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. 2,661 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,661 in last 12 months

Showing 16011620 of 49,744 recalls

DrugAugust 20, 2025· Baxter Healthcare Corporation

Recalled Item: Acetaminophen Injection 1000 mg/100 mL (10 mg/mL) Recalled by Baxter...

The Issue: Discoloration

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 20, 2025· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: Carvedilol Tablets USP Recalled by The Harvard Drug Group LLC dba Major...

The Issue: CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 20, 2025· MicroSurgical Technology Inc

Recalled Item: MST ArcDUO 9mm Recalled by MicroSurgical Technology Inc Due to An ophthalmic...

The Issue: An ophthalmic knife has a suction set (not direct patient-contacting), which...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2025· Abiomed, Inc.

Recalled Item: Automated Impella Controller (AIC) with the below brands and product...

The Issue: Specific Automated Impella Controllers (AICs) that have a Pump Driver...

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

Class I — Serious Health HazardOngoing
DrugAugust 19, 2025· Medline Industries, LP

Recalled Item: READYPREP PVP Recalled by Medline Industries, LP Due to Subpotent drug

The Issue: Subpotent drug

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 19, 2025· Greiner Bio-One North America, Inc.

Recalled Item: Brand Name: Vacuette Product Name: 8 ml CAT Serum Separator Recalled by...

The Issue: Some of the Vacuette¿ CAT Serum Separator Clot Activator tubes were...

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

Class II — Potential Health HazardOngoing
DrugAugust 18, 2025· B BRAUN MEDICAL INC

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B BRAUN MEDICAL INC Due to...

The Issue: Presence of Particulate Matter.

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 18, 2025· Amneal Pharmaceuticals, LLC

Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...

The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 18, 2025· Amneal Pharmaceuticals, LLC

Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...

The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 18, 2025· Amneal Pharmaceuticals, LLC

Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...

The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 18, 2025· Amneal Pharmaceuticals, LLC

Recalled Item: Sulfamethoxazole and Trimethoprim Tablets Recalled by Amneal...

The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 18, 2025· Amneal Pharmaceuticals, LLC

Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Amneal Pharmaceuticals, LLC...

The Issue: Presence of a foreign substance.A specific lot of auxiliary polyester coil,...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 18, 2025· B BRAUN MEDICAL INC

Recalled Item: Lactated Ringers's Injection USP Recalled by B BRAUN MEDICAL INC Due to...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 18, 2025· CORNEAT VISION, LTD.

Recalled Item: CorNeat EverPatch Recalled by CORNEAT VISION, LTD. Due to Reviewed...

The Issue: Reviewed complaints have identified that conjunctival wound dehiscence may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2025· CORNEAT VISION, LTD.

Recalled Item: EverPatch+ Recalled by CORNEAT VISION, LTD. Due to Reviewed complaints have...

The Issue: Reviewed complaints have identified that conjunctival wound dehiscence may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2025· Boston Scientific Corporation

Recalled Item: ICEfx Cryoablation System Recalled by Boston Scientific Corporation Due to...

The Issue: Certain desiccant tube subassemblies were built with end caps that were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2025· Boston Scientific Corporation

Recalled Item: Preventive Maintenance (PM) Kit ICEFX Recalled by Boston Scientific...

The Issue: Certain desiccant tube subassemblies were built with end caps that were not...

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

Class II — Potential Health HazardOngoing
FoodAugust 15, 2025· Anderson Candy Company, LLC

Recalled Item: Peanut rounds 2.25 oz and 3 oz Recalled by Anderson Candy Company, LLC Due...

The Issue: Undeclared soy allergen

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 15, 2025· Maquet Cardiovascular, LLC

Recalled Item: Heartstring III Proximal Seal System. Intravascular anastomosis occluder....

The Issue: Three failure modes have been identified: failure of the Heartstring Seal to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 15, 2025· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: BeneVision N1 Patient Monitor (N1). Part Numbers: 6660E-PA00017 Recalled by...

The Issue: Potential for activation of an abnormal alarm pause.

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

Class II — Potential Health HazardOngoing