Product Recalls in Nebraska
Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,455 recalls have been distributed to Nebraska in the last 12 months.
Showing 23221–23240 of 49,150 recalls
Recalled Item: Good Neighbor Pharmacy Recalled by Twenty-First Century Healthcare, Inc Due...
The Issue: 21st Century HealthCare, Inc. is recalling Good Neighbor Pharmacy brand Co...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Good Neighbor Pharmacy Recalled by Twenty-First Century Healthcare, Inc Due...
The Issue: 21st Century HealthCare, Inc. is recalling Good Neighbor Pharmacy brand Co...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: COBRA FUSION 150 Ablation System (International Only) Recalled by AtriCure,...
The Issue: There is a potential for patients undergoing ablation to experience an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBRA FUSION 150 Ablation System Recalled by AtriCure, Inc. Due to There is...
The Issue: There is a potential for patients undergoing ablation to experience an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBRA FUSION 150 Ablation System Recalled by AtriCure, Inc. Due to There is...
The Issue: There is a potential for patients undergoing ablation to experience an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBRA FUSION 50 Recalled by AtriCure, Inc. Due to There is a potential for...
The Issue: There is a potential for patients undergoing ablation to experience an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revolution CT scanners Product Usage: The system is intended for head...
The Issue: Additional low dose radiation exposure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alprazolam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...
The Issue: Failed Impurities/Degradation Specifications: Elevated levels of a known...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan and Hydrochlorothiazide Tablets Recalled by Prinston...
The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fexofenadine HCl Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications: Related compound results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan Tablets 300 mg 90 count Rx only Manufactured by: Recalled by...
The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan and Hydrochlorothiazide Tablets Recalled by Prinston...
The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan and Hydrochlorothiazide Tablets Recalled by Prinston...
The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan and HydrochlorothiazideTablets Recalled by Prinston...
The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SKINFUSE Resuce Calming Complex Kit containing: SKINFUSE LIFT HG - Recalled...
The Issue: Cosmetic Kit was packaged with a mislabel medical product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: On-X Aortic Heart Valve with Anatomic Sewing Ring Product Usage: Recalled by...
The Issue: On-X Valve was mislabeled with the incorrect serial number.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NORepinephrine 16 mg added to 0.9% Sodium Chloride (PF) Recalled by KRS...
The Issue: Labeling: Label mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine 4 mg added to 5% Dextrose 250 mL Bag (PF) Recalled by KRS...
The Issue: Labeling: Label mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CHOL+HDL+GLU test strips Recalled by Polymer Technology Systems, Inc. Due to...
The Issue: Some lots of test strips do not fit tightly into the optical block, and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipid Panel test strips (as a component of smart bundles) Recalled by...
The Issue: Some lots of test strips do not fit tightly into the optical block, and may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.