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. 2,480 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,480 in last 12 months

Showing 1522115240 of 46,762 recalls

Medical DeviceMarch 25, 2021· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation Model Number: (9A)9.0.0.113 Recalled by RAYSEARCH LABORATORIES AB...

The Issue: Flags edited in RayCare after a patient has been checked in may not always...

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

Class II — Potential Health HazardOngoing
DrugMarch 24, 2021· Bit & Bet LLC

Recalled Item: Thumbs Up 7 Blue 69K Recalled by Bit & Bet LLC Due to Marketed without...

The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 24, 2021· Pacific Medical Group Inc.

Recalled Item: Aftermarket Alaris Infusion Pump Module Model 8100 Front Bezel Recalled by...

The Issue: Aftermarket front bezel components were installed during service/repair, not...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 24, 2021· Becton Dickinson & Co.

Recalled Item: BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended Recalled...

The Issue: BioGX SARS-CoV-2 Reagents for BD MAX" System rehydration buffer tubes were...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2021· Gf Health Products

Recalled Item: Drop Arm Versamode" Recalled by Gf Health Products Due to The front casters...

The Issue: The front casters on the 6810A Lumex Drop Arm Versamode are incorrect.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2021· Medtronic Inc.

Recalled Item: VenaSeal Closure System Recalled by Medtronic Inc. Due to Firm received...

The Issue: Firm received increased number of reports that VenaSeal dispensing systems...

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

Class III — Low RiskOngoing
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: Saxenda (liraglutide) Injection Recalled by Novo Nordisk Inc Due to...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: NovoLog FlexPen (insulin aspart) Injection Recalled by Novo Nordisk Inc Due...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: OZEMPIC (semaglutide) injection Recalled by Novo Nordisk Inc Due to...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: ViCTOZA (liraglutide) injection Recalled by Novo Nordisk Inc Due to...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: TRESIBA (insulin degludec injection) 100 units/mL (U-100) Recalled by Novo...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Macleods Pharma Usa Inc

Recalled Item: Candesartan Cilexetil Tablets Recalled by Macleods Pharma Usa Inc Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: Fiasp PenFill (insulin aspart injection) 100 units/mL (U-100) Recalled by...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: Xultophy 100/3.6 (insulin degludec and liraglutide injection) Recalled by...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: Levemir FlexTouch (insulin detemir) injection Recalled by Novo Nordisk Inc...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: Fiasp (insulin aspart injection) Recalled by Novo Nordisk Inc Due to...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: Fiasp FlexTouch (insulin aspart injection) 100 units/mL (U-100) Recalled by...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: TRESIBA FlexTouch (insulin degludec injection) 100 units/mL (U-100) Recalled...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: NovoLog (Insulin aspart) Injection Recalled by Novo Nordisk Inc Due to...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 22, 2021· Novo Nordisk Inc

Recalled Item: TRESIBA FlexTouch (insulin degludec injection) 200 units/mL (U-200) Recalled...

The Issue: Temperature Abuse: product samples were stored at temperatures below 32* F...

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

Class I — Serious Health HazardOngoing
Refund