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. 1,032 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,032 in last 12 months

Showing 15321–15340 of 47,938 recalls

DrugApril 29, 2021· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 60 Thyroid Tablets Recalled by Acella Pharmaceuticals, LLC Due to...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 29, 2021· Ascend Laboratories LLC

Recalled Item: Olmesartan Medoxomil Tablets Recalled by Ascend Laboratories LLC Due to...

The Issue: Presence of Foreign Tablet/Capsule

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

Class III — Low RiskOngoing
Refund
DrugApril 29, 2021· Acella Pharmaceuticals, LLC

Recalled Item: NP Thyroid 30 Thyroid Tablets Recalled by Acella Pharmaceuticals, LLC Due to...

The Issue: Subpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 29, 2021· Lupin Pharmaceuticals Inc.

Recalled Item: Cefixime for Oral Suspension USP 100 mg/5mL Recalled by Lupin...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 29, 2021· Covidien, LP

Recalled Item: Adult-Pediatric Electrostatic Filter HME Recalled by Covidien, LP Due to The...

The Issue: The company was notified by their supplier of sterilization services for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Covidien, LP

Recalled Item: Mechanical Filter with Connector Small Recalled by Covidien, LP Due to The...

The Issue: The company was notified by their supplier of sterilization services for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic CB10R79R6 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic BB8M63R5 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic CB10R55R5 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic BB9G78R8 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY7M07R6 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic BB7D76R13 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY10J00R12 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY11B40R1 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic CB7J97R8 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY10Z48R2 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY10Y54R4 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Covidien, LP

Recalled Item: HME for Tracheostomized Patients Recalled by Covidien, LP Due to The company...

The Issue: The company was notified by their supplier of sterilization services for...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic CB4W67R20 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2021· Medtronic Perfusion Systems

Recalled Item: Medtronic HY10L28R3 Recalled by Medtronic Perfusion Systems Due to Specific...

The Issue: Specific lots may have been manufactured with insufficient or incomplete welds.

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

Class II — Potential Health HazardOngoing