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. 2,526 recalls have been distributed to Indiana in the last 12 months.
Showing 34081–34100 of 53,528 recalls
Recalled Item: National Foods Packaging Chicken Base in 25 lb white poly-lined paper bags...
The Issue: Product contains a spice which was tested and found to contain elevated...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: National Foods Packaging Low Sodium Chicken Base in 50 lb Recalled by...
The Issue: Product contains a spice which was tested and found to contain elevated...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Marcaine 0.25% (bupivacaine HCl) injection Recalled by Hospira Inc., A...
The Issue: Lack of Assurance of Sterility and Subpotent Drug: defect in glass vial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Marcaine 0.5% (bupivacaine HCl) injection Recalled by Hospira Inc., A Pfizer...
The Issue: Lack of Assurance of Sterility and Subpotent Drug: defect in glass vial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vascular Solutions Twin-Pass RX Dual Access Catheter Recalled by Vascular...
The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 5ml Syringe Luer-Lok" Tip with Blunt Fill Needle 18G Recalled by Becton...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 3ml Syringe Luer-Lok" Tip Catalog 309657 The BD Single Use Recalled by...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Updated Natus neoBLUE blanket LED Phototherapy Systems. It provides...
The Issue: The firm sent the Technical Bulletin to consignees who received the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascular Solutions Twin-Pass .023" Dual Access Catheter Recalled by Vascular...
The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascular Solutions Twin-Pass Dual Access Catheter Recalled by Vascular...
The Issue: Vascular Solutions is recalling Twin-Pass dual access catheters because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RTI Surgical Streamline OCT Occipito-Cervico-Thoracic Spinal Rod Recalled by...
The Issue: RTI Surgical Inc. (RTI) is conducting a voluntary recall on two specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 18G Recalled by...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD SafetyGlide" Injection Needle Catalog #305917 The SafetyGlide " needle...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 23G Recalled by...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 3ml Syringer Luer-Lok Tip Catalog #309604 The BD Single Use Recalled by...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 10mL Syringe Luer-Lok Tip Catalog number 301997 The BD Single Use...
The Issue: BD identified that several lots did not receive the specified dose of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Keystone Dental PrimaConnex¿ Straight Implant TC Recalled by Keystone Dental...
The Issue: Small diameter (SD) cover screw was packaged with the regular diameter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Chemistry 1 Calibrator The Chemistry 1 Calibrator (KC110B)...
The Issue: Siemens determined that discrepant low calcium recovery of QC and patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fujifilm Synapse PACS Recalled by Fujifilm Medical Systems U.S.A., Inc. Due...
The Issue: Image data for a patients image may not be correct
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRACH'S Chocolate Creations Recalled by Ferrara Candy Comp Due to Undeclared...
The Issue: Undeclared peanuts and wheat in product.
Recommended Action: Do not consume. Return to store for a refund or discard.