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. 1,836 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,836 in last 12 months

Showing 1690116920 of 47,938 recalls

Medical DeviceOctober 16, 2020· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Zyphr Disposable Cranial Perforator Recalled by Stryker Instruments...

The Issue: Potential for the inner bit to contain a crack, that may or may not be...

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

Class II — Potential Health HazardOngoing
FoodOctober 14, 2020· Hadson (Toko) Trading Co., Inc.

Recalled Item: Eishindo brand "CUP JELLY (MINI) Recalled by Hadson (Toko) Trading Co., Inc....

The Issue: Product is a choking hazard.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 14, 2020· Angiodynamics, Inc.

Recalled Item: Angiodynamics 5F Standard Micro-Introducer Kit - indicated for percutaneous...

The Issue: 5F Micro-Introducer Kits may not contain the correct device, packaged with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2020· Luminex Corporation

Recalled Item: Verigene Processor SP Recalled by Luminex Corporation Due to Luminex has...

The Issue: Luminex has determined that three (3) separate test fixtures used by field...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2020· Luminex Corporation

Recalled Item: Verigene Processor SP Recalled by Luminex Corporation Due to Luminex has...

The Issue: Luminex has determined that three (3) separate test fixtures used by field...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2020· ROi CPS LLC

Recalled Item: Regard - Product Usage: Obstetric Gynecologic specialized manual instrument....

The Issue: Labeling error, incorrect expiration date.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2020· MEDTRONIC ATS MEDICAL, INC.

Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...

The Issue: There is a potential defect in the seals of the sterile barrier pouch used...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2020· MEDTRONIC ATS MEDICAL, INC.

Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...

The Issue: There is a potential defect in the seals of the sterile barrier pouch used...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2020· MEDTRONIC ATS MEDICAL, INC.

Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...

The Issue: There is a potential defect in the seals of the sterile barrier pouch used...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2020· MEDTRONIC ATS MEDICAL, INC.

Recalled Item: Cardioblate CryoFlex Recalled by MEDTRONIC ATS MEDICAL, INC. Due to There is...

The Issue: There is a potential defect in the seals of the sterile barrier pouch used...

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

Class II — Potential Health HazardOngoing
DrugOctober 9, 2020· Jarrow Formulas Inc

Recalled Item: N-A-C (N-Acetyl-L-Cysteine Recalled by Jarrow Formulas Inc Due to Mislabeling

The Issue: Mislabeling of SUS (N-A-C Sustain 600 mg 100 tab) with N-A-C...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 9, 2020· ANI Pharmaceuticals, Inc.

Recalled Item: Dextroamphetamine Saccharate Recalled by ANI Pharmaceuticals, Inc. Due to...

The Issue: Labeling: Incorrect expiration date. Product dated with 24-month expiration...

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

Class III — Low RiskOngoing
Refund
DrugOctober 9, 2020· ANI Pharmaceuticals, Inc.

Recalled Item: Dextroamphetamine Saccharate Recalled by ANI Pharmaceuticals, Inc. Due to...

The Issue: Labeling: Incorrect expiration date. Product dated with 24-month expiration...

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

Class III — Low RiskOngoing
Refund
DrugOctober 9, 2020· ANI Pharmaceuticals, Inc.

Recalled Item: Dextroamphetamine Saccharate Recalled by ANI Pharmaceuticals, Inc. Due to...

The Issue: Labeling: Incorrect expiration date. Product dated with 24-month expiration...

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

Class III — Low RiskOngoing
Refund
DrugOctober 9, 2020· ANI Pharmaceuticals, Inc.

Recalled Item: Dextroamphetamine Saccharate Recalled by ANI Pharmaceuticals, Inc. Due to...

The Issue: Labeling: Incorrect expiration date. Product dated with 24-month expiration...

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

Class III — Low RiskOngoing
Refund
DrugOctober 9, 2020· ANI Pharmaceuticals, Inc.

Recalled Item: Dextroamphetamine Saccharate Recalled by ANI Pharmaceuticals, Inc. Due to...

The Issue: Labeling: Incorrect expiration date. Product dated with 24-month expiration...

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

Class III — Low RiskOngoing
Refund
DrugOctober 9, 2020· ANI Pharmaceuticals, Inc.

Recalled Item: Dextroamphetamine Saccharate Recalled by ANI Pharmaceuticals, Inc. Due to...

The Issue: Labeling: Incorrect expiration date. Product dated with 24-month expiration...

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

Class III — Low RiskOngoing
Refund
FoodOctober 9, 2020· Sauer Brands Inc - SLO

Recalled Item: The Spice Hunter Pumpkin Pie Spice 1.8 oz. Jar Recalled by Sauer Brands Inc...

The Issue: Potential Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 9, 2020· Sauer Brands Inc - SLO

Recalled Item: The Spice Hunter Cayenne Red Pepper 1.8 oz. Jar Recalled by Sauer Brands Inc...

The Issue: Potential Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 9, 2020· Sauer Brands Inc - SLO

Recalled Item: The Spice Hunter Fennel Seeds 1.3 oz. Jar Recalled by Sauer Brands Inc - SLO...

The Issue: Potential Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund