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 3721–3740 of 13,412 recalls
Recalled Item: Coppertone Pure & Simple 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%...
The Issue: Chemical contamination; presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Butalbital Recalled by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals...
The Issue: Labeling: Not Elsewhere Classified: the controlled substance classification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Butalbital Recalled by Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals...
The Issue: Labeling: Not Elsewhere Classified: the controlled substance classification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Natural Dentist Healthy Balance Peppermint Sage Recalled by Revive...
The Issue: Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artesunate for Injection Recalled by AMIVAS (US), LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility: Air filter failed post integrity test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride Extended-Release Tablets Recalled by Strides Pharma Inc....
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glucagon Emergency Kit for Low Blood Sugar Recalled by Eli Lilly & Company...
The Issue: SUBPOTENT DRUG: Vial contained a liquid substance, instead of the expected...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 55/14 (fluticasone propionate 55 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate Testosterone Propionate Recalled by New Vitalis...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14...
The Issue: Subpotent drug: OOS results of Label Claimed Emitted Dose for salmeterol
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Phenylbutyrate Powder Recalled by SigmaPharm Laboratories LLC Due to...
The Issue: Failed Impurities/Degradation Specifications; Out of Specification impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GlipiZIDE Extended-Release Tablets Recalled by American Health Packaging Due...
The Issue: Failed Dissolution Specifications: results were above specification.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate Injection Recalled by Fresenius Kabi USA LLC Due to...
The Issue: Defective container: Cracked vials leading to lack of sterility assurance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valproic Acid Oral Solution Recalled by American Health Packaging Due to...
The Issue: CGMP Deviations: Potential concern with products manufactured using liquid...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Viatris Due to Failed...
The Issue: Failed Impurities/Degradation Specifications; out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rocuronium Bromide Injection 50mg/5 mL Recalled by Piramal Critical Care,...
The Issue: Labeling: Label Lacks Warning or Rx Legend: Finished product did not include...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Tartrate Tablets USP 100 mg Recalled by Aurobindo Pharma USA Inc....
The Issue: Presence of Foreign Substance: Product complaints received for the presence...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.