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 84818500 of 13,356 recalls

DrugNovember 2, 2016· Zydus Pharmaceuticals USA Inc

Recalled Item: BuPROPion Hydrochloride Extended-Release Tablets (XL) Recalled by Zydus...

The Issue: Failed Dissolution Specifications; 6 month time point

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

Class III — Low RiskOngoing
Refund
DrugNovember 1, 2016· Teva Pharmaceuticals USA

Recalled Item: Qnasl (beclomethasone dipropionate) Nasal Aerosol 80 Mcg Recalled by Teva...

The Issue: Failed Content Uniformity: Product was out of specification for spray...

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

Class III — Low RiskOngoing
Refund
DrugNovember 1, 2016· Teva Pharmaceuticals USA

Recalled Item: Qnasl (beclomethasone dipropionate) Nasal Aerosol 40 Mcg Recalled by Teva...

The Issue: Failed Content Uniformity: Product was out of specification for spray...

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

Class III — Low RiskOngoing
Refund
DrugNovember 1, 2016· Hospira Inc.

Recalled Item: Fentanyl Citrate Injection Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Complaints of broken tips on the ampules.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2016· Love My Tru Body

Recalled Item: Skinny Bee Diet capsules Recalled by Love My Tru Body Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA: presence of undeclared sibutramine,...

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 28, 2016· Nationwide Laboratories, LLC

Recalled Item: Salsalate Tablets Recalled by Nationwide Laboratories, LLC Due to CGMP...

The Issue: CGMP Deviations: manufactured under practices which may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2016· Nationwide Laboratories, LLC

Recalled Item: Phenazopyridine Hydrochloride Tablets Recalled by Nationwide Laboratories,...

The Issue: CGMP Deviations: manufactured under practices which may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2016· Nationwide Laboratories, LLC

Recalled Item: Phenazopyridine Hydrochloride Tablets Recalled by Nationwide Laboratories,...

The Issue: CGMP Deviations: manufactured under practices which may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2016· Nationwide Laboratories, LLC

Recalled Item: Salsalate Tablets Recalled by Nationwide Laboratories, LLC Due to CGMP...

The Issue: CGMP Deviations: manufactured under practices which may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: KENALOG (Triamcinolone Acetonide) Spray with Spray Tube Topical Aerosol...

The Issue: Failed Stability Specifications: Low Out of Specification results for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 27, 2016· Amerisource Health Services

Recalled Item: Bupropion Hydrochloride Extended-Release Tablets Recalled by Amerisource...

The Issue: Failed Dissolution Specifications: The firm was notified that there was a...

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

Class III — Low RiskOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: URAMIT MB URINARY ANTISEPTIC Capsules Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: Phenazopyridine Hydrochloride Tablets Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: Hyolev MB URINARY ANTISEPTIC Tablets Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: AZUPHEN MB URINARY ANTISEPTIC Capsules Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: UROPHEN MB URINARY ANTISEPTIC Tablets Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: UROLET MB URINARY ANTISEPTIC Recalled by Burel Pharmaceuticals Inc Due to...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: Phenazopyridine Hydrochloride Tablets Recalled by Burel Pharmaceuticals Inc...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 24, 2016· Burel Pharmaceuticals Inc

Recalled Item: Indiomin MB URINARY ANTISEPTIC Recalled by Burel Pharmaceuticals Inc Due to...

The Issue: CGMP Deviations; deficiencies at the manufacturer may result in assay or...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 21, 2016· Akorn Inc

Recalled Item: Sodium Chloride Ophthalmic Solution Recalled by Akorn Inc Due to Subpotent...

The Issue: Subpotent Drug: concentration of product is less than labeled amount.

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

Class II — Potential Health HazardOngoing
Refund