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. 2,411 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,411 in last 12 months

Showing 3890138920 of 49,744 recalls

FoodFebruary 24, 2015· Lavoi Corporation d/b/a/ Epi De France

Recalled Item: Zaxbys Recalled by Lavoi Corporation d/b/a/ Epi De France Due to Undeclared...

The Issue: Undeclared allergen: Bread products were manufactured using raw material...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 24, 2015· Lavoi Corporation d/b/a/ Epi De France

Recalled Item: Epi breads Recalled by Lavoi Corporation d/b/a/ Epi De France Due to...

The Issue: Undeclared allergen: Bread products were manufactured using raw material...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 24, 2015· Lavoi Corporation d/b/a/ Epi De France

Recalled Item: Epi breads Recalled by Lavoi Corporation d/b/a/ Epi De France Due to...

The Issue: Undeclared allergen: Bread products were manufactured using raw material...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 24, 2015· Lavoi Corporation d/b/a/ Epi De France

Recalled Item: Epi breads Recalled by Lavoi Corporation d/b/a/ Epi De France Due to...

The Issue: Undeclared allergen: Bread products were manufactured using raw material...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 24, 2015· Lavoi Corporation d/b/a/ Epi De France

Recalled Item: Walmart brand bread Recalled by Lavoi Corporation d/b/a/ Epi De France Due...

The Issue: Undeclared allergen: Bread products were manufactured using raw material...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 24, 2015· Maternal Science Inc

Recalled Item: Healthy Mama Boost it Up Pom Cherry Caffeine Free Protein Recalled by...

The Issue: Healthy Mama Brand dietary supplements contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 24, 2015· Maternal Science Inc

Recalled Item: Healthy Mama Boost It Up Mighty Mango Caffeine Free Protein Recalled by...

The Issue: Healthy Mama Brand dietary supplements contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 24, 2015· Maternal Science Inc

Recalled Item: Healthy Mama Boost it Up Mango with Ginger Caffeine Free Recalled by...

The Issue: Healthy Mama Brand dietary supplements contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 23, 2015· Haddon House Food Products Inc

Recalled Item: Twin Tree Gardens Premium Rubs "bunkhouse" Chicken Rub Recalled by Haddon...

The Issue: Haddon House Food Products, Inc. is recalling Twin Tree Gardens Chicken Rub...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 23, 2015· DePuy Orthopaedics, Inc.

Recalled Item: RECLAIM Assembled Implant Inserter Adaptor orthopedic manual surgical...

The Issue: This lot of the RECLAIM Assembled Implant Inserter Adaptor Instrument may...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2015· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Recalled by Medtronic Inc. Cardiac Rhythm Disease Management Due...

The Issue: Clinicians observed debris, appearing to originate from the hemostasis valve...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 23, 2015· Mobius Medical Systems, LP

Recalled Item: Mobius3D Product Usage: Mobius3D software is used for quality assurance...

The Issue: Mobius3D version 1.5.0 contained a defect in software code which affects...

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

Class II — Potential Health HazardOngoing
DrugFebruary 23, 2015· Sagent Pharmaceuticals Inc

Recalled Item: Atracurium Besylate Injection Recalled by Sagent Pharmaceuticals Inc Due to...

The Issue: Lack of Assurance of Sterility: Recall initiated due to FDA observations...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 23, 2015· Qualitest Pharmaceuticals

Recalled Item: PROMETHAZINE DM SYRUP (Promethazine Hydrochloride Recalled by Qualitest...

The Issue: Presence of Foriegn Substance: Plastic cap closure particulates may be...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 23, 2015· Sagent Pharmaceuticals Inc

Recalled Item: Atracurium Besylate Injection Recalled by Sagent Pharmaceuticals Inc Due to...

The Issue: Lack of Assurance of Sterility: Recall initiated due to FDA observations...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 20, 2015· ArthroCare Medical Corporation

Recalled Item: Coblator II System Recalled by ArthroCare Medical Corporation Due to The...

The Issue: The recalling firm was notified by the contract manufacturer that they had...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2015· Abbott Medical Optics, Inc.

Recalled Item: OptiMedica Catalys Precision Laser System Recalled by Abbott Medical Optics,...

The Issue: Device may experience loss of suction during treatment resulting in scoring...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2015· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008 Series Hemodialysis Machines: 2008Kathome - 190895 2008T GEN 2 Recalled...

The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2015· Optimedica Corporation

Recalled Item: Catalys Precision Laser System-Catalys - U - US product Recalled by...

The Issue: Software anomaly on OptiMedica CATALYS System version 3.00.05 that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2015· Fresenius Medical Care Holdings, Inc.

Recalled Item: 2008 Series Hemodialysis Machines: 2008K2 with the following product code...

The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...

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

Class II — Potential Health HazardOngoing