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 10811100 of 13,356 recalls

DrugApril 19, 2024· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Amphotericin B Liposome for Injection Recalled by SUN PHARMACEUTICAL...

The Issue: Out of specification for assay

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2024· Nomax Inc

Recalled Item: GloStrips Recalled by Nomax Inc Due to Failed Impurities/Degradation...

The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2024· Nomax Inc

Recalled Item: FUL-GLO Recalled by Nomax Inc Due to Failed Impurities/Degradation...

The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2024· Nomax Inc

Recalled Item: GloStrips Recalled by Nomax Inc Due to Failed Impurities/Degradation...

The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 19, 2024· Nomax Inc

Recalled Item: FUL-GLO Recalled by Nomax Inc Due to Failed Impurities/Degradation...

The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: ALOE GATOR Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: ALOE GATOR Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...

The Issue: Out of Specification for active ingredient. Violative grade of propylene...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· ARG Laboratories, Inc.

Recalled Item: Bull Frog SPF 50 Amphibious Lotion SPF 50 Amphibious Lotion Recalled by ARG...

The Issue: Out of Specification for active ingredient

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 12, 2024· Dercher Enterprises, Inc., DBA Gordon Laboratories

Recalled Item: Gordofilm Wart Remover (salicylic acid 16.7% USP) packaged in 15 cc glass...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 10, 2024· Imprimis NJOF, LLC

Recalled Item: Prednisolone Sodium Phosphate-Moxifloxacin-Bromfenac Sterile Ophthalmic...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 10, 2024· Imprimis NJOF, LLC

Recalled Item: Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL Preservative-Free...

The Issue: Out of specification for assay

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

Class III — Low RiskOngoing
Refund