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. 2,650 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
2,650 in last 12 months

Showing 961980 of 13,356 recalls

DrugJuly 10, 2024· Endo Pharmaceuticals, Inc.

Recalled Item: Clonazepam Orally Disintegrating Tablets Recalled by Endo Pharmaceuticals,...

The Issue: Labeling: Label Error on Declared Strength; Some cartons were incorrectly...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 9, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Nitrofurantoin Capsules Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 3, 2024· TAILSTORM HEALTH INC

Recalled Item: Lidocaine HCL Injection Recalled by TAILSTORM HEALTH INC Due to Subpotent...

The Issue: Subpotent Drug: reduced efficacy for epinephrine

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2024· Novel Laboratories, Inc. d.b.a Lupin Somerset

Recalled Item: PEG-3350 Recalled by Novel Laboratories, Inc. d.b.a Lupin Somerset Due to...

The Issue: Defective container: potential for non-sealed pouches which can lead to...

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

Class III — Low RiskOngoing
Refund
DrugJuly 2, 2024· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Verapamil Hydrochloride Injection Recalled by Zydus Pharmaceuticals (USA)...

The Issue: Cross contamination with other products.

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

Class III — Low RiskOngoing
Refund
DrugJuly 2, 2024· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Verapamil Hydrochloride Injection Recalled by Zydus Pharmaceuticals (USA)...

The Issue: Cross contamination with other products.

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

Class III — Low RiskOngoing
Refund
DrugJuly 2, 2024· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Micafungin for injection Recalled by Zydus Pharmaceuticals (USA) Inc Due to...

The Issue: Cross contamination with other products

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

Class III — Low RiskOngoing
Refund
DrugJuly 2, 2024· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Micafungin for injection Recalled by Zydus Pharmaceuticals (USA) Inc Due to...

The Issue: Cross contamination with other products

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

Class III — Low RiskOngoing
Refund
DrugJuly 2, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Decitabine for Injection 50mg per vial Recalled by SUN PHARMACEUTICAL...

The Issue: CGMP Deviations: Out of Specification for Total Aerobic Microbial Count...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 28, 2024· Teva Pharmaceuticals USA, Inc

Recalled Item: Fludrocortisone Acetate Tablets Recalled by Teva Pharmaceuticals USA, Inc...

The Issue: Failed Impurities/Degradation Specifications: Product is being recalled due...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 28, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Pravastatin Sodium Tablets Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: Failed Dissolution Specifications: results below specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2024· Guru Inc.

Recalled Item: Infla-650 Herbal Dietary Supplement Recalled by Guru Inc. Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA: FDA analysis found product to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Sevelamer Carbonate for Oral Suspension 0.8g packets Recalled by Dr. Reddy's...

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

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

Class III — Low RiskOngoing
Refund
DrugJune 26, 2024· RemedyRepack Inc.

Recalled Item: Potassium Chloride Micro 10mEq K (750 mg) Extended Release Capsules Recalled...

The Issue: CGMP Deviations: Out of specification for dissolution

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2024· Equibal Inc

Recalled Item: Blemfree All Day Lotion (salicylic acid 0.5% w/w) Recalled by Equibal Inc...

The Issue: CGMP Deviations: Manufactured without following Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2024· Medisca Inc.

Recalled Item: Budesonide Recalled by Medisca Inc. Due to CGMP Deviations and Presence of...

The Issue: CGMP Deviations and Presence of Particulate Matter: Glass

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2024· Amerisource Health Services LLC

Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Amerisource Health...

The Issue: Failed Dissolution Specifications

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 25, 2024· GLOBAL WIDGET LLC

Recalled Item: Hemp Bombs CBD Pain Freeze (menthol 4%) Recalled by GLOBAL WIDGET LLC Due to...

The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...

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

Class III — Low RiskOngoing
Refund
DrugJune 25, 2024· GLOBAL WIDGET LLC

Recalled Item: Nature's Script CBD Cryotherapy Pain Relief Roll on (menthol 4%) 200mg...

The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...

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

Class III — Low RiskOngoing
Refund
DrugJune 25, 2024· GLOBAL WIDGET LLC

Recalled Item: Hemp Bombs CBD Pain Freeze (menthol 4%) Recalled by GLOBAL WIDGET LLC Due to...

The Issue: Subpotent drug: The potency of the active (menthol) was less than the label...

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

Class III — Low RiskOngoing
Refund