Product Recalls in Alabama
Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,647 recalls have been distributed to Alabama in the last 12 months.
Showing 7001–7020 of 50,591 recalls
Recalled Item: BrightView Recalled by Philips North America Due to Detector may...
The Issue: Detector may unexpectedly fall due to a component failure. If the detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Recalled by Philips North America Due to Detector may...
The Issue: Detector may unexpectedly fall due to a component failure. If the detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X Recalled by Philips North America Due to Detector may...
The Issue: Detector may unexpectedly fall due to a component failure. If the detector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total immunoglobulin M (IgM total) IVD Recalled by Siemens Healthcare...
The Issue: Potential for a negative bias with quality control (QC) and patient sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PANTHER FUSION System The Panther System is an Recalled by Hologic, Inc. Due...
The Issue: Due to potential false positive Flu B results when a sample was also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Pneumonia Panel Plus (Pneumoplus) Recalled by BioFire Diagnostics,...
The Issue: Their is a potential for false positive results when using Pneumonia panel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Pneumonia Panel (Pneumo) Recalled by BioFire Diagnostics, LLC Due...
The Issue: Their is a potential for false positive results when using Pneumonia panel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Himalayan Pain Relief Tea for Gout and Hangover Recalled by WS Global Inc...
The Issue: Contains undeclared drugs Diclofenac and Dexamethasone Acetate
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Spectral CT 7500: Software Version 5.0 Recalled by PHILIPS MEDICAL SYSTEMS...
The Issue: A software issue that can incorrectly label all captured images that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT on Rails: Software Version 5.1.0.X Recalled by PHILIPS MEDICAL...
The Issue: A software issue that can incorrectly label all captured images that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sedecal X Optima URS digital mobile diagnostic x-ray system. A Recalled by...
The Issue: Some parts have fallen off the equipment resulting in a safety risk to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DiaSorin LIAISON HSV-2 Type Specific IgG Recalled by Diasorin Inc. Due to...
The Issue: DiaSorin has identified that lots 136344, 136344A, 136344B, 136344C, 136520,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Recalled by Maquet Cardiovascular, LLC Due to Express chest drains...
The Issue: Express chest drains are pre-packaged with sterile water syringes which have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Recalled by Maquet Cardiovascular, LLC Due to Express chest drains...
The Issue: Express chest drains are pre-packaged with sterile water syringes which have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANORO ELLIPTA (umeclidinium and vilanterol inhalation powder) 62.5...
The Issue: Failed Release Testing: Coarse Particle Mass for umeclidinium Out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dual Articulating Headrest Recalled by Steris Corporation Due to...
The Issue: Dual-articulating head rest may not stay in place or may fail to lock into...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Articulating Headrest Recalled by Steris Corporation Due to...
The Issue: Dual-articulating head rest may not stay in place or may fail to lock into...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion system Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....
The Issue: System may exhibit a loss of imaging functionality and data due to an issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: High Frequency Transport Phasitron Breathing Circuit Kit Recalled by...
The Issue: Due to an assembly error within the breathing circuit, their pressure output...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE TUBE 4 ml FX Sodium Fluoride/Potassium Oxalate Recalled by Greiner...
The Issue: Tubes have missing additive/anticoagulant resulting in clotting in most...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.