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. 2,768 recalls have been distributed to Indiana in the last 12 months.
Showing 1001–1020 of 13,412 recalls
Recalled Item: Methylphenidate Hydrochloride Recalled by Trigen Laboratories Due to Failed...
The Issue: Failed dissolution specifications: this product is being recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zilretta (triamcinolone acetonide extended-release injectable suspension)...
The Issue: Failed Dissolution Specifications - did not meet the acceptance criteria for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oatmeal Daily Moisturizing Body Lotion (1.3% Dimethicone) Recalled by Brands...
The Issue: Microbial Contamination of Non-Sterile Products: confirmed presence of mold...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: STELLALIFE ADVANCED FORMULA Peppermint Recalled by Homeocare Laboratories,...
The Issue: Microbial Contamination of Non-Sterile Products: presence of Terribacillus...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: STELLALIFE VEGA Oral Care Recalled by Homeocare Laboratories, Inc. Due to...
The Issue: Microbial Contamination of Non-Sterile Products: multiple Bacillus species...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amoxicillin and Clavulanate Potassium Tablets USP Recalled by Teva...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Complete 30C/200C Homeopathic Kit Recalled by Washington Homeopathic...
The Issue: Labeling: Label Mix-up: Some bottles of Ferrum Phosphoricum 200C were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride Extended-Release Capsules Recalled by Glenmark...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefixime for Oral Suspension USP 200 mg/5 mL (50 mL Pack size) Recalled by...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Petroleum Jelly Recalled by Consumer Product Partners, LLC Due to Labeling:...
The Issue: Labeling: Label Mix up; product labeled as pure white petroleum jelly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenazopyridine HCl Tablets USP Recalled by Winder Laboratories, LLC Due to...
The Issue: Product Mix Up. A bottle of Phenazopyridine HCl tablets USP 100 mg contained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Docetaxel Injection Recalled by Sagent Pharmaceuticals Due to Presence of...
The Issue: Presence of Particulate Matter: Presence of particulate matter from the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Asmanex Twisthaler Recalled by Organon Llc Due to Defective Container
The Issue: Defective Container
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Docetaxel Injection Recalled by Sagent Pharmaceuticals Due to Presence of...
The Issue: Presence of Particulate Matter: Presence of particulate matter from the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Asmanex Twisthaler Recalled by Organon Llc Due to Defective Container
The Issue: Defective Container
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Asmanex Twisthaler Recalled by Organon Llc Due to Defective Container
The Issue: Defective Container
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: suntegrity Recalled by SYNCHRONICITY SPA INC, DBA SUNTE Due to CGMP Deviations
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.