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. 2,641 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,641 in last 12 months

Showing 49614980 of 13,570 recalls

DrugNovember 19, 2019· Baxter Healthcare Corporation

Recalled Item: 0.9% Sodium Chloride Irrigation USP 5000 mL bags Recalled by Baxter...

The Issue: Lack of Assurance of Sterility: Product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 15, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Clobetasol Propionate Foam (Emulsion Formulation) Recalled by Glenmark...

The Issue: Defective delivery system; product is not foaming or is coming out as liquid.

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

Class III — Low RiskOngoing
Refund
DrugNovember 15, 2019· Rising Pharmaceuticals, Inc.

Recalled Item: Timolol Maleate USP Recalled by Rising Pharmaceuticals, Inc. Due to...

The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...

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

Class III — Low RiskOngoing
Refund
DrugNovember 15, 2019· Grato Holdings, Inc.

Recalled Item: Colostat Recalled by Grato Holdings, Inc. Due to Labeling mix-up -...

The Issue: Labeling mix-up - Indications on product label are incorrect.

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

Class III — Low RiskOngoing
Refund
DrugNovember 15, 2019· Rising Pharmaceuticals, Inc.

Recalled Item: Timolol Maleate Sterile Opthalmic Solution Recalled by Rising...

The Issue: Labeling: Label mix-up: A case of Timolol Maleate Sterile Ophthalmic...

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

Class III — Low RiskOngoing
Refund
DrugNovember 15, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Clobetasol Propionate Foam Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: Defective delivery system; product is not foaming or is coming out as liquid.

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

Class III — Low RiskOngoing
Refund
DrugNovember 15, 2019· Akorn, Inc.

Recalled Item: MYORISAN (isotretinoin capsules Recalled by Akorn, Inc. Due to Unit Dose...

The Issue: Unit Dose Mispackaging: Customer complaint that a carton labeled as Myorisan...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 14, 2019· AVKARE Inc.

Recalled Item: AVKARE Ranitidine Tablets Recalled by AVKARE Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 14, 2019· AVKARE Inc.

Recalled Item: AVKARE Ranitidine Tablets Recalled by AVKARE Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 13, 2019· Natures Rx

Recalled Item: Silver Bullet Recalled by Natures Rx Due to Undeclared Active

The Issue: Marketed Without an Approved NDA/ANDA; Product contains undeclared active...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 13, 2019· Precision Dose Inc.

Recalled Item: Ranitidine Oral Solution Recalled by Precision Dose Inc. Due to CGMP...

The Issue: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2019· QuVa Pharma, Inc.

Recalled Item: fentaNYL 250 mcg/5 mL (50 mcg/mL) Recalled by QuVa Pharma, Inc. Due to...

The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API due to...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2019· Integrated Health Concepts Inc. dba Conversio Health

Recalled Item: Albuterol 2.5mg / Budesonide 0.5mg Recalled by Integrated Health Concepts...

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2019· Integrated Health Concepts Inc. dba Conversio Health

Recalled Item: Albuterol 2.5mg / Ipratropium 0.75mg Recalled by Integrated Health Concepts...

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2019· Integrated Health Concepts Inc. dba Conversio Health

Recalled Item: Albuterol 2.5mg / Ipratropium 0.75mg/ Triamcinolone 0.5 mg 3ML Vial Recalled...

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2019· Integrated Health Concepts Inc. dba Conversio Health

Recalled Item: Albuterol 1.25mg / Ipratropium 0.5mg/ Budesonide 0.25mg Recalled by...

The Issue: Lack of Processing Controls

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2019· QuVa Pharma, Inc.

Recalled Item: fentaNYL 2500 mcg/250 mL (10 mcg/mL) in 0.9% Sodium Chloride Recalled by...

The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API due to...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2019· QuVa Pharma, Inc.

Recalled Item: fentaNYL 500 mcg/250 mL (2 mcg/mL) ROPivacaine HCl 0.2% 500 Recalled by QuVa...

The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API due to...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2019· QuVa Pharma, Inc.

Recalled Item: fentaNYL 2000 mcg/100 mL (20 mcg/mL) in 0.9% Sodium Chloride Recalled by...

The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API due to...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 12, 2019· QuVa Pharma, Inc.

Recalled Item: fentaNYL 2750 mcg/55 mL (50 mcg/mL) 55 mL Syringe Recalled by QuVa Pharma,...

The Issue: Presence of Particulate matter: manufacturer recalled fentanyl API due to...

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

Class II — Potential Health HazardOngoing
Refund