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. 1,741 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,741 in last 12 months

Showing 3682136840 of 47,938 recalls

DrugJune 1, 2015· American Health Packaging

Recalled Item: Zonisamide capsules Recalled by American Health Packaging Due to CGMP...

The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 1, 2015· American Health Packaging

Recalled Item: Azithromycin tablets Recalled by American Health Packaging Due to CGMP...

The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 1, 2015· American Health Packaging

Recalled Item: Lisinopril tablets Recalled by American Health Packaging Due to CGMP...

The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 1, 2015· American Health Packaging

Recalled Item: Lisinopril tablets Recalled by American Health Packaging Due to CGMP...

The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 1, 2015· American Health Packaging

Recalled Item: Azithromycin tablets Recalled by American Health Packaging Due to CGMP...

The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 1, 2015· American Health Packaging

Recalled Item: Amlodipine besylate tablets Recalled by American Health Packaging Due to...

The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 1, 2015· American Health Packaging

Recalled Item: Famotidine tablets Recalled by American Health Packaging Due to CGMP...

The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 1, 2015· American Health Packaging

Recalled Item: Lisinopril tablets Recalled by American Health Packaging Due to CGMP...

The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 1, 2015· American Health Packaging

Recalled Item: Amlodipine besylate tablets Recalled by American Health Packaging Due to...

The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 1, 2015· American Health Packaging

Recalled Item: Lisinopril tablets Recalled by American Health Packaging Due to CGMP...

The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 1, 2015· American Health Packaging

Recalled Item: Azithromycin tablets Recalled by American Health Packaging Due to CGMP...

The Issue: CGMP Deviations: Firm did not adequately investigate customer complaints.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2015· Ungar's Food Products, Inc.

Recalled Item: Dr. Praeger's California Veggie Burgers Gluten Free 11 oz. Manufactured...

The Issue: Dr. Praeger's Gluten Free California Burgers contain undeclared soy.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 1, 2015· Teleflex Medical

Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...

The Issue: The double swivel connector may crack or separate on the endobronchial tube.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2015· Teleflex Medical

Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...

The Issue: The double swivel connector may crack or separate on the endobronchial tube.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2015· Teleflex Medical

Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...

The Issue: The double swivel connector may crack or separate on the endobronchial tube.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2015· Teleflex Medical

Recalled Item: HUDSON RCI Recalled by Teleflex Medical Due to The double swivel connector...

The Issue: The double swivel connector may crack or separate on the endobronchial tube.

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...

The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...

The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Hamilton Medical, Inc.

Recalled Item: Hamilton Medical Infant Flow Sensor Recalled by Hamilton Medical, Inc. Due...

The Issue: An issue has been discovered with the Hamilton Medical Infant Flow Sensor,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2015· Stryker Sustainability Solutions

Recalled Item: Cannula and Seal Recalled by Stryker Sustainability Solutions Due to Stryker...

The Issue: Stryker Sustainability Solutions is recalling Trocars because they have...

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

Class II — Potential Health HazardOngoing