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 1362113640 of 46,762 recalls

Medical DeviceOctober 15, 2021· Medtronic Vascular, Inc.

Recalled Item: Endurant IIs Stent Graft System REF/Description: ESBF2814C103EE STENT GRAFT...

The Issue: Due to, during stent graft deployment, the spindle may detach from the...

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

Class II — Potential Health HazardOngoing
FoodOctober 14, 2021· KEURIG DR PEPPER

Recalled Item: Target Good & Gather Coconut Pineapple Sparkling Water 8 pack Recalled by...

The Issue: The company has received off flavor and off aroma complaints identified with...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 14, 2021· KEURIG DR PEPPER

Recalled Item: 7UP Zero Sugar Lemon Lime Soda 12 pack of 12 Recalled by KEURIG DR PEPPER...

The Issue: The company has received off flavor and off aroma complaints identified with...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 14, 2021· KEURIG DR PEPPER

Recalled Item: Polar Black Cherry Premium Seltzer 12 pack of 12oz cans Recalled by KEURIG...

The Issue: The company has received off flavor and off aroma complaints identified with...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 14, 2021· KEURIG DR PEPPER

Recalled Item: Target Good & Gather Mixed Berry Sparkling Water 8 pack Recalled by KEURIG...

The Issue: The company has received off flavor and off aroma complaints identified with...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 14, 2021· SEDECAL SA

Recalled Item: MobileDiagnost wDR Recalled by SEDECAL SA Due to While cleaning or...

The Issue: While cleaning or disinfecting the system, if the process is not followed as...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2021· Hill-Rom Inc.

Recalled Item: These are communication systems Recalled by Hill-Rom Inc. Due to An...

The Issue: An unrecoverable error may occur where a component will fail to complete the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2021· Lumenis, Inc.

Recalled Item: IPL Coupling Gel Recalled by Lumenis, Inc. Due to Ultrasound gels and...

The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 14, 2021· FujiFilm Healthcare Americas Corporation

Recalled Item: Arietta 850 Ultrasound- Software Version: V1.0.0 through V4.1.3 Recalled by...

The Issue: Diagnostic ultrasound system with the specified software version and used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2021· FujiFilm Healthcare Americas Corporation

Recalled Item: Lisendo 880 Ultrasound Software Version: V1.0 through V4.1.3 Recalled by...

The Issue: Diagnostic ultrasound system with the specified software version and used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2021· FujiFilm Healthcare Americas Corporation

Recalled Item: Arietta 750 Ultrasound Software Version: V1.0.0 through V2.1.3 Recalled by...

The Issue: Diagnostic ultrasound system with the specified software version and used in...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2021· FujiFilm Healthcare Americas Corporation

Recalled Item: Arietta 65 Ultrasound Software Versions: V1.0 through V4.0.0 Recalled by...

The Issue: When the ultrasound system is used in combination with a Fujifilm (formally...

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

Class II — Potential Health HazardOngoing
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: Advance Formula Pain Reliever (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: Afassco Pain Free Plus X-STRENGTH PAIN RELIEVER (Acetaminophen 250...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: Vica-Cet BACK PAIN RELIEF (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: ZEE+ painaid ESF Extra-Strength Formula (Acetaminophen 250 mg Recalled by...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: AERO Tab PAIN RELIEVER (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: North by Honeywell PAIN STOPPER EXTRA STRENGTH (Acetaminophen 250 mg...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: Xpect First aid Extra Strength PAIN AWAY (Acetaminophen 250 mg/Aspirin...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: PainAway II (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund