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.

2,477 stored notices name Mississippi, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Mississippi too — those are in the archive.

Food

Reported Feb 13, 2019

Gold Medal Unbleached All Purpose Flour. Net Wt 5 lb. (2.26kg). UPC 16000-19610. Distributed By General Mills Sales,…

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

General Mills, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 13, 2019

Henry Schein CU 1000 Halogen Curing Light, Catalog 900-4542. - Product Usage: Curing light for use in dentistry. The…

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

Handpiece Headquarters

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2019

Portex 350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿

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

Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

12 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Feb 10, 2019

VICS Acquisition, LLC retira productos de pollo debido a un error de rotulación y alérgenos no declarados

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

VICS Acquisition, LLC

USDA FSIS

Food

Reported Feb 6, 2019

Peaches, sold as a bulk retail item, with PLU 4044, and country of origin of Chile. The peaches sold at Aldi are…

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

Jac Vandenberg Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 6, 2019

Calix Lumbar Spinal Implant System: 22mm x 10mm x 7mm PLIF ASSY PC, REF X034-0172PC 22mm x 10mm x 8mm PLIF ASSY PC, REF…

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

Xtant Medical Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 30, 2019

Del Monte Quality Fresh Cut Harvest Selects Fiesta Corn seasoned with Red & Green Peppers. NET WT 15.25 oz. (432 g);…

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

Del Monte Research Center - Walnut Creek

FDA (openFDA food enforcement)

Medical devices

Reported Jan 30, 2019

Perfusion Pack, Rx only, Sterile EO

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

LivaNova USA

FDA (openFDA device enforcement)

Medical devices

Reported Jan 23, 2019

Arthrex Suture Anchor, Nano Corkscrew FT (consists of an anchor pre-loaded on a handled inserter including suture, with…

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

Arthrex, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 23, 2019

PERMA-HAND Silk Suture Size 5, Black 30" (75cm) Double Armed LR Needles, Product Code 485T Product Usage: PERMA-HAND*…

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

Ethicon, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 23, 2019

U by Kotex¿ Sleek¿, Regular Tampons, 18 Count

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

Kimberly-Clark Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 16, 2019

Various GE Magnetic Resonance System on-site software version Product Usage: Magnetic resonance imaging equipment for…

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

GE Healthcare, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 9, 2019

StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation Cranial Optical Pocket Guide - Instructions for…

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 9, 2019

Enamelast Cool Mint/OT Varnish 5% NaF Mint Label Enamelast Unit Dose 200pk Cool Mint: Enamelast 5% Sodium Fluoride Unit…

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

Ultradent Products, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2019

GEM Coupler Forceps, GEM4183C, packaged individually.

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2019

Thermoset Room Temperature Closed Loop Injectate Delivery System. 1 unit per Cavity #3 Cavity Deep/20 pieces per case…

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

ICU Medical, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2019

Medtronic MiniMed 630G 6025805-003_C, Rx Only Medtronic MiniMed 670G 6025805-005_B, Rx Only Medtronic MiniMed 640G…

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

Medtronic Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2019

RayStation 3.5, RayStation 4.0, RayStation 4.5, RayStation 4.7, RayStation 5, RayStation 6, RayStation 7 and RayStation…

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

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Medical devices

Reported Dec 26, 2018

enVista One Piece Hydrophobic Acrylic Intraocular lens - Is indicated for primary implantation for the visual…

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

Bausch & Lomb Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 26, 2018

VITEK 2 Antimicrobial Susceptibility Testing (AST) using one or more of these susceptibility products: Catalog #…

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

bioMerieux, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 26, 2018

Protexis Neoprene Surgical Glove, Size 5.5 This powder-free sterile light brown colored surgeons gloves are a…

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

Cardinal Health 200, LLC

7 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 26, 2018

Best Taste Brand DRIED BAMBOO SHOOT Mang Non. The product comes in a 12 ounce (340g) uncoded flexible plastic package…

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

Country Favor Inc.

FDA (openFDA food enforcement)

Food

Reported Dec 26, 2018

Milk Chocolate Maltballs: NET Wt. 15 lbs. Item number 992 Case UPC 00797817-00992-9 Allergy Information: This product…

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

Marich Confectionery Company, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 26, 2018

Theragenics Applicator Needle (18g x 20cm) The device is comprised four basic elements; a wire stylus with plastic…

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

Theragenics Corporation

FDA (openFDA device enforcement)

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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.