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 1261–1280 of 53,528 recalls
Recalled Item: Model: CT 5300 Recalled by PHILIPS MEDICAL SYSTEMS Due to Issue 1: The...
The Issue: Issue 1: The potential for unintentional continued gantry/couch movement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model: Incisive CT Recalled by PHILIPS MEDICAL SYSTEMS Due to Issue 1: The...
The Issue: Issue 1: The potential for unintentional continued gantry/couch movement...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOW Real Food Organic Unsalted Whole Raw Cashews Recalled by Now Foods Due...
The Issue: Undeclared pine nut
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Entecavir Tablets Recalled by Zydus Pharmaceuticals (USA) Inc Due to Failed...
The Issue: Failed impurity/degradation specifications:Out of Specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Entecavir Tablets Recalled by Zydus Pharmaceuticals (USA) Inc Due to Failed...
The Issue: Failed impurity/degradation specifications:Out of Specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HARMONIC FOCUS Shears + Adaptive Tissue Technology Recalled by Stryker...
The Issue: Due to manufacturing issue, reprocessed shears, may become stuck in the "on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Aesculap Product Name: SEALING UNIT F/10/12MM TROCARS W.REDUCER...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AESCULAP Product Name: REDUCING CONVERTER 10/12MM TO 5MM...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Aesculap Product Name: SEALING CAP FOR 10/12MM TROCARS Recalled...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AESCULAP Product Name: SEALING UNIT FOR 10/12MM TROCARS Recalled...
The Issue: It was determined there is the potential of silicone fragments detaching...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OptiWize Health OptiWize Collagen Plus 320 count bottle Recalled by Optiwize...
The Issue: The firm initiated a voluntary recall after NSF testing showed that labeled...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sting Relief Swabs Recalled by ACME UNITED CORPORATION Due to Product Mix-up
The Issue: Product Mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Klassic BiPolar Head Model/Catalog Number: 3205.41.022 Klassic...
The Issue: Potential packaging issue that could compromise the sterile barrier. Defect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor Connect Software Recalled by Becton Dickinson & Co. Due to...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD EpiCenter Microbiology Data Management System Recalled by Becton...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC Blood Culture System Recalled by Becton Dickinson & Co. Due to...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC Blood Culture System Recalled by Becton Dickinson & Co. Due to...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MAX System Recalled by Becton Dickinson & Co. Due to Product service...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix M50 Instrument Recalled by Becton Dickinson & Co. Due to Product...
The Issue: Product service credentials used by some BD technical support teams to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bevacizumab 1.75 mg/0.07 mL - 0.25 mL syringe Recalled by RC Outsourcing,...
The Issue: Lack of assurance of sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.