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.
Showing 3681–3700 of 13,412 recalls
Recalled Item: Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL) Recalled by...
The Issue: CGMP Deviations: Lots recalled because they were manufactured at the same...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
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.
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.
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.
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.
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.
Recalled Item: Cetirizine hydrochloride Recalled by A-S Medication Solutions LLC. Due to...
The Issue: Labeling: Not Elsewhere classified: Product was relabeled as 90 tablet count...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.