&M TRADING LLC Due to The...

The Issue: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy...

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

Class III — Low RiskOngoing
Refund
FoodMay 12, 2025· R&M TRADING LLC

Recalled Item: Instant Milk Tea Matcha Flavor Recalled by R&M TRADING LLC Due to The...

The Issue: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy...

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

Class III — Low RiskOngoing
Refund
FoodMay 12, 2025· R&M TRADING LLC

Recalled Item: Instant Milk Tea Taro Flavor Recalled by R&M TRADING LLC Due to The Instant...

The Issue: The Instant Milk Tea Powder's ingredients statement declares Non-Dairy...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 12, 2025· HemoCue AB

Recalled Item: The HemoCue Glucose 201 Microcuvettes are designed for use with Recalled by...

The Issue: Glucose microcuvettes experienced transit time outside of limits, so...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2025· Dexcom, Inc.

Recalled Item: Dexcom One+ Continuous Glucose Monitoring System Recalled by Dexcom, Inc....

The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 12, 2025· Dexcom, Inc.

Recalled Item: Dexcom One Continuous Glucose Monitoring System Recalled by Dexcom, Inc. Due...

The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 12, 2025· Dexcom, Inc.

Recalled Item: Dexcom G6 Glucose Receiver Recalled by Dexcom, Inc. Due to Defective foam or...

The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 12, 2025· Dexcom, Inc.

Recalled Item: Dexcom G7 Glucose Receiver Recalled by Dexcom, Inc. Due to Defective foam or...

The Issue: Defective foam or an assembly error may cause the receiver speaker to lose...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 12, 2025· BD SWITZERLAND SARL

Recalled Item: BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP Recalled by BD SWITZERLAND SARL...

The Issue: Sterile, single use closed system drug transfer devices, standalone or on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2025· BD SWITZERLAND SARL

Recalled Item: BD Texium Needle-Free Syringe: 3 mL Recalled by BD SWITZERLAND SARL Due to...

The Issue: Sterile, single use closed system drug transfer devices, standalone or on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2025· Baxter Healthcare Corporation

Recalled Item: Baxter Novum IQ Syringe Pump Recalled by Baxter Healthcare Corporation Due...

The Issue: Baxter has identified a design issue which may cause the pump to detect the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2025· BD SWITZERLAND SARL

Recalled Item: BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP Recalled by BD SWITZERLAND SARL...

The Issue: Sterile, single use closed system drug transfer devices, standalone or on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2025· BD SWITZERLAND SARL

Recalled Item: Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium...

The Issue: Sterile, single use closed system drug transfer devices, standalone or on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2025· BD SWITZERLAND SARL

Recalled Item: BD Texium: 3 mL Recalled by BD SWITZERLAND SARL Due to Sterile, single use...

The Issue: Sterile, single use closed system drug transfer devices, standalone or on...

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

Class II — Potential Health HazardOngoing
DrugMay 9, 2025· AvKARE

Recalled Item: Chlorthalidone Tablets Recalled by AvKARE Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund