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. 1,785 recalls have been distributed to North Dakota in the last 12 months.
Showing 28201–28220 of 47,938 recalls
Recalled Item: HFS 1/10.35 Oven Ready Krispy Krunchy Breaded Alaska Pollock Fillets 3.6 oz....
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: American Pride 1/10lb Fully Cooked Gourmet Breaded Pollock Squares 2 oz....
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HLSC 1/10lb Honey Chipotle Salmon Recalled by High Liner Foods Inc. Due to...
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HFS 1/40 Crunchy Breaded Ocean Perch Fillet 2-3oz WIP. Item Number: 19905610...
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sorin Group Aortic Arch Cannula Recalled by Sorin Group USA, Inc. Due to...
The Issue: Identification of excess plastic on the tip of the cannula.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra 3D Revascularization Device It is indicated for used in Recalled by...
The Issue: Penumbra has identified an issue in these four lots involving a raw material...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TetraStem brand Topical Ointment First Aid Antibiotic Recalled by Phillips...
The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: StaphWash+Plus+ Skin Protectant Recalled by Phillips Co. Due to GMP...
The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VenomX Recalled by Phillips Co. Due to GMP Deviations; FDA inspection found...
The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: StingMed Insect bites Skin Protectant. Zinc acetate (.1% by volume) Recalled...
The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tetracycline-ABC Brand Topical ointment First Aid Antibiotic Recalled by...
The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diabecline brand Topical Ointment First Aid Antibiotic Recalled by Phillips...
The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Accu-Chek Connect Diabetes Management App Recalled by Roche Diabetes Care,...
The Issue: Certain iOS and Android App versions contain a program error (bug) in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Connect diabetes management software app Recalled by Roche...
The Issue: Certain iOS and Android App versions contain a program error (bug) in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IQon Spectral CT (Model No. 728332) Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core (Model No. 728321) Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance Big Bore Radiology CT (Model No. 728244) software version...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT (Model No. 728326) Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 (Model No. 728323) Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 (Model No. 728231) Recalled by Philips Medical Systems...
The Issue: It was reported that scanners running certain software versions provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.