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. 2,358 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,358 in last 12 months

Showing 4822148240 of 49,744 recalls

Medical DeviceAugust 9, 2012· Omni Life Science

Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...

The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Omni Life Science

Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...

The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Omni Life Science

Recalled Item: Omnilife Science Apex Knee System Modular Tibia Augment Recalled by Omni...

The Issue: The Apex Knee System Modular Tibia Augment may breach the inner and outer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· Intuitive Surgical, Inc.

Recalled Item: Tip Cover for 8mm Monopolar Curved Scissors (Hot Shears)Accessory Recalled...

The Issue: There is potential for the sterility of the product to be compromised.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· AmeriWater Inc

Recalled Item: AmeriWater MRO Dialysis RO+ System Recalled by AmeriWater Inc Due to The...

The Issue: The firm was notified that a malfunction of the device was caused by an...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2012· AGFA Corp.

Recalled Item: AGFA IMPAC CV DICOMStore with Media Purge Daemon (MPD) and Recalled by AGFA...

The Issue: Loss of patient data can occur under certain circumstances due to...

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

Class II — Potential Health HazardOngoing
FoodAugust 8, 2012· American Importing Co, Inc

Recalled Item: Nature's Harvest Recalled by American Importing Co, Inc Due to Undeclared...

The Issue: Amport Foods is recalling one lot of pine nuts because there may be...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 8, 2012· Parks Medical Electronics, Inc

Recalled Item: Devices includes a Multi Port Inflator or without Multi Port Recalled by...

The Issue: Parks Medical Electronics, Inc. was made aware of two incidents where an air...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Positron Emission Tomography (PET) and X-ray Computed Tomography Recalled by...

The Issue: Philips became aware of an issue relating to a UPS battery cabinet that...

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

Class II — Potential Health HazardOngoing
DrugAugust 7, 2012· Mylan Pharmaceuticals Inc.

Recalled Item: Doxazosin Tablets Recalled by Mylan Pharmaceuticals Inc. Due to Cross...

The Issue: Cross Contamination w/Other Products: During stability testing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 7, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare conducted...

The Issue: GE Healthcare conducted a recall on various mobile x-ray units (Optima...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Prolactin Assay: ADVIA Centaur Calibrator B Catalog Number....

The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...

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

Class III — Low RiskOngoing
Medical DeviceAugust 7, 2012· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur FSH Assay: ADVIA Centaur Calibrator B US: Calibrator Recalled...

The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...

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

Class III — Low RiskOngoing
Medical DeviceAugust 6, 2012· Orthofix, Inc

Recalled Item: Orthofix ISKD Limb Lengthener. ISKD - Intramedullary Skeletal Kinetic...

The Issue: There is a possibility that the ISKD limb lengthener may stop distracting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Synthes USA HQ, Inc.

Recalled Item: Synthes(R) Spine Vectra Recalled by Synthes USA HQ, Inc. Due to Although the...

The Issue: Although the reported incidence is low, there is the potential for the drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Synthes USA HQ, Inc.

Recalled Item: Synthes(R) Spine Vectra Recalled by Synthes USA HQ, Inc. Due to Although the...

The Issue: Although the reported incidence is low, there is the potential for the drill...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Howmedica Osteonics Recalled by Stryker Howmedica Osteonics Corp....

The Issue: During the manufacturing of the affected lot a manufacturing error has led...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· ThyssenKrupp Access Corp

Recalled Item: ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically...

The Issue: The seat could break as a result of damage resulting from a seat belt being...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Diamedix Corporation

Recalled Item: The Is-anti-Sm test kits****Catalog No: 720-240*** Product Usage: The...

The Issue: Diamedix Corporation recalled their Is-anti-Sm Test Kit due to the Positive...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2012· Invacare Corporation

Recalled Item: Invacare¿ I-Fit" Shower Chair (Models 9780 Recalled by Invacare Corporation...

The Issue: On August 6, 2012, Invacare voluntarily recalled the Invacare¿ I-Fit" Shower...

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

Class II — Potential Health HazardOngoing