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. 1,097 recalls have been distributed to Indiana in the last 12 months.
Showing 15401–15420 of 53,528 recalls
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: BF-N20 OES Bronchofiberscope Recalled by Olympus Corporation of the Americas...
The Issue: The firm is issuing validated, new reprocessing instructions according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AtomLab 500Plus Dose CalibratorSoftware 2.0.00 through Revision 2.0.08...
The Issue: When deleting a previously entered custom isotope, the software deletes the...
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: 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 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: 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: 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: 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: 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: 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: 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: 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: EcoGel 100 - RED Medical Supplies Green Ultrasound Gel Recalled by Red...
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: Ingenia 1.5T- a Magnetic Resonance Medical Electrical Systems indicated for...
The Issue: When using manual mode, the tabletop may not completely move in or out and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.