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. 2,591 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,591 in last 12 months

Showing 1260112620 of 49,744 recalls

Medical DeviceApril 11, 2022· Umano Medical, Inc.

Recalled Item: AC-powered adjustable medical beds with built-in electric DC actuators and...

The Issue: There is a potential hazard of uninterrupted motion of the Motorized Wheel...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2022· TELEFLEX MEDICAL INC

Recalled Item: (1) Gibeck Humid-Vent 2S Flex DC Recalled by TELEFLEX MEDICAL INC Due to...

The Issue: Reports received of torn corrugated breathing tubes.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2022· TELEFLEX MEDICAL INC

Recalled Item: (1) Teleflex Flex tube Recalled by TELEFLEX MEDICAL INC Due to Reports...

The Issue: Reports received of torn corrugated breathing tubes.

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

Class II — Potential Health HazardOngoing
FoodApril 8, 2022· Eastland Food Corporation

Recalled Item: Bwell Bird's Nest Beverage Sugar-Free Xylitol NET 8.45 FL OZ Recalled by...

The Issue: Deficient packaging material potentially leading to premature spoilage.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 8, 2022· Eastland Food Corporation

Recalled Item: Bwell Bird's Nest Beverage Pandan Flavor NET 8.45 FL OZ Recalled by Eastland...

The Issue: Deficient packaging material potentially leading to premature spoilage.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 8, 2022· Eastland Food Corporation

Recalled Item: Bwell Bird's Nest Beverage Honey Flavor NET 8.45 FL OZ Recalled by Eastland...

The Issue: Deficient packaging material potentially leading to premature spoilage.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 8, 2022· Eastland Food Corporation

Recalled Item: Bwell Bird's Nest Beverage Lychee Flavor NET 8.45 FL OZ Recalled by Eastland...

The Issue: Deficient packaging material potentially leading to premature spoilage.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 8, 2022· Eastland Food Corporation

Recalled Item: Bwell Bird's Nest Beverage Rock Sugar Flavor NET 4.45 FL Recalled by...

The Issue: Deficient packaging material potentially leading to premature spoilage.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 8, 2022· Eastland Food Corporation

Recalled Item: Bwell Bird's Nest Beverage Coconut Flavor NET 8.45 FL OZ Recalled by...

The Issue: Deficient packaging material potentially leading to premature spoilage.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 8, 2022· Radiometer Medical ApS

Recalled Item: Radiometer Recalled by Radiometer Medical ApS Due to Arterial Blood Sampler...

The Issue: Arterial Blood Sampler sterility cannot be guaranteed throughout the shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2022· Instrumentation Laboratory

Recalled Item: HemosIL ReadiPlasTin Recalled by Instrumentation Laboratory Due to Variable...

The Issue: Variable and out of specification QC results with HemosIL ReadiPlasTin. IL...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2022· Microtek Medical Inc.

Recalled Item: TMJ Arthroscopy Drape Recalled by Microtek Medical Inc. Due to Latex content...

The Issue: Latex content in product was labeled incorrectly as latex free.

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

Class II — Potential Health HazardOngoing
DrugApril 7, 2022· Mylan Pharmaceuticals Inc

Recalled Item: Rifampin for Injection Recalled by Mylan Pharmaceuticals Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 7, 2022· MALVERN PANALYTICAL LTD

Recalled Item: NanoSight NS300 Recalled by MALVERN PANALYTICAL LTD Due to Product found to...

The Issue: Product found to not comply to Class 1 Laser safety requirement.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2022· Synthes (USA) Products LLC

Recalled Item: Radial Head Replacement System Implant is a one-piece Recalled by Synthes...

The Issue: DePuy Synthes Radial Head Replacement System Contraindications added to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2022· MESA BIOTECH, INC

Recalled Item: Accula SARS-CoV-2 Test Recalled by MESA BIOTECH, INC Due to SARS-CoV-2 Test...

The Issue: SARS-CoV-2 Test has an increased potential for false positive results, which...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 6, 2022· Johnson & Johnson Surgical Vision Inc

Recalled Item: TRAY RING COVER Recalled by Johnson & Johnson Surgical Vision Inc Due to...

The Issue: Potential breach in the sterility barrier for tray ring covers.

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

Class II — Potential Health HazardOngoing
DrugApril 5, 2022· North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding

Recalled Item: PT-141 (Bremelanotide Acetate) 10 mg/mL (2 mL) Injection Recalled by North...

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2022· North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding

Recalled Item: ARA-290 (Cibinetide Acetate) 6 mg/mL (4 mL) Injection Recalled by North...

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2022· North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding

Recalled Item: Melanotan II 1 mg/mL (10 mL) Injection Recalled by North American Custom...

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund