Product Recalls in Mississippi
Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,661 recalls have been distributed to Mississippi in the last 12 months.
Showing 521–540 of 49,744 recalls
Recalled Item: Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor. Recalled by Philips...
The Issue: It was found that the MX40 device could not reconnect to the PIC iX when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman CereLink ICP Sensor Basic Kit. Catalog Number: 826850. The Recalled...
The Issue: Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558...
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 Calibrators Model/Catalog Number:...
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 pTau217/B-Amyloid 1-42 Plasma Ratio 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 ¿-Amyloid Plasma Controls Model/Catalog Number:...
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 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: 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.