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. 2,524 recalls have been distributed to Maine in the last 12 months.
Showing 7821–7840 of 27,655 recalls
Recalled Item: VERIGENE Enteric Pathogens Nucleic Acid Test Recalled by Luminex Corporation...
The Issue: There is a potential for false negative results using VERIGENE CDF Stool...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethernet cable may be misaligned, the cable jacket (insulation)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: nordicBrainEX Recalled by NordicNeuroLab AS Due to When exporting merged...
The Issue: When exporting merged results from the BOLD, DSC, and DCE modules of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Internal ethernet cable may be misaligned, the cable jacket (insulation)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARS CoV 2 rapid antigen test kits packaged under the Recalled by North...
The Issue: Various brands of SARS CoV 2 Antigen Rapid Test kits were offered for sale...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SurgiCount+ System Application Recalled by Stryker Instruments Div. of...
The Issue: When scanning sponges out after a surgical procedure, an error may allow for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis with software version VD12A. A diagnostic and administrative tool...
The Issue: Sensis/Sensis Vibe SoftwareVD12A, the ComboBox may encounter a disconnect of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe Combo with software version VD12A. A diagnostic and Recalled by...
The Issue: Sensis/Sensis Vibe SoftwareVD12A, the ComboBox may encounter a disconnect of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS Software Version 7.0 SP0.0.4.7 Recalled by GE Healthcare,...
The Issue: The Event Notification Manager (ENM) functionality for certain products does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sight OLO Recalled by SIGHT DIAGNOSTICS LTD Due to The default ranges for...
The Issue: The default ranges for MCH, MCHC, and RDW for age group "Child 2-11y" are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantikine IVD Erythropoietin Human Serum Controls for use as quantitative...
The Issue: The Instructions for Use (IFU, Part Number 750095) provided with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wright EVOLVE TRIAD Plate Cutter Recalled by Wright Medical Technology, Inc....
The Issue: The plate cutter is unable to meet sterilization requirements when it is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haiou Needle Retractable Safety Syringe with Needle-1ML 23G x 1 Recalled by...
The Issue: Complaints received in which needle and needle holder have detached from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HAIOU Needle retractable safety syringe with needle-(1ml syringe with 25G...
The Issue: Complaints received in which needle and needle holder have detached from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Pheno Recalled by Siemens Medical Solutions USA, Inc Due to A video...
The Issue: A video signal from one of the transceivers of the Large Display may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 11B Recalled by RAYSEARCH LABORATORIES AB Due to This notice...
The Issue: This notice concerns two issues found related to the display of Linear...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soluble Transferrin Receptors (STFR) Recalled by Randox Laboratories Ltd....
The Issue: A customer reported a problem with the reagent and calibrator. Randox...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Soluble Transferrin Receptors Calibrator Series (STFR CAL) Recalled by...
The Issue: A customer reported a problem with the reagent and calibrator. Randox...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoolMax ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...
The Issue: Executing a voluntary discontinuation and removal of parallel plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoolFit ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...
The Issue: Executing a voluntary discontinuation and removal of parallel plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.