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. 2,658 recalls have been distributed to Indiana in the last 12 months.
Showing 15401–15420 of 53,528 recalls
Recalled Item: syngo.CT VA20A Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Potential for data loss when using the contouring or patient marking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.via RT Image Suite with syngo.via VB30 Recalled by Siemens Medical...
The Issue: Potential for data loss when using the contouring or patient marking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR MAGNETOM Systems with RT Image Suite with syngo MR VA20A Recalled by...
The Issue: Potential for data loss when using the contouring or patient marking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chantix (varenicline) tablets 0.5mg Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chantix (varenicline) tablets 1 mg Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chantix (varenicline) tablets 0.5mg/1mg Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chantix (varenicline) tablets 1 mg Recalled by Pfizer Inc. Due to CGMP...
The Issue: CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Betamethasone Dipropionate Lotion USP (Augmented) Recalled by Akorn, Inc....
The Issue: Failed impurities/degradation specification: Out of Specification for an...
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 Specifications: Out of Specification impurity results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvedilol Tablets Recalled by Zydus Pharmaceuticals (USA) Inc Due to...
The Issue: Presence of Foreign Tablets/Capsules; report of two Paroxetine tablets were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hostess Soft White Hot Dog Buns Recalled by Hostess Brands, LLC Due to...
The Issue: The firm's contract manufacturer found positive environmental samples...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hostess Soft White Hamburger Buns Recalled by Hostess Brands, LLC Due to...
The Issue: The firm's contract manufacturer found positive environmental samples...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Imperative Care Recalled by IMPERATIVE CARE INC Due to There is a potential...
The Issue: There is a potential for distal end of catheters to fracture and become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Allura Xper series is intended for use on human Recalled by Philips...
The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Azurion series (within the limits of the used Operation Recalled by...
The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lyra Direct SARS-CoV-2 Assay Emergency Use Authorization- . The Recalled by...
The Issue: Revised Instructions for Use: Potential for specimens from patients with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Allura Xper series is intended for use on human Recalled by Philips...
The Issue: Early life failure of the ADUs only occurs when the hospital mains provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EcoGel 100 Imaging Gel Recalled by AMTEC SALES Inc Due to Ultrasound gels...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydro Pinapple Burn Max Health Thach Dua Recalled by Ebay Seller - John...
The Issue: Marketed without an approved NDA/ ANDA - presence of undeclared sibutramine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gordon Choice Deli Style Tuna Salad Recalled by RMH Foods Due to Undeclared...
The Issue: Undeclared wheat and tuna
Recommended Action: Do not consume. Return to store for a refund or discard.