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. 2,580 recalls have been distributed to Nebraska in the last 12 months.
Showing 11621–11640 of 13,356 recalls
Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...
The Issue: Subpotent Drug: Assay results obtained during stability testing for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Liptruzet (ezetimibe and atorvastin) tablets Recalled by Merck & Co Inc Due...
The Issue: This recall of LIPTRUZET is being initiated due to packaging defects. Some...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Liptruzet (ezetimibe and atorvastin) tablets Recalled by Merck & Co Inc Due...
The Issue: This recall of LIPTRUZET is being initiated due to packaging defects. Some...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PRO ArthMax Dietary Supplement tablets Recalled by HUMAN SCIENCE FOUNDATION...
The Issue: Marketed without an Approved NDA/ANDA; FDA analysis found the product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Liptruzet (ezetimibe and atorvastin) tablets Recalled by Merck & Co Inc Due...
The Issue: Defective Container; some of the outer laminate foil pouches allowed in air...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Liptruzet (ezetimibe and atorvastin) tablets Recalled by Merck & Co Inc Due...
The Issue: This recall of LIPTRUZET is being initiated due to packaging defects. Some...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dermamedics Baby's Relief Calm and Repair Cream in 2 oz. Recalled by...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dermamedics Calm and Correct Serum Recalled by Dermamedics, L.L.C. Due to...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dermamedics Post Procedure Cream 1 oz. containers in the Dermamedics...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dermamedics Complexion Repair Topical Rehydrating Emulsion in 50 ml and...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dermamedics Calm & Correct Cream in 2 oz. containers with SKU number DM1020....
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Therametics Complexion Repair Topical Rehydrating Emulsion in 50 ml and...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dermamedics Calm and Correct Cream 2 oz. containers in the Recalled by...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dermamedics Complexion Repair Topical Rehydrating Emulsion which was...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dermamedics Post Procedure Cream Recalled by Dermamedics, L.L.C. Due to...
The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DOBUTamine Injection Recalled by Hospira Inc. Due to Presence of Particulate...
The Issue: Presence of Particulate Matter: Discolored solution due to a chip in the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aminosyn 3.5% M Sulfite-Free Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility; potential leakage from administrative port.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium 2000 USP Heparin Units per 1000 mL (2 Recalled by Hospira...
The Issue: Lack of Assurance of Sterility; potential leakage from administrative port.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: a) Walgreens Lansoprazole Delayed Release Capsules Recalled by Dr. Reddy's...
The Issue: Microbial Contamination of Non-Sterile Products: Out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zithromax (azithromycin for injection) Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Pfizer is recalling certain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.