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. 2,562 recalls have been distributed to Maine in the last 12 months.
Showing 521–540 of 48,770 recalls
Recalled Item: Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Immunoreaction Cartridges...
The Issue: Customers may experience inaccurate test results by observing a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators Model/Catalog...
The Issue: Customers may experience inaccurate test results by observing a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Lumipulse G pTau 217 Plasma Immunoreaction Cartridges...
The Issue: Customers may experience inaccurate test results by observing a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kii Low Profile Recalled by Applied Medical Resources Corp Due to There is...
The Issue: There is the potential for extended length of the blade obturator after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The product is used for the evaluation of the intrinsic coagulation pathway...
The Issue: Potential for microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mazor X robotic guidance system Recalled by Mazor Robotics Ltd Due to...
The Issue: Software errors that can result in incorrect surgical instrument positioning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System with Particle Therapy License (License...
The Issue: Using oncology information system that manages workflow may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ciclopirox Shampoo Recalled by SUN PHARMA /TARO Due to Failed...
The Issue: Failed Impurity/Degradation specifications: OOS results obtained at the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The LDL-Cholesterol assay is comprised of two distinct phases. In Recalled...
The Issue: Beckman Coulter identified that LDL Cholesterol OSR6x96 is not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Systems R3.0. Includes the following label descriptions and...
The Issue: Nine (9) identified software issues which may result in the following: loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HFD100 Product Name: Head Fixation Device HFD100 Model/Catalog...
The Issue: Torque screw may crack or separate. If used, an affected screw could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial 900 MHz Call Station Recalled by Securitas Healthcare LLC Due to...
The Issue: Securitas Healthcare has become aware of a firmware issue in the Call...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial 900 MHz Call Station Recalled by Securitas Healthcare LLC Due to...
The Issue: Securitas Healthcare has become aware of a firmware issue in the Call...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog...
The Issue: Incorrect expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revogene C. difficile Recalled by Meridian Bioscience Inc Due to The...
The Issue: The affected lots show a decline in performance over time, which may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Leos Laser and Endoscopy System. Model Number: OME6000U. Recalled by...
The Issue: Manufacturing deviation in which the ferrites specified for the USB cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jumbo RAW SHRIMP Recalled by AZ Gems, Inc. Due to elevated levels of...
The Issue: elevated levels of chloramphenicol in frozen shrimp
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Inflation...
The Issue: Inflation device handle may detach from the syringe during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allwell Inflation Device Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation device handle may detach from the syringe during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Numbers:...
The Issue: Inflation device handle may detach from the syringe during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.