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. 2,560 recalls have been distributed to Indiana in the last 12 months.
Showing 23301–23320 of 53,528 recalls
Recalled Item: Articaine DENTAL Recalled by Septodont Inc. Due to Mislabeling
The Issue: Labeling: Not Elsewhere Classified. This recall has been initiated due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DrKids Children's Pain & Fever Oral Solution Acetaminophen 160 mg/5 mL...
The Issue: CGMP Deviations: Recall as a precautionary measure due to potential risk of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CVS Health Children's Cough & Chest Congestion DM Dextromethorphan HBr...
The Issue: CGMP Deviations: Recall as a precautionary measure due to potential risk of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CVS Health Children's Pain & Fever Acetaminophen 160 mg/5 mL Recalled by...
The Issue: CGMP Deviations: Recall as a precautionary measure due to potential risk of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DrKids Children's Allergy Relief Diphenhydramine HCl 12.5 mg/5 mL...
The Issue: CGMP Deviations: Recall as a precautionary measure due to potential risk of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Abbott MitraClip XTR Clip Delivery System Recalled by Abbott Vascular Due to...
The Issue: Reports of implantable mitral valve repair system clips unexpectedly opening...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic 0-arm TM 1000 Imaging Systems: Bl-700-00027-XXX and...
The Issue: The 0-arm 1000 Imaging System uses energy from the batteries to generate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dragonfly Dehydrate Guava Ing: Guava Recalled by U.S. Tov, Inc. Due to...
The Issue: Undeclared sulfites.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ARCHITECT C System Mixer - Product Usage: The ARCHITECT Clinical Recalled by...
The Issue: Mixer blade may separate from mixer due to the screw and nut failure and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Losartan Potassium Tab. USP 50mg Recalled by Preferred Pharmaceuticals, Inc...
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Injection Recalled by Sagent Pharmaceuticals Inc Due...
The Issue: Lack of Sterility Assurance: Microbial growth detected during a routine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mycophenolate Mofetil for Injection Recalled by Par Pharmaceutical, Inc. Due...
The Issue: Presence of Particulate Matter; glass fragment observed in one vial of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject" 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Hook/Triangle Blade Kit Recalled by Stryker GmbH Due to The...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.