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. 2,695 recalls have been distributed to Indiana in the last 12 months.
Showing 13881–13900 of 53,528 recalls
Recalled Item: Exaprin pain reliever (acetaminophen 110 mg Recalled by Ultra Seal...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SINU-PHEN PLUS sinus pain and congestion tabs (acetaminophen 500 mg Recalled...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cold Relief Severe Pain/Cough (acetaminophen 325mg Recalled by Ultra Seal...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AYPANAL Non-aspirin Pain Reliever (acetaminophen 325 mg) tablets Recalled by...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Regular Strength Pain Reliever (acetaminophen 110 mg Recalled by Ultra Seal...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cold Tablet Pain Reliever/Fever Reducer/Expectorant/Nasal Decongestant...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SINUS DECONGESTANT Nasal Decongestant (phenylephrine HCl 5mg) tablets...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: REMfresh Advanced Ion-Powered Melatonin (Melatonin 5 mg) Caplets Recalled by...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CETAFEN COUGH & COLD COUGH & COLD RELIEF (Acetaminophen 325 mg Recalled by...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ELECTROLYTE Supplement Tablets (calcium 5.2 mg Recalled by Ultra Seal...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Multi-Symptom Cramp Relief (acetaminophen 325mg and Pamabrom 25mg) Recalled...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips Respironics V60 Plus Ventilator Part Number 1138747 Recalled by...
The Issue: A limited number of ventilators were assembled with expired adhesive. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number 1053617 Recalled by...
The Issue: A limited number of ventilators were assembled with expired adhesive. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6" Recalled by...
The Issue: Guidewire included with two lots of Arterial Line Kits would not fit through...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proctofoam HC (hydrocortisone acetate 1% and pramoxine hydrochloride 1%)...
The Issue: cGMP deficiencies
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Codman Cranial Access Kits- indicated when a craniotomy is required Recalled...
The Issue: Incorrect extended expiration dates identified on the outer box label only,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Cranial Access Kits- indicated when a craniotomy is required Recalled...
The Issue: Incorrect extended expiration dates identified on the outer box label only,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuMoDx Flu A-B/RSV/SARS-CoV-2 Vantage Test Strip Recalled by NeuMoDx...
The Issue: A risk for product contamination was identified for the affected product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Sight OLO device is a computer vision based platform Recalled by SIGHT...
The Issue: In instances where custom ranges were configured on the device post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BenchMark ULTRA and DISCOVERY ULTRA Instruments Recalled by Ventana Medical...
The Issue: Potential for Fluid Leak inside a staining system that could cause an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.