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 28812900 of 47,938 recalls

Medical DeviceFebruary 24, 2025· Checkpoint Surgical Inc

Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...

The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2025· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....

The Issue: Device is missing the pin in the graft loader component.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2025· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....

The Issue: Device is missing the pin in the graft loader component.

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

Class II — Potential Health HazardOngoing
DrugFebruary 20, 2025· One Source Nutrition, Inc,

Recalled Item: Vitality Recalled by One Source Nutrition, Inc, Due to Undeclared Sildenafil

The Issue: Marketed without an approved NDA/ANDA: Product found to be tainted with...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 20, 2025· Central Admixture Pharmacy Services, Inc.

Recalled Item: PHENYLephrine added to 0.9% sodium chloride Recalled by Central Admixture...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 20, 2025· Orthofix U.S. LLC

Recalled Item: Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device...

The Issue: The product is mislabeled with the incorrect anterior height of 10mm, but...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2025· Microbiologics Inc

Recalled Item: Helix Elite Inactivated Standard: Inactivated Influenza A/B and Respiratory...

The Issue: The RSV target may give a late Ct value and could potentially not pass QC.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2025· Microbiologics Inc

Recalled Item: Helix Elite" Inactivated Standard: Inactivated SARS-CoV-2 Whole Virus...

The Issue: The A549 human cell target (human cells for sample adequacy control) may...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Wayson Hydrocolloid Models: 1) MJ BANDAGE HYDROCOLLOID HEEL OVAL 6CT...

The Issue: There is a potential for the sterility of the device to be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Wayson Hydrocolloid Models: 1) Model Number: CUR5103 Recalled by MEDLINE...

The Issue: There is a potential for the sterility of the device to be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 19, 2025· Calyxo, Inc.

Recalled Item: CVAC Aspiration System Recalled by Calyxo, Inc. Due to Aspiration system,...

The Issue: Aspiration system, for endoscopic examination/treatment of urinary tract and...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 19, 2025· MIM Software Inc

Recalled Item: MIM software Recalled by MIM Software Inc Due to In situations where two...

The Issue: In situations where two images with differing Fields of View (FOV) complete...

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

Class II — Potential Health HazardOngoing
DrugFebruary 18, 2025· Turbare Manufacturing

Recalled Item: Avastin 1.25 mg/0.05 mL in 0.25 mL Syringe Recalled by Turbare Manufacturing...

The Issue: Lack of Assurance of Sterility: due to a quality control process deviation....

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: CURAD Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Alcohol Prep Pads Recalled by MEDLINE INDUSTRIES, LP - Northfield...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· Safecor Health, LLC

Recalled Item: Ergocalciferol - Vitamin D Supplement - 10 mcg (400 Units) Recalled by...

The Issue: Defective Delivery System: Leakage observed after oral solution was...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· Safecor Health, LLC

Recalled Item: Lorazepam 0.5 mg per 0.25 mL Oral Syringe Recalled by Safecor Health, LLC...

The Issue: Defective Delivery System: Leakage observed after oral solution was...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· Safecor Health, LLC

Recalled Item: Ferrous Sulfate 7.5 mg Iron/0.5 mL Oral Syringe Recalled by Safecor Health,...

The Issue: Defective Delivery System: Leakage observed after oral solution was...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· Safecor Health, LLC

Recalled Item: Morphine Sulfate 5 mg per 0.25 mL Oral Syringe Recalled by Safecor Health,...

The Issue: Defective Delivery System: Leakage observed after oral solution was...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2025· Safecor Health, LLC

Recalled Item: Simethicone 20 mg per 0.3 mL Oral Syringe Recalled by Safecor Health, LLC...

The Issue: Defective Delivery System: Leakage observed after oral solution was...

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

Class II — Potential Health HazardOngoing
Refund