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. 2,476 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,476 in last 12 months

Showing 2350123520 of 28,172 recalls

Medical DeviceAugust 13, 2014· Volcano Corporation

Recalled Item: Volcano TrakBack II Disposable Pullback Device Recalled by Volcano...

The Issue: Internal testing had identified a potential breach to the sterile barrier...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Siemens Healthcare Diagnostics

Recalled Item: ADVIA Centaur XP Immunoassay System Recalled by Siemens Healthcare...

The Issue: The firm is conducting a field correction for the ADVIA Centaur and ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: V5Ms Transesophageal transducers Recalled by Siemens Medical Solutions USA,...

The Issue: Reports of deterioration of material covering the articulating section of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Maquet Cardiovascular, LLC

Recalled Item: Acrobat V Vacuum Off-Pump System OM-9100S Acrobat SUV Vacuum Off-Pump...

The Issue: An internal finding identified the presence of pinholes/cuts in some of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Vapotherm, Inc.

Recalled Item: Vapotherm Precision Flow Recalled by Vapotherm, Inc. Due to Disposable...

The Issue: Disposable Patient Circuit that allows water to leak into the center gas lumen

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 13, 2014· Smith & Nephew, Inc.

Recalled Item: RENASYS EZ Negative Pressure Wound Therapy (NPWT) System (RENASYS EZ)...

The Issue: Modification were made to the RENASYS EZ NPWT Systems without a 510(k) or...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Luminos dRF system with SW VD10 or on Luminos Recalled by Siemens...

The Issue: It was determined that a potential malfunction may occur on the Luminos dRF...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2014· Ethicon Endo-Surgery Inc

Recalled Item: PROXIMATE Skin Stapler. PROXIMATE RH Rotating-Head Skin Stapler (Model...

The Issue: The device may have a non-conforming component that may cause the device to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2014· Gendex Corp

Recalled Item: eXpertDC intraoral x-ray Recalled by Gendex Corp Due to Two (2) failures of...

The Issue: Two (2) failures of the spring link components within the articulated arm...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2014· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX PENTRA Magnesium RTU Reagent Recalled by Horiba Instruments, Inc dba...

The Issue: Horiba Medical is recalling the ABX PENTRA Magnesium RTU Reagent because the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2014· ELITech Clinical Systems SAS

Recalled Item: ENVOY 500 AST Reagent Kit Recalled by ELITech Clinical Systems SAS Due to...

The Issue: Some users of ENVOY 500 AST Reagent Kit, 55255, for Envoy 500 systems are...

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

Class III — Low RiskOngoing
Medical DeviceAugust 11, 2014· Instradent USA, Inc.

Recalled Item: Neodent Titamax WS Cortical Implant ¿4.0 x 5 mm (Endosseous Recalled by...

The Issue: Product not approved for use in the US

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· CareFusion 203, Inc.

Recalled Item: CareFusion EnVe and ReVel Ventilators. The EnVe/ ReVel Ventilator is...

The Issue: CareFusion has identified a potential for damage to the power connector on...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 8, 2014· Beckman Coulter, Inc.

Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...

The Issue: Technical Support Bulletin issued in February 2013 did not mention...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· Beckman Coulter, Inc.

Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...

The Issue: Technical Support Bulletin issued in February 2013 did not mention...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· Beckman Coulter, Inc.

Recalled Item: MicroScan Microbiology Systems: Dried Gram Negative MIC/Combo Panels...

The Issue: Technical Support Bulletin issued in February 2013 did not mention...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2014· Bard Access Systems

Recalled Item: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the Recalled by Bard...

The Issue: Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit...

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

Class II — Potential Health HazardOngoing