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. 902 recalls have been distributed to North Dakota in the last 12 months.
Showing 45221–45240 of 47,938 recalls
Recalled Item: Medtronic DBS Lead Kit for Deep Brain Stimulation Recalled by Medtronic...
The Issue: There is a potential for lead damage due to the use of the lead cap provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic DBS Therapy for Dystonia Kit Recalled by Medtronic Neuromodulation...
The Issue: There is a potential for lead damage due to the use of the lead cap provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare LOGIQ S8 (with software revisions R1.1.1 and R1.5.1) Recalled...
The Issue: GE Healthcare has become aware of a potential safety issue due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avex CX Suite Recalled by Ultradent Products, Inc. Due to Orthodontic...
The Issue: Orthodontic brackets distributed was incorrectly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Egyptian Parsley Flakes Recalled by Specialty Commodities, Inc. Due to...
The Issue: Specialty Commodities was notified by a customer that they had found Parsley...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Organic Lemon Grass Tea Bag Cut (TBC) Recalled by Qtrade Teas And Herb Due...
The Issue: QTrade Teas & Herbs is recalling Organic Lemon Grass Tea Bag Cut (TBC)...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CR MD1.0 General Set Recalled by AGFA Corp. Due to The cassettes were...
The Issue: The cassettes were shipped with the wrong IP (image plate) size bar code.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: Ortho-Clinical Diagnostics, Inc. (OCD) determined that extension springs on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Ortho-Clinical...
The Issue: Ortho-Clinical Diagnostics, Inc. (OCD) determined that extension springs on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Spine Polaris 5.5 Button Lock Screw Inserter. Catalog Number Recalled...
The Issue: Increased risk of failure at the driver tip during screw insertion or removal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Ortho-Clinical Diagnostics, Inc. (OCD) determined that extension springs on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smiths Medical Recalled by Smiths Medical ASD, Inc. Due to In rare...
The Issue: In rare instances, the BCI¿ Remote Alarm Cables (BCI¿ Cable) are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heritage Labs Path Study Extra Supplies Kit Recalled by Heritage Labs...
The Issue: The product has a Lithium Heparin contaminant which could adversely affect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rye bread with the following brands: Village Hearth Recalled by Pan -O- Gold...
The Issue: A recall has been initiated by Pan-O-Gold Baking Co. after they were...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Plum A+3 Infusion Pump. List Number 12618. The Plum A+ Recalled by Hospira...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Hyperbaric Infusion Pump. List Number 11005. The Plum Recalled by...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump. List Number 11971. The Plum A+ Recalled by Hospira...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+ Infusion Pump with Hospira MedNet Software. List Number Recalled by...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+3 Infusion Pump with Hospira MedNet Software. List Number Recalled by...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum A+3 Infusion Pump. List Number 12391. The Plum A+ Recalled by Hospira...
The Issue: The fluid shield diaphragm for the Plum A+ Infusion pumps was undersized,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.