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. 2,635 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,635 in last 12 months

Showing 54015420 of 13,570 recalls

DrugAugust 9, 2019· Ridge Properties, LLC

Recalled Item: Superior Pain & Itch Relief (lidocaine) Cream Recalled by Ridge Properties,...

The Issue: Superpotent Drug: products were found to be contaminated and above...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2019· Ridge Properties, LLC

Recalled Item: Soothing Sore Relief (lidocaine) Cream Recalled by Ridge Properties, LLC Due...

The Issue: Superpotent Drug: products were found to be contaminated and above...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2019· Ridge Properties, LLC

Recalled Item: PRE-TAT (lidocaine) 3 in 1 Pre Tattoo Prep With Lidocaine Liquid Gel...

The Issue: Microbial Contamination of Non-Sterile Products: products were found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2019· American Health Packaging

Recalled Item: Carbamazepine Recalled by American Health Packaging Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2019· Ridge Properties, LLC

Recalled Item: PRE-TAT (lidocaine) 3 in 1 Pre Tattoo Prep With Lidocaine Cream Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products: products were found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 9, 2019· Ridge Properties, LLC

Recalled Item: Superior Pain & Itch Relief (lidocaine) Liquid Gel Recalled by Ridge...

The Issue: Superpotent Drug: products were found to be contaminated and above...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 8, 2019· Alkermes Inc

Recalled Item: Vivitrol (naltrexone for extended-release injectable suspension) 380...

The Issue: Labeling: Not Elsewhere Classified. Drug product kit recalled due to 1 inch...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Clotrimazole and Betamethasone Dipropionate Cream USP Recalled by Glenmark...

The Issue: Temperature Abuse: Complaints received of liquidy texture.

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2019· Akorn, Inc.

Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Short Fill: fill...

The Issue: Short Fill: fill volume was out of specification at 94 mL (specification: no...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2019· Akorn, Inc.

Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for...

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

Class III — Low RiskOngoing
Refund
DrugAugust 6, 2019· Akorn, Inc.

Recalled Item: Eptifibatide Injection Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification (OOS) for...

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

Class III — Low RiskOngoing
Refund
DrugJuly 29, 2019· Aurobindo Pharma USA Inc.

Recalled Item: Simvastatin Tablets Recalled by Aurobindo Pharma USA Inc. Due to Labeling;...

The Issue: Labeling; Incorrect or Missing Lot and/or Exp Date; some bottles labeled...

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

Class III — Low RiskOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Assorted IRC Display Recalled by Medtech Products, Inc. Due to...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Assorted Sidekick Floor Stand Display Recalled by Medtech...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Maximum Itchy Eye Relief Sidekick Floor Stand Display Recalled by...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Redness Relief Handy Pocket Pal Club Pak Display Recalled by...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes REDNESS RELIEF (Glycerin 0.25% Recalled by Medtech Products, Inc....

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Maximum Redness and Itchy Eye Relief Sidekick Display Recalled by...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear eyes MAXIMUM ITCHY EYE RELIEF (Glycerin 0.25% Recalled by Medtech...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2019· Medtech Products, Inc.

Recalled Item: Clear Eyes Redness Relief Hand Pocket Pal Tray Display Recalled by Medtech...

The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...

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

Class II — Potential Health HazardOngoing
Refund