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. 2,460 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,460 in last 12 months

Showing 2612126140 of 49,744 recalls

FoodMarch 29, 2018· purely elizabeth.

Recalled Item: Chocolate Sea Salt Probiotic Granola Recalled by purely elizabeth. Due to...

The Issue: Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 29, 2018· Akorn, Inc.

Recalled Item: 24-HOUR Oral Care q4 Kit with Ballard* Technology Recalled by Akorn, Inc....

The Issue: Subpotent Drug: Product crystallization with accompanying low out of...

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

Class III — Low RiskOngoing
Refund
DrugMarch 29, 2018· Akorn, Inc.

Recalled Item: Chlorhexidine Gluconate Oral Rinse Recalled by Akorn, Inc. Due to Subpotent...

The Issue: Subpotent Drug: Product crystallization with accompanying low out of...

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

Class III — Low RiskOngoing
Refund
DrugMarch 29, 2018· United Pacific Co Ltd

Recalled Item: Zhong Hua Jiu (menthol 1%) Patch Recalled by United Pacific Co Ltd Due to...

The Issue: CGMP Deviations: the product was produced with substandard GMP manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 29, 2018· Akorn, Inc.

Recalled Item: 24-HOUR Oral Care q2 Kit with Ballard* Technology Recalled by Akorn, Inc....

The Issue: Subpotent Drug: Product crystallization with accompanying low out of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 29, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Segmental System Proximal Femoral Component 38mm Offset Recalled by...

The Issue: There is a potential for debris in the hole on the superior lateral aspect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2018· Stryker Sustainability Solutions

Recalled Item: Coronary Sinus (CS) Uni-Directional Diagnostic Electrophysiology (EP)...

The Issue: Thrombogenicity test results demonstrated that both the test devices (SSS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Draegar Medical Systems, Inc.

Recalled Item: Infinity Acute Care System (lACS) Monitoring Solution Recalled by Draegar...

The Issue: Software anomaly resulting in the loss of patient settings and stored...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...

The Issue: The dose calculation accuracy may in some situations be less than expected....

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

Class II — Potential Health HazardOngoing
DrugMarch 28, 2018· Elroselabs Inc.

Recalled Item: Conzerol zero molluscum contagiosum Recalled by Elroselabs Inc. Due to cGMP...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 28, 2018· Elroselabs Inc.

Recalled Item: Molleave Recalled by Elroselabs Inc. Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 28, 2018· Elroselabs Inc.

Recalled Item: Conzerol (antipoxin) H2O2 Gel Recalled by Elroselabs Inc. Due to cGMP Deviations

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 27, 2018· AuroMedics Pharma LLC

Recalled Item: Levetiracetam in 0.75% Sodium Chloride Injection Recalled by AuroMedics...

The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 27, 2018· AuroMedics Pharma LLC

Recalled Item: Levetiracetam in 0.82% Sodium Chloride Injection Recalled by AuroMedics...

The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...

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

Class II — Potential Health HazardOngoing
Refund