Product Recalls in Arkansas

Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,645 recalls have been distributed to Arkansas in the last 12 months.

49,990 total recalls
2,645 in last 12 months

Showing 36813700 of 13,434 recalls

DrugOctober 12, 2021· Lupin Pharmaceuticals Inc.

Recalled Item: Irbesartan Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 12, 2021· Lupin Pharmaceuticals Inc.

Recalled Item: Irbesartan Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 12, 2021· Lupin Pharmaceuticals Inc.

Recalled Item: Irbesartan and Hydrochlorothiazide Tablets USP Recalled by Lupin...

The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 8, 2021· Lupin Pharmaceuticals Inc.

Recalled Item: Imipramine Pamoate Capsules 125 mg Recalled by Lupin Pharmaceuticals Inc....

The Issue: Out of specification result observed in a dissolution test at the 9-month...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled by Dr. Reddy's...

The Issue: Failed Excipient Specifications; product manufactured using an excipient...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled by Dr. Reddy's...

The Issue: Failed Excipient Specifications and Presence of Foreign Tablets/Capsules;...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled by Dr. Reddy's...

The Issue: Failed Excipient Specifications; product manufactured using an excipient...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Omeprazole Delayed-Release Capsules Recalled by Dr. Reddy's Laboratories,...

The Issue: CGMP Deviations: Customer complaint for the presence of a staple co-mingled...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled by Dr. Reddy's...

The Issue: Failed Excipient Specifications; product manufactured using an excipient...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 5, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets Recalled by Dr. Reddy's...

The Issue: Failed Excipient Specifications; product manufactured using an excipient...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 4, 2021· Akorn, Inc.

Recalled Item: Betaxolol Ophthalmic Solution Recalled by Akorn, Inc. Due to Microbial...

The Issue: Microbial Contamination of Sterile Products: Confirmed sterility failure...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 1, 2021· Bayer Healthcare Pharmaceuticals Inc.

Recalled Item: Tinactin (Tolnaftate 1%) LIQUID SPRAY NET WT150g (5.3 OZ) can Recalled by...

The Issue: Chemical Contamination: presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 1, 2021· Bayer Healthcare Pharmaceuticals Inc.

Recalled Item: Tinactin (Tolnaftate 1%) DEODORANT POWDER SPRAY NET WT 133g (4.6 OZ) can...

The Issue: cGMP Deviations: manufactured at the same facility where other lots were...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 1, 2021· Bayer Healthcare Pharmaceuticals Inc.

Recalled Item: LOTRIMIN AF Recalled by Bayer Healthcare Pharmaceuticals Inc. Due to...

The Issue: Chemical Contamination: presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 1, 2021· Bayer Healthcare Pharmaceuticals Inc.

Recalled Item: LOTRIMIN AF (Miconazole nitrate 2%) Deodorant Powder Spray NET WT Recalled...

The Issue: cGMP Deviations: manufactured at the same facility where other lots were...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 1, 2021· Bayer Healthcare Pharmaceuticals Inc.

Recalled Item: Lotrimin AF (Tolnaftate 1%) Daily Prevention deodorant powder spray Recalled...

The Issue: Chemical Contamination: presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 1, 2021· Bayer Healthcare Pharmaceuticals Inc.

Recalled Item: LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray NET...

The Issue: cGMP Deviations: manufactured at the same facility where other lots were...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 1, 2021· Bayer Healthcare Pharmaceuticals Inc.

Recalled Item: LOTRIMIN AF (Miconazole nitrate 2%) Deodorant Powder Spray Recalled by Bayer...

The Issue: Chemical Contamination: presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 1, 2021· Bayer Healthcare Pharmaceuticals Inc.

Recalled Item: LOTRIMIN AF (Tolnaftate 1%) DAILY PREVENTION deodorant powder spray Recalled...

The Issue: cGMP Deviations: manufactured at the same facility where other lots were...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 1, 2021· Bayer Healthcare Pharmaceuticals Inc.

Recalled Item: Tinactin (Tolnaftate 1%) DEODORANT POWDER SPRAY NET WT 133g (4.6 OZ) can...

The Issue: Chemical Contamination: presence of benzene

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

Class I — Serious Health HazardOngoing
Refund