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. 1,011 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
1,011 in last 12 months

Showing 28081–28100 of 49,744 recalls

Medical DeviceJune 30, 2017· Elekta, Inc.

Recalled Item: MOSAIQ Medical Charged-Particle Radiation Therapy System Recalled by Elekta,...

The Issue: The table shift in the vertical direction was inverted during the use of CMA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Alcon Research, Ltd.

Recalled Item: ORA System with VerifEye+ Cart Recalled by Alcon Research, Ltd. Due to Some...

The Issue: Some ORA Carts have the potential to return an incorrect IOL power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Alcon Research, Ltd.

Recalled Item: ORA System with VerifEye Recalled by Alcon Research, Ltd. Due to Some ORA...

The Issue: Some ORA Carts have the potential to return an incorrect IOL power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Sorin Group USA, Inc.

Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...

The Issue: Plastic heat exchanger fibers separating the blood compartment from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Sorin Group USA, Inc.

Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...

The Issue: Plastic heat exchanger fibers separating the blood compartment from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Sorin Group USA, Inc.

Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...

The Issue: Plastic heat exchanger fibers separating the blood compartment from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Sorin Group USA, Inc.

Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...

The Issue: Plastic heat exchanger fibers separating the blood compartment from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Sorin Group USA, Inc.

Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...

The Issue: Plastic heat exchanger fibers separating the blood compartment from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2017· Sorin Group USA, Inc.

Recalled Item: STOCKERT Heater-Cooler System 3T Recalled by Sorin Group USA, Inc. Due to...

The Issue: Plastic heat exchanger fibers separating the blood compartment from the...

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

Class II — Potential Health HazardOngoing
DrugJune 29, 2017· Teva Pharmaceuticals USA

Recalled Item: Buprenorphine and Naloxone Sublingual Tablets Recalled by Teva...

The Issue: Failed Impurities/Degradation Specifications: out of specification test...

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

Class III — Low RiskOngoing
Refund
DrugJune 29, 2017· Teva Pharmaceuticals USA

Recalled Item: Buprenorphine and Naloxone Sublingual Tablets 8 mg/2 mg 30 tablets per...

The Issue: Failed Impurities/Degradation Specifications: out of specification test...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 29, 2017· Roche Diagnostics Corporation

Recalled Item: Brand Name: ¿ cobas c 6000 MODULAR Series System e Recalled by Roche...

The Issue: Roche has confirmed that a possible sample mismatch issue may occur on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic ENT Prgm 9734636 Add Fusion Nav AxiEM Recalled by Medtronic...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic Instrument Set EM ENT Recalled by Medtronic Navigation, Inc. Due...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic Suction 9734308 Small AxiEM ENT Recalled by Medtronic Navigation,...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic Curved Suction 90 9733451 EM ENT Recalled by Medtronic Navigation,...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic Set Supplemental INS AxiEM ENT Recalled by Medtronic Navigation,...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic Instrument Kit 9733908 Fusion ENT Recalled by Medtronic...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic Curved Suction 70 9733450 EM ENT Recalled by Medtronic Navigation,...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2017· Medtronic Navigation, Inc.

Recalled Item: Medtronic Straight Suction 9733449 EM ENT Recalled by Medtronic Navigation,...

The Issue: The instruments are not able to pass instrument verification which is...

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

Class II — Potential Health HazardOngoing