Product Recalls in Maine
Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,529 recalls have been distributed to Maine in the last 12 months.
Showing 6801–6820 of 48,770 recalls
Recalled Item: TactiFlex Ablation Sensor Enabled Ablation Catheter Recalled by St. Jude...
The Issue: When the catheters are used with the EnSiteX EP System, the system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tacrolimus Capsules Recalled by Dr. Reddy's Laboratories, Inc. Due to...
The Issue: Presence of Foreign Tablets/Capsules: One 0.5 mg Tacrolimus capsule found in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ESG PK CUTTING FORCEPS Recalled by Olympus Corporation of the Americas Due...
The Issue: The jaw may fracture prior to the procedure during the inspection instructed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost upgrade- A Multi-functional general Radiography and...
The Issue: Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy...
The Issue: Issue 1: Mixed Images: The Radio Fluoroscopy (RF) viewer may also display a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExcelsiusGPS Cannula A Recalled by Globus Medical, Inc. Due to Devices may...
The Issue: Devices may not be rendered sterile due to an internal gap that may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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: 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.