Product Recalls in Indiana

Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,752 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,752 in last 12 months

Showing 35813600 of 13,412 recalls

DrugNovember 12, 2021· SterRx, LLC

Recalled Item: dilTIAZem HCl in 5% Dextrose Injection Recalled by SterRx, LLC Due to Lack...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: EPINEPHIrine in 0.9% Sodium Chloride Injection Recalled by SterRx, LLC Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: PHENYLephrine HCl Recalled by SterRx, LLC Due to Lack of Assurance of Sterility

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: EPINEPHIrine in 0.9% Sodium Chloride Injection Recalled by SterRx, LLC Due...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: Morphine Sulfate in 0.9% Sodium Chloride Injection Recalled by SterRx, LLC...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: NOREPINEPHRINE in 5% Dextrose Injection Recalled by SterRx, LLC Due to Lack...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: 12 HR Allergy & Congestion Relief Fexofenadine HCl Recalled by Dr. Reddy's...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Antihistamine & Nasal Decongestant Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Antihistamine & Nasal Decongestant Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Allergy & Congestion Fexofenadine HCl 60 mg & Pseudoephedrine HCl Recalled...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Fexofenadine HCl Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 9, 2021· PAR Sterile Products LLC

Recalled Item: Buprenorphine HCl Recalled by PAR Sterile Products LLC Due to...

The Issue: Crystallization: presence of white, crystalline product agglomeration...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2021· TOLMAR, Inc.

Recalled Item: Clindamycin and Benzoyl Peroxide Gel Recalled by TOLMAR, Inc. Due to...

The Issue: Superpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2021· Medline Industries Inc

Recalled Item: Hand Sanitizer Foam (ethyl alcohol) Recalled by Medline Industries Inc Due...

The Issue: Defective Container: Customer complaints for leaking bottles and dispensing...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 4, 2021· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Flocinolone Acetonide 0.01% Topical Oil Recalled by Amneal Pharmaceuticals...

The Issue: Subpotent Drug: Out-of-specification assay result was obtained for...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 4, 2021· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Flocinolone Acetonide 0.01% Topical Oil Recalled by Amneal Pharmaceuticals...

The Issue: Subpotent Drug: Out-of-specification assay result was obtained for...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 3, 2021· Ascend Laboratories LLC

Recalled Item: Cefixime Capsules 400 mg Recalled by Ascend Laboratories LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2021· Precision Dose Inc.

Recalled Item: Acetaminophen Oral Suspension Recalled by Precision Dose Inc. Due to cGMP...

The Issue: cGMP Deviations: Product manufactured with contaminated raw ingredient.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 1, 2021· Precision Dose Inc.

Recalled Item: Acetaminophen Oral Suspension Recalled by Precision Dose Inc. Due to cGMP...

The Issue: cGMP Deviations: Product manufactured with contaminated raw ingredient.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2021· Teva Pharmaceuticals USA

Recalled Item: Clonidine Transdermal System Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund