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. 2,623 recalls have been distributed to Mississippi in the last 12 months.
Showing 8841–8860 of 28,172 recalls
Recalled Item: Aspiration Syringe Kit Recalled by MICROVENTION INC. Due to Syringe Kits...
The Issue: Syringe Kits labeled for distribution OUS were inadvertently shipped to US...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nimbus PainPro Ambulatory Infusion Pumps with software version v4 Recalled...
The Issue: An unreleased Version 4 Protocol Library was installed on Nimbus PainPro (H)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model B35200 - Percept PC BrainSense Implantable Neurostimulator Recalled by...
The Issue: During cardioversion events, the Model B35200 Percept PC Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas u 601 urinalysis test system Recalled by Roche Diagnostics Operations,...
The Issue: A potential risk for false negative nitrite results exists when endogenous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Karl Storz Udel Sterilization Tray Instructions for Use Recalled by Karl...
The Issue: To ensure sterilization effectiveness, sterilization tray instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 500- In-vitro diagnostic device intended to duplicate manual...
The Issue: Incorrect Default Hemolysis, Icterus or Lipemia (HIL) Index for Five...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista 1500 In-vitro diagnostic device intended to duplicate manual...
The Issue: Incorrect Default Hemolysis, Icterus or Lipemia (HIL) Index for Five...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Centricity Universal Viewer Zero Footprint Client Recalled by GE...
The Issue: There is a potential to display incomplete patient imaging study.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant II Stent Graft System REF/Description: ETBF2513C145EE STENT GRAFT...
The Issue: Due to, during stent graft deployment, the spindle may detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT...
The Issue: During stent graft deployment, the spindle may detach from the distal end of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endurant IIs Stent Graft System REF/Description: ESBF2814C103EE STENT GRAFT...
The Issue: Due to, during stent graft deployment, the spindle may detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MobileDiagnost wDR Recalled by SEDECAL SA Due to While cleaning or...
The Issue: While cleaning or disinfecting the system, if the process is not followed as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: These are communication systems Recalled by Hill-Rom Inc. Due to An...
The Issue: An unrecoverable error may occur where a component will fail to complete the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IPL Coupling Gel Recalled by Lumenis, Inc. Due to Ultrasound gels and...
The Issue: Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arietta 850 Ultrasound- Software Version: V1.0.0 through V4.1.3 Recalled by...
The Issue: Diagnostic ultrasound system with the specified software version and used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lisendo 880 Ultrasound Software Version: V1.0 through V4.1.3 Recalled by...
The Issue: Diagnostic ultrasound system with the specified software version and used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arietta 750 Ultrasound Software Version: V1.0.0 through V2.1.3 Recalled by...
The Issue: Diagnostic ultrasound system with the specified software version and used in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arietta 65 Ultrasound Software Versions: V1.0 through V4.0.0 Recalled by...
The Issue: When the ultrasound system is used in combination with a Fujifilm (formally...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Skinny Needle with Chiba Tip. RPN 090010 Recalled by Cook Inc. Due to...
The Issue: Specific lots may contain black debris on the exterior of the inner stylet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL ReadiPlasTin (20 mL) Recalled by Instrumentation Laboratory Due to...
The Issue: The firm has received customer reports of performance issues with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.