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. 2,725 recalls have been distributed to Indiana in the last 12 months.
Showing 10341–10360 of 53,528 recalls
Recalled Item: Dermoplast FIRST AID ANTIBACTERIAL SPRAY (Benzethonium chloride 0.2% First...
The Issue: Subpotent Drug: Low assay observed in one of the two active ingredients...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sunflower Lecithin Liquid Packaged in 2 Recalled by Navada Imports Due to...
The Issue: Undeclared peanut allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Organic Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes Recalled...
The Issue: Undeclared peanut allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sunflower Lecithin Powder Packaged in 44 lb. (20 kg.) boxes Recalled by...
The Issue: Undeclared peanut allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Soybean Lecithin Powder Packaged in 44 lb. (20 kg.) boxes Recalled by Navada...
The Issue: Undeclared peanut allergen
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Given Imaging SmartBar Cereal Bar Recalled by Given Imaging Ltd. Due to...
The Issue: Cereal bar may be contaminated with tobacco beetles.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BEAR Implant (Bridge-Enhanced ACL Restoration) Recalled by Miach...
The Issue: The field action was initiated in February of 2023 and was limited to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno systems with a Siemens Healthineers table or Trumpf/MAQUET...
The Issue: If, during the procedure, X-ray has been released and a image has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Habib EndoHPB Bipolar Radiofrequency (RF) Catheter 8F (2.7mm). A...
The Issue: Cease use of the Habib EndoHPB Bipolar RF Catheter with the ERBE VIO3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno systems with a Siemens Healthineers table or a Recalled by...
The Issue: In the event of any unintended table movement, the system may not detect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LATITUDE NXT Remote Patient Management System Recalled by Boston Scientific...
The Issue: Under specific circumstances, the U.S. product registration system did not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOLOC 3DSi CLAW II 4 HOLE Plate Recalled by Wright Medical Technology,...
The Issue: Stryker has identified an issue that impacts two specific lots of CLAW" II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOLOC 3DSi CLAW II 4 HOLE Plate Recalled by Wright Medical Technology,...
The Issue: Stryker has identified an issue that impacts two specific lots of CLAW" II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD-102 NF Recalled by DuPont Nutrition USA, Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Avicel PH- 102 NF Recalled by DuPont Nutrition USA, Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Avicel PH- 101 NF Recalled by DuPont Nutrition USA, Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Avicel PH-200 NF Recalled by DuPont Nutrition USA, Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD Ultra-Fine Insulin Syringe 0.5mL Recalled by Becton Dickinson & Company...
The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insulin Syringes with the BD Micro-Fine IV Needle 0.5ml Recalled by...
The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Ultra-Fine Insulin Syringe 0.5mL Recalled by Becton Dickinson & Company...
The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.