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. 2,535 recalls have been distributed to North Dakota in the last 12 months.
Showing 9241–9260 of 47,938 recalls
Recalled Item: DYNAMITE SUPER capsule Recalled by Gadget Island, Inc Due to Undeclared...
The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pro Power Knight Plus capsule Recalled by Gadget Island, Inc Due to...
The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NUX Male Enhancement capsule Recalled by Gadget Island, Inc Due to...
The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HeartSine Recalled by HeartSine Technologies Ltd Due to Single use battery...
The Issue: Single use battery and electrode cartridge may be rendered inoperable due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziyad cinnamon powder Recalled by ZB Importing LLC Due to Elevated levels of...
The Issue: Elevated levels of lead
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FILMARRAY Gastrointestinal (GI) Panel (Part No.: RFIT-ASY-0104 &...
The Issue: The firm has identified an increased risk of obtaining false positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT for Brazil SKD-Computed Tomography X-Ray System Model: 728146...
The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT-Computed Tomography X-Ray System Model: 728143 Recalled by...
The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT Power (China)-Computed Tomography X-Ray System Model: 728148...
The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Incisive CT Plus-Computed Tomography X-Ray System Model: 728149 Recalled by...
The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventralight ST w Echo PS 4.5" Circle A low profile Recalled by Davol, Inc....
The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventralight ST w EchoPS 4"x6" Ellipse- A low profile Recalled by Davol, Inc....
The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventralight ST 4.5" Circle with Echo PS- A low profile Recalled by Davol,...
The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ventralight ST 4" x 6" Ellipse with Echo PS Catalog Number: 5955460 Recalled...
The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SteriPack Sterile Polyester Spun Swabs (25 units/Pack)- Intended for sample...
The Issue: Fails Post-Sterilization Sterile Swabs Cantilever (Bend) Testing and may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK SymphoKnee System L-Shaped Femoral Augment Recalled by Linkbio Corp....
The Issue: Contains the incorrect implant in the packaging. The packaging incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gabapentin Tablets Recalled by The Harvard Drug Group Due to Product mixup:...
The Issue: Product mixup: one foreign tablet found in product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xpert Xpress Strep A Recalled by Cepheid Due to pipettes packaged in Strep A...
The Issue: pipettes packaged in Strep A test may fail to dispense an adequate sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xpert Xpress Strep A Recalled by Cepheid Due to pipettes packaged in Strep A...
The Issue: pipettes packaged in Strep A test may fail to dispense an adequate sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AVNS ambIT System - PIB/PCA W 2.5in Cath Recalled by Avanos Medical, Inc....
The Issue: Some of the ambIT kits were potentially distributed without an air in-line...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.