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. 2,531 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,531 in last 12 months

Showing 96819700 of 47,938 recalls

FoodFebruary 21, 2023· Chukar Cherry Company Inc.

Recalled Item: Chukar Cherries Cherry Bombs Bits 'n Pieces Recalled by Chukar Cherry...

The Issue: undeclared hazelnuts

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 21, 2023· Bio-Rad Laboratories, Inc.

Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to Bio-Rad received...

The Issue: Bio-Rad received four customer complaints from 11/30/2022 to 12/21/2022 on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Bio-Rad Laboratories, Inc.

Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to Bio-Rad received...

The Issue: Bio-Rad received four customer complaints from 11/30/2022 to 12/21/2022 on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Biosense Webster, Inc.

Recalled Item: Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath Recalled by...

The Issue: Incorrect labeling; specifically, the product name, lot number and product...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Biosense Webster, Inc.

Recalled Item: Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath Recalled by...

The Issue: Incorrect labeling; specifically, the product name, lot number and product...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis Lysis Beads Recalled by Entopsis , Inc. Due to Presence of...

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Preat Corp

Recalled Item: Neodent GM X 6mm Engaging Titanium Base Recalled by Preat Corp Due to...

The Issue: Engaging titanium base contains a dimensional condition that allows vertical...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis Reagent RVD with RVD Enhancer: a) 1 mL Recalled by Entopsis , Inc....

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis BCSNano (1mL) Recalled by Entopsis , Inc. Due to Presence of...

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis Support: a) 1 mL Recalled by Entopsis , Inc. Due to Presence of...

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis Reagent RVD-RT Recalled by Entopsis , Inc. Due to Presence of...

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis Activator: a) 1.5mL Recalled by Entopsis , Inc. Due to Presence of...

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2023· Entopsis , Inc.

Recalled Item: PCRopsis Reagent Buccal Recalled by Entopsis , Inc. Due to Presence of...

The Issue: Presence of misleading label statements on the product label.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2023· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: SmartPerfusion Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: There are technical issues related to signal generation and processing,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2023· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: 2D Perfusion Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to There...

The Issue: There are technical issues related to signal generation and processing,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2023· Moberg Research, Inc.

Recalled Item: Moberg Component Neuromonitoring System (CNS Monitor)-Intended as a...

The Issue: Battery leakage can cause corrosion to the metal enclosure near the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 17, 2023· Akron Pharma, Inc.

Recalled Item: DIBUCAINE 1% HEMORRHOIDAL OINTMENT Recalled by Akron Pharma, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date

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

Class III — Low RiskOngoing
Refund
DrugFebruary 17, 2023· Sciegen Pharmaceuticals Inc

Recalled Item: Gabapentin Tablets Recalled by Sciegen Pharmaceuticals Inc Due to Presence...

The Issue: Presence of Foreign Tablets/Capsules: Pharmacist reported presence of some...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 17, 2023· BINDLE BOTTLE

Recalled Item: Stainless Steel Water Bottle The product comes in four sizes: 32 oz....

The Issue: Water bottle has a cup with a screw cap attached by a weld that has been...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 17, 2023· AGILENT TECHNOLOGIES INC./US

Recalled Item: Agilent Resolution ctDx FIRST Sample Collection Kit Recalled by AGILENT...

The Issue: Distributed sample collection kit with an unapproved instruction for use.

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

Class III — Low RiskOngoing