Product Recalls in North Dakota

Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,573 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,573 in last 12 months

Showing 14611480 of 47,938 recalls

DrugAugust 28, 2025· Granules Pharmaceuticals Inc.

Recalled Item: Dextroamphetamine Saccharate Recalled by Granules Pharmaceuticals Inc. Due...

The Issue: Failed Impurities/Degradation Specifications:

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

Class III — Low RiskOngoing
Refund
DrugAugust 28, 2025· Granules Pharmaceuticals Inc.

Recalled Item: Dextroamphetamine Saccharate Recalled by Granules Pharmaceuticals Inc. Due...

The Issue: Failed Impurities/Degradation Specifications:

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

Class III — Low RiskOngoing
Refund
DrugAugust 28, 2025· Granules Pharmaceuticals Inc.

Recalled Item: Dextroamphetamine Saccharate Recalled by Granules Pharmaceuticals Inc. Due...

The Issue: Failed Impurities/Degradation Specifications:

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

Class III — Low RiskOngoing
Refund
DrugAugust 28, 2025· Granules Pharmaceuticals Inc.

Recalled Item: Dextroamphetamine Saccharate Recalled by Granules Pharmaceuticals Inc. Due...

The Issue: Failed Impurities/Degradation Specifications:

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

Class III — Low RiskOngoing
Refund
DrugAugust 28, 2025· Ascend Laboratories, LLC

Recalled Item: Aripiprazole Tablets Recalled by Ascend Laboratories, LLC Due to Superpotent...

The Issue: Superpotent drug

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 28, 2025· Vantive US Healthcare LLC

Recalled Item: Sharesource Connectivity Platform for Use with Homechoice Claria Product...

The Issue: Vantive has identified a software defect within the Sharesource Claria...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: Biograph mMR. Model Number: 10433372. Recalled by Siemens Medical Solutions...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Prisma. Model Number: 10849582. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: BIOGRAPH One (DE). Model Number: 11689172. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Verio. Model Number: 10276755. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Lumina (DE). Model Number: 11344916. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Spectra as the following: 1. MAGNETOM Spectra. Model Number:...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra Fit BioMatrix. Model Number: 11516217. Recalled by Siemens...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396 Recalled by...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Vida Fit. Model Number: 11410481. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Skyra fit. Model Number: 10849580. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Cima.X (DE). Model Number: 11647158. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Verio Dot Upgrade. Model Number: 10684334. Recalled by Siemens...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 28, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: MAGNETOM Connectom.X. Model Number: 11371480. Recalled by Siemens Medical...

The Issue: There is a potential for an ice blockage to form or currently exist within...

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

Class I — Serious Health HazardOngoing