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. 2,553 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,553 in last 12 months

Showing 45614580 of 27,512 recalls

Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation Auxiliary 4000 . Intended to securely Recalled by...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation ES (Med ES Main) . Intended Recalled by CareFusion 303,...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· Siemens Medical Solutions USA, Inc.

Recalled Item: ACUSON Maple Diagnostic Ultrasound System Recalled by Siemens Medical...

The Issue: On ultrasound systems, when Cardiac DICOM SR feature is configured to...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation Auxiliary ES . Intended to securely Recalled by...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2024· CareFusion 303, Inc.

Recalled Item: BD Pyxis MedStation 4000 . Intended to securely store Recalled by CareFusion...

The Issue: Retroactive-Due to increase in complaints, their is a potential for drawer...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Baxter Healthcare Corporation

Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...

The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Baxter Healthcare Corporation

Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...

The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Baxter Healthcare Corporation

Recalled Item: Surgical Tools and Cardiovascular Specialty marketing brochures Recalled by...

The Issue: The Surgical Tools and Cardiovascular Specialty marketing brochures...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 22, 2024· Bolton Medical Inc.

Recalled Item: RELAY PRO Thoracic Stent-Graft System Recalled by Bolton Medical Inc. Due to...

The Issue: The stent-graft inside the delivery system was the incorrect size.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Bruder Healthcare Company, LLC

Recalled Item: Thermalon Sinus Compress Recalled by Bruder Healthcare Company, LLC Due to...

The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Alcon Research, LLC

Recalled Item: SYRINGE Recalled by Alcon Research, LLC Due to Medline Bulb irrigation...

The Issue: Medline Bulb irrigation syringes recalled due to potential for packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Abbott Laboratories

Recalled Item: ARCHITECT STAT Myoglobin Reagent Kit Recalled by Abbott Laboratories Due to...

The Issue: The reason for the recall is the failure of calibration and quality controls...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Bruder Healthcare Company, LLC

Recalled Item: MediBeads Neck Wrap Recalled by Bruder Healthcare Company, LLC Due to...

The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Bruder Healthcare Company, LLC

Recalled Item: Thermalon Sinus Compress (French) Recalled by Bruder Healthcare Company, LLC...

The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· InfuTronix LLC

Recalled Item: Nimbus Administration Set Recalled by InfuTronix LLC Due to InfuTronix is...

The Issue: InfuTronix is removing the Nimbus Infusion Pump Systems from the market due...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 21, 2024· Bruder Healthcare Company, LLC

Recalled Item: Thermalon Neck Wrap Recalled by Bruder Healthcare Company, LLC Due to...

The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Covidien

Recalled Item: Situate Laparotomy Sponge Recalled by Covidien Due to Packs including 5...

The Issue: Packs including 5 laparotomy sponges may contain incorrect product with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Bruder Healthcare Company, LLC

Recalled Item: Thermalon Stye Compress Recalled by Bruder Healthcare Company, LLC Due to...

The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Puritan Medical Products Company, Llc

Recalled Item: HydroFlock Sterile Flocked Collection Device Recalled by Puritan Medical...

The Issue: It was discovered through a customer complaint that mislabeled product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 21, 2024· Bruder Healthcare Company, LLC

Recalled Item: Thermalon Eye Compress Recalled by Bruder Healthcare Company, LLC Due to...

The Issue: Thermalon and MediBeads moist heat compresses from certain lots may have...

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

Class II — Potential Health HazardOngoing