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. 1,909 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,909 in last 12 months

Showing 74817500 of 47,938 recalls

Medical DeviceOctober 6, 2023· Peter Lazic Gmbh

Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...

The Issue: Customer complaint received that reported the applier failed during surgery....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2023· Peter Lazic Gmbh

Recalled Item: D-Clip Standard/Mini Applier Recalled by Peter Lazic Gmbh Due to Customer...

The Issue: Customer complaint received that reported the applier failed during surgery....

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2023· Encore Medical, LP

Recalled Item: Reverse Shoulder System e+ Recalled by Encore Medical, LP Due to Mislabeling

The Issue: Mislabeling

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2023· Encore Medical, LP

Recalled Item: Recalled by Encore Medical, LP Due to Mislabeling

The Issue: Mislabeling

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 5, 2023· Integra LifeSciences Corp.

Recalled Item: CereLink ICP Extension Cable (Extension Cable) Recalled by Integra...

The Issue: Firm is expanding the existing recall RES 90457 for the Cerelink, initiated...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 5, 2023· Siemens Medical Solutions USA, Inc

Recalled Item: Mobilett Mira wireless (VA20) mobile x-ray system(s) Recalled by Siemens...

The Issue: Due to the incorrect mounting of the buzzer component, there is no acoustic...

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

Class II — Potential Health HazardOngoing
DrugOctober 5, 2023· Dollar Tree Distribution, Inc.

Recalled Item: Certain Over-The-Counter (OTC) drug products sold by Family Dollar retail...

The Issue: CGMP Deviations: OTC products were stored outside of labeled temperature...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 5, 2023· CareFusion 303, Inc.

Recalled Item: MEDFLEX Recalled by CareFusion 303, Inc. Due to If "Clear All" selected...

The Issue: If "Clear All" selected medications is selected on patient profile, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Visgeneer, Inc.

Recalled Item: Blood Uric Acid Monitoring System Each kit contains 1 meter Recalled by...

The Issue: Due to products distributed without premarket clearance or approvals.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Visgeneer, Inc.

Recalled Item: Blood Uric Acid Monitoring System Each kit contains 1 meter Recalled by...

The Issue: Due to products distributed without premarket clearance or approvals.

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

Class II — Potential Health HazardOngoing
DrugOctober 4, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Clinical TREAT Antifungal Powder Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: CGMP deviations: the product was shipped from the Manufacturer to a Medline...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 4, 2023· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Bupropion Hydrochloride Extended-Release Tablets USP (SR) Recalled by SUN...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
DrugOctober 4, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: Oxytocin synthetic Recalled by Denver Solutions, LLC DBA Leiters Health Due...

The Issue: Labeling: Not Elsewhere Classified

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

Class III — Low RiskOngoing
Refund
DrugOctober 4, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: VANCOmycin HCI PF Recalled by Denver Solutions, LLC DBA Leiters Health Due...

The Issue: Labeling: Not Elsewhere Classified

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

Class III — Low RiskOngoing
Refund
DrugOctober 4, 2023· Denver Solutions, LLC DBA Leiters Health

Recalled Item: VANCOmycin HCI PF Recalled by Denver Solutions, LLC DBA Leiters Health Due...

The Issue: Labeling: Not Elsewhere Classified

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: FIRST RESPONSE 2 CT Recalled by Family Dollar Stores, Llc. Due to Products...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Edwards Lifesciences, LLC

Recalled Item: TruWave Pressure monitoring set Recalled by Edwards Lifesciences, LLC Due to...

The Issue: Their is the potential for flushing difficulties during setup of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: MEDIC's CHOICE CONTACT LENS SOLUTION 12FLOZ Recalled by Family Dollar...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Edwards Lifesciences, LLC

Recalled Item: FloTrac Sensor Recalled by Edwards Lifesciences, LLC Due to Their is the...

The Issue: Their is the potential for flushing difficulties during setup of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 4, 2023· Family Dollar Stores, Llc.

Recalled Item: CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT Recalled by Family Dollar Stores,...

The Issue: Products were stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing