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. 2,741 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
2,741 in last 12 months

Showing 61616180 of 13,412 recalls

DrugDecember 17, 2018· Promise Pharmacy, LLC

Recalled Item: Leucine/Isoleucine/Valine injection Recalled by Promise Pharmacy, LLC Due to...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2018· Promise Pharmacy, LLC

Recalled Item: Sermorelin 9 mg injection Recalled by Promise Pharmacy, LLC Due to Lack of...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2018· Promise Pharmacy, LLC

Recalled Item: Glutathione Injection Recalled by Promise Pharmacy, LLC Due to Lack of...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2018· Cipla Limited

Recalled Item: Nevirapine Extended Release Tablets Recalled by Cipla Limited Due to Failed...

The Issue: Failed Dissolution Specifications.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2018· Results RNA, LLC

Recalled Item: Lubrisine eye drops (polyethylene glycol 400 0.4% and Propylene glycol 0.3%)...

The Issue: Lack of Sterility Assurance and Incorrect/Undeclared excipient: Product was...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 10, 2018· Gordon Laboratories

Recalled Item: Monsel's (Ferric Subsulfate) Solution Recalled by Gordon Laboratories Due to...

The Issue: Superpotent Drug: contains higher levels of Iron than labeled.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2018· US Pharmaceuticals Inc.

Recalled Item: Medline Remedy Essential Barrier Skin Protectant Ointment (petrolatum 59%)...

The Issue: GMP Deviations: Out of specification results for Total Aerobic Microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2018· US Pharmaceuticals Inc.

Recalled Item: Soothe & Cool Protect Moisture Guard Skin Protectant (petrolatum 59%)...

The Issue: GMP Deviations: Out of specification results for Total Aerobic Microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 7, 2018· Sun Pharmaceutical Industries, Inc.

Recalled Item: Absorica (Isotretinoin) Capsules 30 mg USP Recalled by Sun Pharmaceutical...

The Issue: Subpotent Drug: Isotretinoin content results were lower than the...

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

Class III — Low RiskOngoing
Refund
DrugDecember 7, 2018· US Pharmaceuticals Inc.

Recalled Item: Hydrocortisone Cream 1% MS Anti itch Cream with Intensive Healing 2 oz tubes...

The Issue: GMP Deviations: Out of specification results for Total Aerobic Microbial...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 6, 2018· Pfizer Inc.

Recalled Item: Levoxyl (levothyroxine sodium tablets Recalled by Pfizer 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
DrugDecember 5, 2018· Pharmedium Services, LLC

Recalled Item: Fentanyl Citrate 2 mcg per mL (200 mcg per 100 Recalled by Pharmedium...

The Issue: Sub-potent

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 5, 2018· Pharmedium Services, LLC

Recalled Item: Fentanyl Citrate 2 mcg per mL (100 mcg per 50 Recalled by Pharmedium...

The Issue: Sub-potent

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2018· Epic Pharma, LLC

Recalled Item: Estradiol Tablets Recalled by Epic Pharma, LLC Due to Presence of foreign...

The Issue: Presence of foreign tablet/capsule: A single foreign tablet was found in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 30, 2018· Aurobindo Pharma USA Inc.

Recalled Item: Amlodipine and Olmesartan Medoxomil Tablets Recalled by Aurobindo Pharma USA...

The Issue: Discoloration: This product is being recalled due to a confirmed pharmacist...

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

Class III — Low RiskOngoing
Refund
DrugNovember 30, 2018· VistaPharm, Inc.

Recalled Item: NYSTATIN Oral Suspension Recalled by VistaPharm, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:Out of specification for...

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

Class III — Low RiskOngoing
Refund
DrugNovember 27, 2018· Teva Pharmaceuticals USA

Recalled Item: Amlodipine and Valsartan Tablets 5 mg/320 mg Recalled by Teva...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 27, 2018· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Aprepitant Capsules Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: Shortfill: Aprepitant capsules 40 mg is being recalled due to customer...

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

Class III — Low RiskOngoing
Refund
DrugNovember 27, 2018· Teva Pharmaceuticals USA

Recalled Item: Amlodipine and Valsartan Tablets 5 mg/160 mg Recalled by Teva...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 27, 2018· Teva Pharmaceuticals USA

Recalled Item: Amlodipine and Valsartan Tablets 10 mg/320 mg (a) 30-count bottles Recalled...

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund