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 3101–3120 of 28,172 recalls
Recalled Item: Healgen Series Reagent strips for Urinalysis are composed of several...
The Issue: The reason for this recall is Healgen Scientific Ltd. has determined that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Code Name: 722282 Azurion 7 M20 722281 Azurion 5 Recalled by PHILIPS...
The Issue: Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Name: 722044 INTEGRIS Allura 15-12 (biplane) 722030 Integris CV...
The Issue: Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Name: 722059 Allura Xper FD20/15 OR Table 722058 Allura Recalled by...
The Issue: Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Name: 708038 MultiDiagnost Eleva with Flat Detector 708037...
The Issue: Potential Detachment of the Cable Hose Carrier (due to broken plastic and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci 5 Recalled by Intuitive Surgical, Inc. Due to Surgical system Error...
The Issue: Surgical system Error 23062 due to connector1) Partially damaged "Potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Gastrointestinal Videoscope Recalled by Olympus Corporation of the...
The Issue: It was discovered during device performance testing that the CCD imaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Horizon Cardiology Hemo. Version 12.2. Recalled by CHANGE HEALTHCARE CANADA...
The Issue: A potential issue has been identified in Change Healthcare Cardiology Hemo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortera Spinal Fixation System Screw Recalled by XTANT Medical Holdings, Inc...
The Issue: Spinal fixation system implant screws marked "DNI" are not intended to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Cardiology Hemo. Versions 14.2 Recalled by CHANGE...
The Issue: A potential issue has been identified in Change Healthcare Cardiology Hemo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson Cardiology Hemo. Versions 13.0 Recalled by CHANGE HEALTHCARE CANADA...
The Issue: A potential issue has been identified in Change Healthcare Cardiology Hemo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur aTPO Assay Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Positive bias in patient results at and below the cut-off of 60 U/mL with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percussionaire Recalled by Percussionaire Corporation Due to Updated...
The Issue: Updated labeling to ensure that blue cap on in-line valve is removed, prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percussionaire Recalled by Percussionaire Corporation Due to Updated...
The Issue: Updated labeling to ensure that blue cap on in-line valve is removed, prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM aTPO Assay Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: Positive bias in patient results at and below the cut-off of 60 U/mL with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BinaxNOW Respiratory Strep A Test Kit Recalled by Cypress Medical Products...
The Issue: Due to a classification error in our inventory management system, these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acceava Respiratory Strep A Recalled by Cypress Medical Products LLC Due to...
The Issue: Due to a classification error in our inventory management system, these...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: basixTOUCH Inflation Device Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Inflation Kit Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: basixSKY Inflation Device Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation devices may have a small hole in the sterile barrier of the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.