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. 1,097 recalls have been distributed to Indiana in the last 12 months.
Showing 15081–15100 of 53,528 recalls
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: 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: 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 and Presence of Foreign Tablets/Capsules;...
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: SuperCore Biopsy Instrument: REF/Product Description: 701114090/SUPERCORE...
The Issue: Due to component (housing and plunger) detaching from the semi-automatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cliquid MD version 3.4 software used in conjunction with Analyst Recalled by...
The Issue: The values of the Internal Standard (IS) concentrations are incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMART FLEX 8x60 BIL Recalled by Cordis Corporation Due to There is a...
The Issue: There is a potential for distal tip dislodgement or separation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMART FLEX 10x100 BIL Recalled by Cordis Corporation Due to There is a...
The Issue: There is a potential for distal tip dislodgement or separation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: .15.010 Recalled by Limacorporate S.p.A Due to There is a potential that the...
The Issue: There is a potential that the length of bone screws identified on labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMART FLEX 9x60 BIL Recalled by Cordis Corporation Due to There is a...
The Issue: There is a potential for distal tip dislodgement or separation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: .15.020 Recalled by Limacorporate S.p.A Due to There is a potential that the...
The Issue: There is a potential that the length of bone screws identified on labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMART FLEX 6x120 BIL Recalled by Cordis Corporation Due to There is a...
The Issue: There is a potential for distal tip dislodgement or separation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMART FLEX 10x100 BIL Recalled by Cordis Corporation Due to There is a...
The Issue: There is a potential for distal tip dislodgement or separation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMART FLEX 6x150 BIL Recalled by Cordis Corporation Due to There is a...
The Issue: There is a potential for distal tip dislodgement or separation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tinactin (Tolnaftate 1%) POWDER SPRAY NET WT 133g (4.6 oz) can Recalled by...
The Issue: Chemical Contamination: presence of benzene
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: 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.