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. 1,672 recalls have been distributed to North Dakota in the last 12 months.
Showing 42461–42480 of 47,938 recalls
Recalled Item: enGen Track System with enGen Select v5.0 with autoverification enabled...
The Issue: Ortho Clinical Diagnostics issued an Urgent Product Correction Notification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: enGen Track System with enGen Custom v3.2.2 (& below) Product The VITROS 5...
The Issue: Ortho Clinical Diagnostics issued an Urgent Product Correction Notification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi Parameter Patient Monitor (with Arrhythmia Detection and Alarms)...
The Issue: Mindray has identified an issue with V Series Monitor where the V Dock power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GENESIS(R) II Recalled by Smith & Nephew Inc Due to Swapped product....
The Issue: Swapped product. Non-porous tibial base size 5 L was mis-packaged as size 6...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Plus" 10mm x 12mm Webless implants Pioneer Surgical's C-Plus " Recalled by...
The Issue: As the result of a recent internal review of regulatory documents, we have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Resolute Integrity Zotarolimus-eluting Coronary Stent: Stent ID 3.0 mm...
The Issue: A small number of units in lot number 0006573585 of the Resolute Integrity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: User Defined Method Flex Assignment/Siemens Dimension Vista 500 or Dimension...
The Issue: When utilizing the Routine Inventory screen to enter a User Defined Method...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GENESIS(R) II Recalled by Smith & Nephew Inc Due to Swapped product....
The Issue: Swapped product. Non-porous tibial base size 5 L was mis-packaged as size 6...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slim Expert softgel capsules Dietary Supplement. One month supply/ 30...
The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Slim Fortune capsules Dietary Supplement. Each bottle contains 30 capsules....
The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidiy capsules Dietary Supplement. Each bottle contains 30 capsules....
The Issue: Marketed Without an Approved NDA/ANDA; product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dexedrine¿ (Dextroamphetamine Sulfate) Spansules¿ Sustained Release Capsules...
The Issue: Failed Dissolution Specifications: Out of Specification (OOS) test results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 1) The HomeChoice automated peritoneal dialysis system. Dataplate located on...
The Issue: In systems with version 10.4 software Initial Drain logic, the device will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products COCM Reagent Recalled by Ortho-Clinical...
The Issue: Inaccurate quality control results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Digestive Health Recalled by Ultra Laboratories Due to Ultra Laboratories is...
The Issue: Ultra Laboratories is recalling Digestive Health because a raw material used...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Market Pantry brand Animal Cookies Recalled by D. F. Stauffer Biscuit Co,...
The Issue: undeclared milk and egg in Market Pantry brand white fudge coated Animal Cookies
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: XYLANASE 150 Recalled by Specialty Enzymes & Biotechnologies Due to...
The Issue: Specialty Enzymes and Biotechnologies is recalling cellulase/mannanase and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cellulase: ACTA 4-702 APEX 17-6262 APEX 6-9762 ARTH EB 10831 Recalled by...
The Issue: Specialty Enzymes and Biotechnologies is recalling cellulase/mannanase and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cellulase & Protease: APEX 10-639 A DIGESEB DIGESEB PLUS DIGESEB Recalled by...
The Issue: Specialty Enzymes and Biotechnologies is recalling cellulase/mannanase and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Papain: NF 4-608 B NF 4-6152 NUTRA 6-452 PAPAIN PROHYDROXY NF 4-714 Recalled...
The Issue: Specialty Enzymes and Biotechnologies is recalling cellulase/mannanase and...
Recommended Action: Do not consume. Return to store for a refund or discard.