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. 2,535 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,535 in last 12 months

Showing 74017420 of 47,938 recalls

Medical DeviceOctober 18, 2023· AURIS HEALTH INC

Recalled Item: Monarch Platform Recalled by AURIS HEALTH INC Due to Their is the potential...

The Issue: Their is the potential that software issues may result in flipped image of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2023· AURIS HEALTH INC

Recalled Item: Monarch Platform Recalled by AURIS HEALTH INC Due to Their is the potential...

The Issue: Their is the potential that software issues may result in flipped image of...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2023· Microbiologics Inc

Recalled Item: KWIKSTIK Recalled by Microbiologics Inc Due to A complaint investigation...

The Issue: A complaint investigation showed that the bulk pellets (lot 794-142) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2023· Microbiologics Inc

Recalled Item: LYFO-DISK Recalled by Microbiologics Inc Due to A complaint investigation...

The Issue: A complaint investigation showed that the bulk pellets (lot 794-142) were...

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

Class II — Potential Health HazardOngoing
DrugOctober 17, 2023· VistaPharm LLC

Recalled Item: Aminocaproic Acid Oral Solution Recalled by VistaPharm LLC Due to Failed...

The Issue: Failed Excipient Specifications: high content of ethylene glycol (EG)

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

Class III — Low RiskOngoing
Refund
FoodOctober 17, 2023· Braga Fresh Foods

Recalled Item: Wegman's Organics Sweet Kale Chopped Salad Kit Recalled by Braga Fresh Foods...

The Issue: Undeclared egg

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 17, 2023· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS icono (ceiling configuration) Recalled by Siemens Medical Solutions...

The Issue: Potential hardware issue for ARTIS icono ceiling system: collision sensor...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2023· BioFire Diagnostics, LLC

Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel Recalled by BioFire...

The Issue: Routine quality control testing of affected blood culture identification...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2023· BioFire Diagnostics, LLC

Recalled Item: FilmArray TORCH . HTFA-ASY-0104 is the BIOFIRE TORCH Base Recalled by...

The Issue: Due to an increased risk of degradation of the power entry switch resulting...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2023· Zimmer Biomet Spine Inc.

Recalled Item: Vitality Polyaxial Screw Recalled by Zimmer Biomet Spine Inc. Due to Spinal...

The Issue: Spinal fixation system 7.5mmx 50mm screws are packaged with the correct...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Tracheostomy care kits: (1) Medline Tracheostomy Clean and Care Tray...

The Issue: The component tracheostomy brush has a sharp edge at the tip that can...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 16, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Nursing Skills kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due...

The Issue: The component tracheostomy brush has a sharp edge at the tip that can...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 16, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: (1) Nurse Kit Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to The...

The Issue: The component tracheostomy brush has a sharp edge at the tip that can...

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

Class I — Serious Health HazardOngoing
DrugOctober 13, 2023· Dr. Reddy's Laboratories, Inc.

Recalled Item: Montelukast Sodium Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Presence of Foreign Tablet(s)/Capsule(s): A foreign tablet was found in a...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 13, 2023· Select Custom Solutions, LLC

Recalled Item: JayRobb Vanilla Flavored Egg White Protein Powder. Net Weight 24 Recalled by...

The Issue: foreign material - plastic

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 13, 2023· Breas Medical, Inc.

Recalled Item: with Notch 22M/15F sold as part of Breas Medical MPV circuit 2 pc Kits:...

The Issue: Produced with unintended open slits on the side of the mouthpiece body, may...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2023· Baxter Healthcare Corporation

Recalled Item: Novum IQ Syringe infusion system Recalled by Baxter Healthcare Corporation...

The Issue: Baxter is issuing an Urgent Medical Device Correction for the Novum IQ...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 12, 2023· Medtronic Inc

Recalled Item: Medtronic Mo.Ma Ultra Proximal Cerebral Protection Device Recalled by...

The Issue: The Mo.Ma Ultra device manifold is labelled with 2 stickers, an inferior and...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2023· Medtronic Inc

Recalled Item: Medtronic Mo.Ma Ultra Proximal Cerebral Protection Device Recalled by...

The Issue: The Mo.Ma Ultra device manifold is labelled with 2 stickers, an inferior and...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2023· Medtronic Inc

Recalled Item: Medtronic Mo.Ma Ultra Proximal Cerebral Protection Device Recalled by...

The Issue: The Mo.Ma Ultra device manifold is labelled with 2 stickers, an inferior and...

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

Class II — Potential Health HazardOngoing