All recall categories

Recalls distributed in Mississippi

These notices name Mississippi in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

2,512 stored notices name Mississippi, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Mississippi too — those are in the archive.

Medical devices

Reported Feb 3, 2016

Vantage Panoramic X-Ray System used to perform dental and orthodontic radiological imaging The Vantage Panoramic X-Ray…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Midmark Corp. dba Progeny Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jan 27, 2016

Sulfamethoxazole and Trimethoprim Tablets, USP, 800 mg/160 mg DOUBLE STRENGTH, 100-count bottle, Rx only, Mfg. by:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mutual Pharmaceutical Company, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Jan 20, 2016

AltiVate Reverse Humeral Broach, Size 10 Catalog number 804-06-040, Size 14 Catalog number 804-06-044, and Size 16…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Encore Medical, LP

FDA (openFDA device enforcement)

Medical devices

Reported Jan 20, 2016

UniAxial Pedicle Screw & UniAxial Reduction Pedicle Screw The Response 5.5/6.0 Spine System is intended for…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

OrthoPediatrics Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 13, 2016

Natus Quantum System with NeuroWorks Software. Catalog /Part Numbers: 013926. The Natus Quantum Amplifier is intended…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Natus Neurology dba Excel Tech., Ltd. (XLTEK)

FDA (openFDA device enforcement)

Medical devices

Reported Jan 6, 2016

MOSAIQ Oncology Information System MOSAIQ is an oncology information system used to manage workflows for treatment…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Vancomycin Screen Agar

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Co.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Etest¿ Piperacillin/tazobactam (4 ug/mL) PTc0.016-256-pack of 30 tests WW Etest¿ is a quantitative technique for…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Biomerieux

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

A.L.P.S. 4.0mm Cancellous Locking Screws intended for use in stabilization and fixation of fractures, revision…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Biomet, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Boston Scientific, Chariot ST-CCV Guiding Sheath, Sterilized using ethylene oxide: Product Description Material Number…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

VAPR¿ TRIPOLAR 90" Degree Suction Electrodes (Model/Catalog No: 225028)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

DePuy Mitek, Inc., a Johnson & Johnson Co.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Optional PS500 Power Supply Unit for the Evita V500 Ventilator and Babylog VN500 Ventilator. Babylog VN500 is a…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Draeger Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Reagent Management System (RMS) Dimension EXL with LM Product Usage: The Reagent Management System (RMS) is a module…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 30, 2015

Zimmer UNIVERSAL Power System Loaner and Modular Electric/Battery Double Trigger Handpiece. Rx only Made in Switzerland

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2015

MYLA CLINIC PATCH 3.2.0 CD Product Usage: MYLA is a computer application (Middleware) based on Web 2.0 technology…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

bioMerieux, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 23, 2015

MOSAIQ Oncology Information System. Used to manage workflows for treatment planning and delivery.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Elekta, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Dec 16, 2015

Ventolin HFA (albuterol sulfate) Inhalation Aerosol, 90 mcg per actuation, 200 Metered Inhalations, Rx Only, For Oral…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GlaxoSmithKline, LLC

FDA (openFDA drug enforcement)

Medical devices

Reported Dec 16, 2015

Olympus ENDOEYE HD II Video Telescopes. Models WA50040A ENDOEYE HD II, 10 mm, 0 degree, WA50042A ENDOEYE HD II 10 mm,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Food

Reported Dec 16, 2015

Kroger 100% natural apple FROM CONCENTRATE 64FL OZ. INGREDIENTS: APPLE JUICE FROM CONCENTRATE (FILTERED WATER, APPLE…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Kroger Co.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 2, 2015

Dimension Vista System (MG) ; Flex reagent cartridge Catalog number K3057, SMN 10445158. For the quantitative…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 25, 2015

Herr's Sour Cream & Onion Flavored Potato Chips

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Herrs Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 25, 2015

Hill-Rom 100 Low Bed (GPAC) AC Powered adjustable hospital bed

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hill-Rom, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 25, 2015

Mountain Mix 2oz bag, 7oz pouch, 10oz pouch, 17oz tin, 28oz pouch & 25lb bag. INGREDIENTS: Raisins, Peanuts (Peanuts,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Kanan Enterprises, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Nov 25, 2015

Kar's Sweet n' Salty Mix Box of 18, 3.5 oz. flexible film bags. 1 box per case.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Kar Nut Products Company

10 more products in this recall

FDA (openFDA food enforcement)

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Other states

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.