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. 2,503 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,503 in last 12 months

Showing 1194111960 of 47,938 recalls

DrugMay 18, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: Ketamine Hydrochloride Injection Recalled by Nephron Sterile Compounding...

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
DrugMay 18, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Nephron Sterile Compounding...

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
DrugMay 18, 2022· Strides Pharma Inc.

Recalled Item: Losartan Potassium Tablets Recalled by Strides Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 18, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: Lidocaine HCl Injection Recalled by Nephron Sterile Compounding Center LLC...

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
DrugMay 17, 2022· Family Dollar Stores, Llc.

Recalled Item: Only At Family Dollar AMBI Skincare Even & Clear Nourishing Recalled by...

The Issue: cGMP deviations: product stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 17, 2022· Family Dollar Stores, Llc.

Recalled Item: Luxury Hygiene Hand Sanitizer Moisturizing Formula with Vitamin E Recalled...

The Issue: cGMP deviations: product stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 17, 2022· Family Dollar Stores, Llc.

Recalled Item: AMBI Skincare Fade Cream Oily Skin New & Improved Recalled by Family Dollar...

The Issue: cGMP deviations: product stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 17, 2022· Family Dollar Stores, Llc.

Recalled Item: Aveeno Daily Moisturizing lotion Fragrance Free with Soothing Oat & Recalled...

The Issue: cGMP deviations: product stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 17, 2022· Family Dollar Stores, Llc.

Recalled Item: AMBI Skincare Fade Cream Normal Skin Recalled by Family Dollar Stores, Llc....

The Issue: cGMP deviations: product stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 17, 2022· Family Dollar Stores, Llc.

Recalled Item: Luxury Hygiene Hand Sanitizer Moisturizing Formula with Vitamin E Advanced...

The Issue: cGMP deviations: product stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 17, 2022· Family Dollar Stores, Llc.

Recalled Item: AMBI Skincare Even & Clear Exfoliating Wash Salicylic Acid Acne Recalled by...

The Issue: cGMP deviations: product stored outside of labeled temperature requirements.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 17, 2022· Baxter Healthcare Corporation

Recalled Item: #1 MAC F/O LARYNGOSCOPE Recalled by Baxter Healthcare Corporation Due to...

The Issue: Packaging error.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2022· Draeger Medical, Inc.

Recalled Item: Drager SafeStar 55 Recalled by Draeger Medical, Inc. Due to Possible...

The Issue: Possible occlusion of filters due to manufacturing error.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 13, 2022· Rayner Intraocular Lenses Ltd

Recalled Item: RayOne Preloaded Hydrophilic Acrylic IOL Injection Systems containing one...

The Issue: The outer package is mislabeled and the package contains a different IOL...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2022· Volcano Corp

Recalled Item: Volcano Visions PV. 035 Digital IVUS Catheter Recalled by Volcano Corp Due...

The Issue: Digital IVUS catheter instructions for use ( IFU) do not contain...

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

Class III — Low RiskOngoing
Medical DeviceMay 13, 2022· Covidien, LP

Recalled Item: EEA Autosuture Circular Stapler with DST Series Technology Recalled by...

The Issue: The affected staplers have the potential for the staple guide to not be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2022· Volcano Corp

Recalled Item: Volcano Visions PV. 035 Digital IVUS Catheter Recalled by Volcano Corp Due...

The Issue: Digital IVUS catheter instructions for use ( IFU) do not contain...

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

Class III — Low RiskOngoing
DrugMay 13, 2022· Washington Homeopathic Products, Inc.

Recalled Item: Colibacillinum Recalled by Washington Homeopathic Products, Inc. Due to cGMP...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2022· Washington Homeopathic Products, Inc.

Recalled Item: Tuberculinum Bovinum Recalled by Washington Homeopathic Products, Inc. Due...

The Issue: cGMP deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 13, 2022· GlaxoSmithKline LLC

Recalled Item: Tivicay (dolutegravir) Tablets 50 mg Recalled by GlaxoSmithKline LLC Due to...

The Issue: Labeling: incorrect or missing lot and/or expiration date. An incorrect...

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

Class III — Low RiskOngoing
Refund