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. 2,612 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,612 in last 12 months

Showing 74817500 of 13,356 recalls

DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Bi-Est (Estriol/Estradiol) (80/20) + Progesterone 7.5 mg/200 mg Cream...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 16, 2017· KRS Global Biotechnology, Inc

Recalled Item: Hydroquinone 8%/ Tretinoin 0.1% Topical Ointment packaged in jars Recalled...

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: Beyond Use Date (BUD)...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2017· Renaissance Lakewood, LLC

Recalled Item: Fluconazole Injection Recalled by Renaissance Lakewood, LLC Due to Superpotent

The Issue: Superpotent

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 10, 2017· Baxter Healthcare Corporation

Recalled Item: Nexterone (amiodarone HCl) Premixed Injection Recalled by Baxter Healthcare...

The Issue: Presence of Particulate Matter:Particulate identified as polyethylene, the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 9, 2017· Teva Pharmaceuticals USA

Recalled Item: Clozapine Tablets USP Recalled by Teva Pharmaceuticals USA Due to Failed...

The Issue: Failed Tablet/Capsule Specifications; potential presence of broken tablets.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 9, 2017· Kareway Products Inc

Recalled Item: GERICARE Eyewash Recalled by Kareway Products Inc Due to Non-sterility:...

The Issue: Non-sterility: confirmed microbial contamination with Achromobacter xylosoxidans

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 9, 2017· Mayne Pharma Inc

Recalled Item: Liothyronine Sodium Tablets Recalled by Mayne Pharma Inc Due to Failed...

The Issue: Failed Dissolution Specifications.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2017· L. Perrigo Company

Recalled Item: Maximum Strength Zephrex-D Recalled by L. Perrigo Company Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2017· West-Ward Pharmaceuticals Corp.

Recalled Item: Dexamethasone Sodium Phosphate Injection Recalled by West-Ward...

The Issue: Failed Impurities/Degradation Specifications: high out of specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 6, 2017· West-Ward Pharmaceuticals Corp.

Recalled Item: Dexamethasone Sodium Phosphate Injection Recalled by West-Ward...

The Issue: Failed Impurities/Degradation Specifications: high out of specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 6, 2017· Claris Lifesciences Inc

Recalled Item: Ciprofloxacin in Dextrose (5%) Injection Recalled by Claris Lifesciences Inc...

The Issue: Superpotent

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugNovember 3, 2017· Mylan Pharmaceuticals Inc.

Recalled Item: bupPROPion HCL Extended-Release Tablets Recalled by Mylan Pharmaceuticals...

The Issue: Failed Impurities/Degradation Specifications: Mylan Pharmaceuticals Inc. is...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 30, 2017· Pharmedium Services, LLC

Recalled Item: ePHEDrine Sulfate In 0.9% Sodium Chloride Recalled by Pharmedium Services,...

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 30, 2017· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Meclizine hydrochloride tablets USP Recalled by Jubilant Cadista...

The Issue: Marketed without an approved NDA/ANDA: Bottles were released prior to final...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 30, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol Recalled by Dr....

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date; lot number on the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugOctober 27, 2017· Fresenius Kabi USA, LLC

Recalled Item: Midazolam Injection Recalled by Fresenius Kabi USA, LLC Due to Labeling:...

The Issue: Labeling: Label MIX-UP. Blister Packages, Labeled as Midazolam injection,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugOctober 25, 2017· Teva Pharmaceuticals USA

Recalled Item: Dutasteride and Tamsulosin HCl Capsules Recalled by Teva Pharmaceuticals USA...

The Issue: Failed dissolution specifications; all lots within expiry are being recalled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 25, 2017· Fagron, Inc

Recalled Item: Estriol Recalled by Fagron, Inc Due to cGMP Deviations: lack of quality...

The Issue: cGMP Deviations: lack of quality assurance at the API manufacturer.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2017· Amerisource Health Services

Recalled Item: Paroxetine Tablets Recalled by Amerisource Health Services Due to Presence...

The Issue: Presence of Foreign Tablets/Capsules.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugOctober 20, 2017· Pfizer Inc.

Recalled Item: diphenoxylate hydrochloride and atropine sulfate tablets Recalled by Pfizer...

The Issue: SUPERPOTENT: Weight variations resulting in tablets that are sub and super...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund