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. 2,465 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,465 in last 12 months

Showing 2474124760 of 28,172 recalls

Medical DeviceDecember 5, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Intermittent noise on...

The Issue: Intermittent noise on ECG and/or Respiration waveforms associated with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2013· Symmetry Medical/SSI

Recalled Item: Symmetry and CODMAN brands Recalled by Symmetry Medical/SSI Due to The...

The Issue: The Quad-Lock Sterilization Container System may not maintain an effective...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Intermittent noise on...

The Issue: Intermittent noise on ECG and/or Respiration waveforms associated with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2013· Integra LifeSciences Corp.

Recalled Item: Integra Cusa Excel Rx Only CEM" Nosecone for CUSA¿ Excel Recalled by Integra...

The Issue: The blue COAG button on the CUSA Excel CEM nosecone could stick in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2013· CareFusion 303, Inc.

Recalled Item: Alaris PC unit model 8000 and 8015 with Alaris PCA Recalled by CareFusion...

The Issue: CareFusion is recalling the Alaris PC unit (model 8000 and 8015) because the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 5, 2013· GE Healthcare, LLC

Recalled Item: SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed Recalled by...

The Issue: Intermittent noise on ECG and/or Respiration waveforms associated with...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Cyclosporine Flex reagent cartridge an in vitro diagnostic...

The Issue: Complaints were received regarding variability in recovery of QC and patient...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2013· Philips Medical Systems, Inc.

Recalled Item: Philips Essenta DR Recalled by Philips Medical Systems, Inc. Due to X-ray...

The Issue: X-ray system C-arm casting may loosen and fall

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: PRIMUS Recalled by Siemens Medical Solutions USA, Inc Due to Update to...

The Issue: Update to correct the possibility for patients or operators to have their...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Artis Q and Artis Q biplane systems Product Usage: Recalled by...

The Issue: There exists the possibility that during clinical operation, a breakdown of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Diagnostic imaging systems (GEMINI LXL Model #882412 Recalled by Philips...

The Issue: The PET Reconstruction Server (PRS) database may randomly lock up after the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2013· Sorin Group Deutschland GmbH

Recalled Item: CP5 centrifugal pump system Product Usage: The Stockert S5/ Sorin Recalled...

The Issue: Sorin is initiating a field correction on S5/C5 Heart-lung machine and CP5...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-Ray System (Brilliance CT Big Bore Oncology & Recalled...

The Issue: Machine Name in TumorLOC Basic Mode is obscured. When TumorLOC is in Basic...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2013· Invivo Corporation

Recalled Item: Invivo Corporation Expression Information Portal (Model IP5) is intended to...

The Issue: Invivo Corporation located at 12151 Research Parkway, Orlando, FL 32826 is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2013· Sorin Group Deutschland GmbH

Recalled Item: S5/C5 Heart-lung machine Product Usage: The StOckert S5/ Sorin C5 Recalled...

The Issue: Sorin is initiating a field correction on S5/C5 Heart-lung machine and CP5...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: ADAC ARGUS Gamma Camera Systems & ADAC CIRRUS Gamma Camera Recalled by...

The Issue: The recalling firm determined that visual inspections of the fork joints...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2013· Baxter Corporation Englewood

Recalled Item: ABACUS TPN Calculation Software Recalled by Baxter Corporation Englewood Due...

The Issue: Baxter Healthcare Corporation is issuing a voluntary correction for ABACUS...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach Irrigation Clip 40 Product Usage: Irrigation clips provide a...

The Issue: The Irrigation Clips were assembled with the incorrect (smaller) clips.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2013· Microgenics Corporation

Recalled Item: MAS Omni Immune Controls Recalled by Microgenics Corporation Due to The...

The Issue: The constituent, Inhibin A, was removed from MAS Omni IMMUNE and MAS Omni...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceDecember 2, 2013· Microgenics Corporation

Recalled Item: MAS Omni Immune PRO Controls Recalled by Microgenics Corporation Due to The...

The Issue: The constituent, Inhibin A, was removed from MAS Omni IMMUNE and MAS Omni...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing