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 Jun 27, 2018

Kellogg's Honey Smacks, 15.3 oz. and 23 oz.

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

Kellogg Company

FDA (openFDA food enforcement)

Medical devices

Reported Jun 27, 2018

Nitinol Staple, Elastic Staple Large-Asymmetrical, Sterile R, Model #: a) ES-18x15x17; b) ES-18x17x19

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

TriMed Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 20, 2018

XCELA PASV 5F SL 55CM IR-145 Nitinol Wire KIT PG, Catalog Number 25-124

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

Angiodynamics Inc. (Navilyst Medical Inc.)

37 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 20, 2018

Snak Club Tropical Trail Mix: 16 oz. plastic pouch: Ingredients: Raisins, Peanuts, Pineapple, Papaya, Banana Chips,…

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

New Century Snacks LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jun 20, 2018

IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865350

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

Philips Electronics North America Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 13, 2018

Draeger Jaundice Meter JM-103 The device is intended for use in hospitals, clinics or doctor s offices under a…

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

Draeger Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 13, 2018

NaturaLyte¿ Liquid Acid Concentrate for Bicarbonate Dialysis, 3.43 Liters, Part Number: 08-3231-1 Product Usage: This…

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

Fresenius Medical Care Renal Therapies Group, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 13, 2018

Centricity PACS-IW with Universal Viewer Product Usage: Usage: Centricity PACS-IW with Universal Viewer is a device…

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

GE Healthcare

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Jun 13, 2018

Valsartan Tablets USP, 320 mg, 90 tablet, Rx Only, Manufactured by: Jubilant Generics Ltd. Roorkee - 247661, India,…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Jubilant Cadista Pharmaceuticals, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Jun 13, 2018

ADVIA Centaur BNP (B-type Natriuretic Peptide), Catalog Numbers: 02816138 (100 tests), 02816634 (500 tests)

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

Siemens Healthcare Diagnostics, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 6, 2018

Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators, Catalog No C650-129A (00821925008700) The cord consists…

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

Gyrus Acmi, Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Jun 6, 2018

CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP), Part Number 0998-00-0800-XX & 0998-UC-0800-XX (excluding…

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

Maquet Datascope Corp. - Cardiac Assist Division

FDA (openFDA device enforcement)

Medical devices

Reported Jun 6, 2018

LINX Reflux Management System, Implant Suture, 12-17 Bead, 0.7T, Product Code LS-xx, sterile, Rx only. Labeled as: a.…

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

Torax Medical, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 30, 2018

Edwards Lifesciences' IntraClude Intra-Aortic Occlusion Device. Packaged in a sterile barrier system. Model Number:…

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 30, 2018

Sorin Stockert Heater-Cooler System 3T, a) Item #: 16-02-81, 240 v/60 Hz; b) Item #: 16-02-82, 208 v/60 Hz; c) Item #:…

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

LivaNova USA

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 30, 2018

First Step Endoscopic Cleaning Pad, 100ml, Flexible Endoscope Bedside Pre-Clean Kit, Catalogue Number EP-3

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

Madison Polymeric Engineering

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 30, 2018

Hilltop Hearth Self-Rising Flour, Katy s Kitchen Self-Rising Flour, Springwell A1 Flour all packaged in 50 pound paper…

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

Shawnee Milling Company, Inc.

FDA (openFDA food enforcement)

Food

Reported May 23, 2018

DIABEATIC Chocolate Berry Crunch bar NET WT 1.4 oz (42g)Manufactured and Distributed by eBars, LLC, Franklin, TN 37064…

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

eBars

12 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 23, 2018

Visaris Vision/Auto, ddRAura OTC APS, Diagnostic X-Ray System, Version 2.2 The Vision systems are intended for use in…

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

Visaris DOO

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 16, 2018

ARCHITECT DHEA-S Reagent Product Usage: It is a chemiluminescent microparticle immunoassay (CMIA) for the quantitative…

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

Abbott GmbH & Co. KG

FDA (openFDA device enforcement)

Medical devices

Reported May 16, 2018

Fabius MRI, anesthesia machine, catalog no. 8607300 Product Usage: The products are inhalation anesthesia machines for…

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

Draeger Medical, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported May 16, 2018

Humira Pen Sub-q Kit a.) 40 mg/0.8 mL (NDC 00074-4339-02); Humira Pen Psor Kit b.) 40 mg/0.8 mL (NDC 00074-4339-07) 28…

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

Kroger Specialty Pharmacy, Inc.

66 more products in this recall

FDA (openFDA drug enforcement)

Medical devices

Reported May 16, 2018

EasyTouch (ET) Insulin Syringe 29G 1ml ¿" (Item 829155) Product Usage: INTENDED FOR INJECTION OF U100 INSULIN ONLY

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

MHC Medical Products LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported May 16, 2018

Munk Pack PROTEIN COOKIE DOUBLE DARK CHOCOLATE NET WT 2.96oz (84g); UPC: 853787005368

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

Munk Pack Inc.

1 more product 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.