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. 2,592 recalls have been distributed to Indiana in the last 12 months.
Showing 19921–19940 of 53,528 recalls
Recalled Item: Atellica CH 930 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Editing an assay Test Definition and switching to another assay s Test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4x4 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4oz. Tube Recalled by Gentell, Inc Due to During an FDA...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAVIO Soft Tissue Protector Recalled by Smith & Nephew, Inc. Due to...
The Issue: Potential for the NAVIO Soft Tissue Protector to become stuck or bound to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 2x2 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentell Hydrogel Ag 4x8 Recalled by Gentell, Inc Due to During an FDA audit,...
The Issue: During an FDA audit, it was discovered that the product was not properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Premiere Choice 3lb. Peanut Butter Cookie Dough Recalled by Choice Products...
The Issue: Peanut Butter Cookie Dough may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The CapsoCam Plus (SV-3) Recalled by Capso Vision, Inc. Due to Ingestible...
The Issue: Ingestible video capsule system has capsule with incorrect capture mode...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MYPICC KIT 3F Single-Lumen Recalled by Becton Dickinson & Company Due...
The Issue: The kits contain surgical gowns which were subject to a recall by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MYPICC KIT 5F Dual-Lumen Recalled by Becton Dickinson & Company Due to...
The Issue: The kits contain surgical gowns which were subject to a recall by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MYPICC KIT 5F Dual-Lumen Recalled by Becton Dickinson & Company Due to...
The Issue: The kits contain surgical gowns which were subject to a recall by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MYPICC KIT 5F Triple-Lumen Recalled by Becton Dickinson & Company Due...
The Issue: The kits contain surgical gowns which were subject to a recall by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MYPICC KIT 4F Single-Lumen Recalled by Becton Dickinson & Company Due...
The Issue: The kits contain surgical gowns which were subject to a recall by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MYPICC KIT 5F Triple-Lumen Recalled by Becton Dickinson & Company Due...
The Issue: The kits contain surgical gowns which were subject to a recall by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MYPICC KIT 4F Dual-Lumen Recalled by Becton Dickinson & Company Due to...
The Issue: The kits contain surgical gowns which were subject to a recall by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MYPICC KIT 5F Dual-Lumen Recalled by Becton Dickinson & Company Due to...
The Issue: The kits contain surgical gowns which were subject to a recall by the supplier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartStart MRx Monitor/Defibrillators with model numbers M3535A M3536A...
The Issue: Philips has received a number of reports of HeartStart MRx...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meijer Chicken Cobb Salad 10.75oz. in Clear plastic Recalled by Meijer Due...
The Issue: Undeclared wheat allergen, salad may incorrectly contain a packet of croutons.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nexus Universal with OptiBond Universal Recalled by Kerr/Pentron, DBA Kerr...
The Issue: An issue within production process used to package trial kits let to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoledronic Acid Injection 5 mg/100 mL (0.05 mg/mL) Recalled by Breckenridge...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.