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. 2,624 recalls have been distributed to Nebraska in the last 12 months.
Showing 6161–6180 of 13,356 recalls
Recalled Item: Quetiapine Tablets USP 400 mg Recalled by Ascend Laboratories LLC Due to...
The Issue: Presence of Foreign Substance; metal shard found in tablet
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medi-Stat Foam Recalled by Ecolab Inc Due to Labeling: Label mix-up - the...
The Issue: Labeling: Label mix-up - the label on the product may not match the formula...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals) Recalled by AMERICAN...
The Issue: Cross contamination with other products: This sub-recall is being initiated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Equi-Soft Foam Recalled by Ecolab Inc Due to Labeling: Label mix-up - the...
The Issue: Labeling: Label mix-up - the label on the product may not match the formula...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clopidogrel Tablets Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed Dissolution Specification: Out-of-Specification results were observed...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Antacid Tablets Recalled by L. Perrigo Company Due to Presence of foreign...
The Issue: Presence of foreign substance: Product found to contain metal particles.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Megestrol Acetate Oral Suspension Recalled by Breckenridge Pharmaceutical,...
The Issue: Failed Stability Specifications: Out-of-Specification results obtained for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: puriton EYE RELIEF DROPS Recalled by Kadesh International Due to...
The Issue: Non-Sterility: Product manufactured under non-sterile production conditions.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Curaplex Epi Safe Kit Recalled by Bound Tree Medical, LLC Due to Labeling...
The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nitrofurantoin Capsules Recalled by Sandoz Inc Due to Cross Contamination...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nitrofurantoin Capsules Recalled by Sandoz Inc Due to Cross Contamination...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isosorbide Dinitrate Tablets Recalled by Sandoz Inc Due to Cross...
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: curaplex Epi Safe Kit Recalled by Bound Tree Medical, LLC Due to Labeling...
The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: curaplex Epi Safe Administration and Training Kits Recalled by Bound Tree...
The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Curaplex Epi Kit NOT FOR IV USE Recalled by Bound Tree Medical, LLC Due to...
The Issue: Labeling Incorrect Instructions: This recall has been initiated because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Curaplex Epi Safe Kit Recalled by Bound Tree Medical, LLC Due to Labeling:...
The Issue: Labeling: Incorrect or missing Lot and/or Exp Date:The Kit is incorrectly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: curaplex Epi Safe Administration and Training Kits # 8600-01100. Kit...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp date: vials of epinephrine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.