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. 1,984 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,984 in last 12 months

Showing 71217140 of 47,938 recalls

DrugNovember 13, 2023· KINDER FARMS LLC

Recalled Item: KinderMed KIDS' PAIN & FEVER Acetaminophen Recalled by KINDER FARMS LLC Due...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 13, 2023· KINDER FARMS LLC

Recalled Item: KinderMed INFANTS' PAIN & FEVER Acetaminophen Recalled by KINDER FARMS LLC...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 13, 2023· Kilitch Healthcare India Limited

Recalled Item: Lubricant Eye Drops (Propylene glycol 0.6%) Recalled by Kilitch Healthcare...

The Issue: Non-Sterility

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 10, 2023· Golden State Medical Supply Inc.

Recalled Item: PAROXETINE tablets Recalled by Golden State Medical Supply Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc....

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 10, 2023· Teva Pharmaceuticals USA, Inc

Recalled Item: Testosterone Gel Recalled by Teva Pharmaceuticals USA, Inc Due to OOS for...

The Issue: OOS for viscosity

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

Class III — Low RiskOngoing
Refund
DrugNovember 10, 2023· Fagron Compounding Services

Recalled Item: Tropicamide 1% (10mg/mL) Recalled by Fagron Compounding Services Due to...

The Issue: Labeling: Label Mix-Up: The label of a dropper bottle mistakenly states the...

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

Class III — Low RiskOngoing
Refund
DrugNovember 10, 2023· Golden State Medical Supply Inc.

Recalled Item: PAROXETINE tablets Recalled by Golden State Medical Supply Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc....

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 10, 2023· Golden State Medical Supply Inc.

Recalled Item: PAROXETINE tablets Recalled by Golden State Medical Supply Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications-Manufacturer Apotex Inc....

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Wire Guided Balloon 13.5-14.5-15.5. Indicated for endoscopic...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Wire Guided Balloon 6-7-8. indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Fixed Wire Balloon 6-7-8. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Fixed Wire Balloon 13.5-14.5-15.5. Indicated for endoscopic...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Wire Guided Balloon 16-17-18. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Fixed Wire Balloon 16-17-18. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Encore Medical, LP

Recalled Item: DJO surgical EMPOWR Porous Knee System Empowr 3D Femur-Porous Coated...

The Issue: Due to incorrect product/device within packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Smiths Medical Asd Inc

Recalled Item: Medex LOGICAL CATH LAB KIT Recalled by Smiths Medical Asd Inc Due to There...

The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Fixed Wire Balloon 11-12-13. Indicated for endoscopic dilation of...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Olympus Corporation of the Americas

Recalled Item: EZDilate Fixed Wire Balloon 8.5-9.5-10.5. Indicated for endoscopic dilation...

The Issue: Product balloon issues: inflating, deflating and/or retrieving the devices;...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Smiths Medical Asd Inc

Recalled Item: 6IN PRESSURE TUBING Recalled by Smiths Medical Asd Inc Due to There is a...

The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2023· Smiths Medical Asd Inc

Recalled Item: 20IN (50.8CM) BRAIDED INJ LINE Recalled by Smiths Medical Asd Inc Due to...

The Issue: There is a manufacturing defect affecting specific rotator lots. Within this...

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

Class II — Potential Health HazardOngoing