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. 1,065 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,065 in last 12 months

Showing 2761–2780 of 47,938 recalls

DrugMarch 7, 2025· Direct Rx

Recalled Item: Duloxetine D/R Recalled by Direct Rx Due to CGMP Deviations: Presence of...

The Issue: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 7, 2025· Ethicon Endo Surgery, LLC

Recalled Item: PDS¿PLUS¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1¿MP Recalled by Ethicon Endo...

The Issue: Identified curing issues with the silicone during the needles manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2025· GE Medical Systems, LLC

Recalled Item: Venue Fit Models: R3 (Model Number H45303VFSC Recalled by GE Medical...

The Issue: The battery for certain ultrasound systems can potentially develop an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2025· GE Medical Systems, LLC

Recalled Item: Venue Go Models: R2 (Model Number H45181VG) Recalled by GE Medical Systems,...

The Issue: The battery for certain ultrasound systems can potentially develop an...

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

Class II — Potential Health HazardOngoing
DrugMarch 6, 2025· QuVa Pharma, Inc.

Recalled Item: fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.2% ROPivacaine Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 6, 2025· QuVa Pharma, Inc.

Recalled Item: fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.1% Bupivacaine Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 6, 2025· QuVa Pharma, Inc.

Recalled Item: fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.125% Bupivacaine Recalled...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal Coblator II Evac 70 Xtra Plasma Wand Recalled by MEDLINE...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
DrugMarch 5, 2025· Rising Pharma Holding, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Rising Pharma Holding, Inc....

The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2025· Strides Pharma, Inc.

Recalled Item: Testosterone Gel 1% Recalled by Strides Pharma, Inc. Due to Presence of...

The Issue: Presence of foreign substance: Presence of Benzene.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2025· Strides Pharma, Inc.

Recalled Item: Testosterone Gel 1% Recalled by Strides Pharma, Inc. Due to Presence of...

The Issue: Presence of foreign substance: Presence of Benzene.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal ENT Coblator II PROcise XP Wand Recalled by MEDLINE...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
DrugMarch 5, 2025· Golden State Medical Supply Inc.

Recalled Item: PRASUGREL TABLETS Recalled by Golden State Medical Supply Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal Coblator II ENT Evac 70 Xtra HP Recalled by MEDLINE...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
DrugMarch 5, 2025· L'Oreal USA

Recalled Item: La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne...

The Issue: Chemical Contamination: This recall has been initiated due to detected trace...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2025· L'Oreal USA

Recalled Item: La Roche-Posay Laboratoire Dermatologique Effaclar Dermatological Acne...

The Issue: cGMP Deviations: The recall was initiated due to detected trace levels of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2025· L'Oreal USA

Recalled Item: La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne...

The Issue: cGMP Deviations: The recall was initiated due to detected trace levels of...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal ENT Coblator II PROcise mAx Recalled by MEDLINE INDUSTRIES,...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Abbott Diagnostics Scarborough, Inc.

Recalled Item: Brand Name: ID NOW Influenza A/B 2 24T Product Name: Recalled by Abbott...

The Issue: The impacted lots have a higher occurrence of invalid rates when compared to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2025· Medtronic MiniMed, Inc.

Recalled Item: InPen smart insulin pen Recalled by Medtronic MiniMed, Inc. Due to Insulin...

The Issue: Insulin pens may have been incorrectly assembled therefore users could...

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

Class II — Potential Health HazardOngoing