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. 2,487 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,487 in last 12 months

Showing 1330113320 of 46,762 recalls

FoodNovember 20, 2021· RIPPLE FOODS PBC

Recalled Item: Ripple Dairy-Free. As It Should Be 8g Plant Based Protein Recalled by RIPPLE...

The Issue: Complaint led investigation found the presence of Bacillus Cereus in one lot...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 19, 2021· Ascent Pharmaceuticals, Inc.

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets Recalled by Ascent...

The Issue: Product Mix-up

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 19, 2021· American Screening LLC

Recalled Item: AmericanScreening HAND SANITIZER (ethyl alcohol 70%) ANTIMICROBIAL FORMULA...

The Issue: Labeling Not Elsewhere Classified: Hand sanitizer packaged in containers...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 19, 2021· Lupin Pharmaceuticals Inc.

Recalled Item: Tydemy (drospirenone Recalled by Lupin Pharmaceuticals Inc. Due to Subpotent...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
FoodNovember 19, 2021· CONAGRA BRANDS

Recalled Item: Birds Eye Broccoli Tots Recalled by CONAGRA BRANDS Due to Small rocks and...

The Issue: Small rocks and metal fragments in the product

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 19, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Edge Plus-Computed tomography system Model 1026700 Recalled by...

The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS-Computed tomography system Model 8098027 Recalled by...

The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Edge -Computed tomography system Model 10590000 Recalled...

The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2021· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Confidence -Computed tomography systems Model 10590100 Recalled by...

The Issue: Software version VB20_SP5 my lead to a relevant degradation of head image...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2021· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Instructions for Use for all model numbers of the Medtronic Recalled by...

The Issue: There have been reports of stent migration.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 19, 2021· Philips North America Llc

Recalled Item: Philips Allura Xper FD series with Software Version Number: 2.1.x- Recalled...

The Issue: Set screws securing the two gliding rods of the Extra Monitors (called 7th...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer with Software version: V1.25.1 and lower- An...

The Issue: (1)Software (SW) versions V1.25.1 and lower may result in TDef (Test...

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

Class II — Potential Health HazardOngoing
DrugNovember 17, 2021· Blistex Inc

Recalled Item: Odor-Eaters Spray Powder Recalled by Blistex Inc Due to Chemical...

The Issue: Chemical contamination: Presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 17, 2021· Sandoz Inc

Recalled Item: Enoxaparin Sodium Injection Recalled by Sandoz Inc Due to Temperature Abuse;...

The Issue: Temperature Abuse; temperature excursion during shipping

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 17, 2021· Luminex Corporation

Recalled Item: ARIES HSV 1&2 Assay Recalled by Luminex Corporation Due to Impacted lot may...

The Issue: Impacted lot may leak inside the ARIES instrument. Testing confirmed a leak...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2021· Stanley Security Solutions Inc

Recalled Item: Senior Living Arial Emergency and Nurse Call Systems Recalled by Stanley...

The Issue: Systems are not alarming due to increased memory consumption.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2021· Roche Molecular Systems, Inc.

Recalled Item: cobas LiatSystem Recalled by Roche Molecular Systems, Inc. Due to Roche has...

The Issue: Roche has identified a small number of cobas Liat analyzer units that have...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2021· Ohio Medical Corporation

Recalled Item: Instavac Portable Suction Pump Recalled by Ohio Medical Corporation Due to...

The Issue: Increase in premature device failures

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2021· Abbott

Recalled Item: Ultimum HEMOSTASIS INTRODUCER 5f 1.67 MM Recalled by Abbott Due to As a...

The Issue: As a result of a manufacturing error, one (1) lot of Ultimum Hemostasis...

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

Class II — Potential Health HazardOngoing
DrugNovember 15, 2021· Aurobindo Pharma USA Inc.

Recalled Item: Carvedilol Tablets Recalled by Aurobindo Pharma USA Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund