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. 1,836 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
1,836 in last 12 months

Showing 1686116880 of 47,938 recalls

Medical DeviceOctober 23, 2020· Medtronic Heart Valves Division

Recalled Item: Evolut (TM) PRO+ System. With the following model numbers: a. Recalled by...

The Issue: Potential for Transcatheter Aortic Valve (TAV) leaflet damage when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2020· Medtronic Heart Valves Division

Recalled Item: Evolut (TM) R System. With the following model numbers: a. EVOLUTR-23...

The Issue: Potential for Transcatheter Aortic Valve (TAV) leaflet damage when...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2020· Biomeme, Inc.

Recalled Item: The Biomeme SARS-CoV-2 Real-Time RT-PCR Test is a molecular in Recalled by...

The Issue: The firm has become aware of nine reports by a single customer that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2020· Becton Dickinson & Company

Recalled Item: BD Ultra-Fine Pen Needles 32G x 4mm (5/32' )-intended for Recalled by Becton...

The Issue: Product shelf cartons incorrectly labeled as products intended for the Latin...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2020· Intuitive Surgical, Inc.

Recalled Item: Box Label: ION Fully Articulating Catheter Recalled by Intuitive Surgical,...

The Issue: The distal tip ring of the fully articulating catheter may become dislodged...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2020· Coloplast Manufacturing US, LLC

Recalled Item: Titan Pump - Product Usage: indicated for male patients suffering Recalled...

The Issue: Potential increased occurrence of pump fracture over the lifetime of the device.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 23, 2020· Mako Surgical Corporation

Recalled Item: Mako Integrated Cutting System (MICS) Handpiece Recalled by Mako Surgical...

The Issue: Stryker has discovered a characterization issue associated with the Mako...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2020· Cook Inc.

Recalled Item: Fixed Core Wire Guide Recalled by Cook Inc. Due to Affected product was...

The Issue: Affected product was dropped during manufacturing, which may result in a...

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

Class I — Serious Health HazardOngoing
DrugOctober 21, 2020· H & H Remedies, LLC

Recalled Item: Vapor Ointment packaged in a) 1/8 oz Recalled by H & H Remedies, LLC Due to...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 21, 2020· H & H Remedies, LLC

Recalled Item: White Liniment packaged in a) 1 oz Recalled by H & H Remedies, LLC Due to...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 21, 2020· H & H Remedies, LLC

Recalled Item: Union (black) salve packaged in a) 1/8 oz Recalled by H & H Remedies, LLC...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 21, 2020· JMH International, LLC

Recalled Item: Chef Myron's Szechuan Sauce Recalled by JMH International, LLC Due to...

The Issue: Product utilized a gluten-free claim but has as an ingredient a fermented...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodOctober 21, 2020· JMH International, LLC

Recalled Item: Chef Myron's Tangy Teriyaki Sauce Recalled by JMH International, LLC Due to...

The Issue: Product utilized a gluten-free claim but has as an ingredient a fermented...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodOctober 21, 2020· JMH International, LLC

Recalled Item: Chef Myron's Premium Teriyaki Sauce Recalled by JMH International, LLC Due...

The Issue: Product utilized a gluten-free claim but has as an ingredient a fermented...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodOctober 21, 2020· JMH International, LLC

Recalled Item: Chef Myron's Yakitori Sauce Recalled by JMH International, LLC Due to...

The Issue: Product utilized a gluten-free claim but has as an ingredient a fermented...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodOctober 21, 2020· JMH International, LLC

Recalled Item: Chef Myron's Premium Shoyu Sauce Recalled by JMH International, LLC Due to...

The Issue: Product utilized a gluten-free claim but has as an ingredient a fermented...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodOctober 21, 2020· JMH International, LLC

Recalled Item: Chef Myron's Ponzu Sauce Recalled by JMH International, LLC Due to Product...

The Issue: Product utilized a gluten-free claim but has as an ingredient a fermented...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodOctober 21, 2020· JMH International, LLC

Recalled Item: Chef Myron's Eurasian Fusion Sauce Recalled by JMH International, LLC Due to...

The Issue: Product utilized a gluten-free claim but has as an ingredient a fermented...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodOctober 21, 2020· JMH International, LLC

Recalled Item: Chef Myron's Tsukeyaki Sauce Recalled by JMH International, LLC Due to...

The Issue: Product utilized a gluten-free claim but has as an ingredient a fermented...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 21, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee floor Recalled by Siemens Medical Solutions USA, Inc Due to Some...

The Issue: Some electronic components within the generator were equipped with an...

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

Class II — Potential Health HazardOngoing