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.

49,150 total recalls
2,580 in last 12 months

Showing 1158111600 of 13,356 recalls

DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: SETON PHARMACEUTICALS Fluocinolone Acetonide 0.01% Topical Oil (Body Oil)...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: ROYAL PHARMACEUTICALS Derma-Smoothe/FS fluocinolone acetonide 0.01% (Scalp...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: ROYAL PHARMACEUTICALS Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: DermOtic Oil (fluocinolone acetonide) 0.01% Ear Drops Recalled by Hill...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil (Scalp Oil)...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: ROYAL PHARMACEUTICALS DermOtic Oil fluocinolone acetonide 0.01% (Ear Drops)...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: SETON PHARMACEUTICALS Fluocinolone Acetonide 0.01% Oil EAR DROPS Recalled by...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS fluocinolone acetonide 0.01% Topical Oil (Body Oil) 4 fl....

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· Hill Dermaceuticals, Inc.

Recalled Item: SETON PHARMACEUTICALS Fluocinolone acetonide 0.01% Topical Oil (Scalp Oil)...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 31, 2014· American Health Packaging

Recalled Item: HydrOXYzine HCl Tablets Recalled by American Health Packaging Due to Good...

The Issue: Good Manufacturing Practices Deviations: The product has an active...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 31, 2014· American Health Packaging

Recalled Item: HydrOXYzine HCl Tablets Recalled by American Health Packaging Due to Good...

The Issue: Good Manufacturing Practices Deviations: The product has an active...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2014· Pfizer Inc.

Recalled Item: GREENSTONE BRAND fluconazole for Oral Suspension Recalled by Pfizer Inc. Due...

The Issue: Defective Container: Tamper evident ring failures discovered on some bottles.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2014· Caraco Pharmaceutical Laboratories Ltd.

Recalled Item: Oxcarbazepine Tablets Recalled by Caraco Pharmaceutical Laboratories Ltd....

The Issue: Failed Tablet Specifications: Broken Tablets Present.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 29, 2014· Fougera Pharmaceuticals Inc.

Recalled Item: Triamcinolone Acetonide Cream USP Recalled by Fougera Pharmaceuticals Inc....

The Issue: Labeling: Label Error on Declared Strength: There is a misprint on the end...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 28, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Metformin HCl Extended-Release Tablets Recalled by Caraco Pharmaceutical...

The Issue: Presence of Foreign Tablet; customer complaint of some tablets of Gabapentin...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 28, 2014· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Carisoprodol Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Impurity/degradation Specification

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

Class III — Low RiskOngoing
Refund
DrugJanuary 27, 2014· Lupin Pharmaceuticals Inc.

Recalled Item: Suprax Recalled by Lupin Pharmaceuticals Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Product did not meet...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 27, 2014· Lupin Pharmaceuticals Inc.

Recalled Item: Suprax Recalled by Lupin Pharmaceuticals Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Product did not meet...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Meizitang Strong Version Botanical Slimming Recalled by MyNicNaxs, Inc. Due...

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 24, 2014· MyNicNaxs, Inc.

Recalled Item: Magic Slim capsules Recalled by MyNicNaxs, Inc. Due to Undeclared Active

The Issue: Marketed Without an Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund