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 48,122 notices were distributed nationwide, so they reach Mississippi too — those are in the archive.

Food

Reported Dec 19, 2012

Berres Brothers Coffee Roasters Chocolate & Peanut Butter regular whole bean coffee packaged in the following sizes: 12…

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

Berres Brothers, Inc.

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 19, 2012

WANG Transbronchial Aspiration Needles Cat. No. MW-222, WANG Cytology Needles, Central or Peripheral Regions, 22 g x 13…

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

ConMed Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 19, 2012

The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that incorporates a high-resolution color camera, an…

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

Verathon, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 12, 2012

Sara Lee Butter Streusel Coffee Cake, Net Wt. 11.5 oz ; 8 cakes per 5.75 lb case; Distributed by Sara Lee Corp.,…

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

Hillshire Brands Company

FDA (openFDA food enforcement)

Medical devices

Reported Dec 12, 2012

Invivo Corporation Expression MRI Patient Monitoring System. The Expression MRI Patient Monitoring System is intended…

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

Invivo Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 12, 2012

The product has the Catalogue/Part number 60010. Olympic Cool-Cap System is a selective head cooling system for…

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

Natus Medical Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Dec 12, 2012

Dimension Vista(R) IRON Flex(R) reagent cartridge (K3085) The IRON method is an in vitro diagnostic test for the…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 12, 2012

24 Fr 8mm Sft Flow Str Wire W/L The Sarns Aortic Cannula is indicated for use in perfusion of the ascending aorta…

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

Terumo Cardiovascular Systems Corporation

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 5, 2012

Kimberly-Clark Patient Warming System - Model 1000 Control Unit The product is a thermal regulating system, indicated…

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

Kimberly-Clark Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 5, 2012

100/120V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion System 1 is indicated for use for…

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

Terumo Cardiovascular Systems Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2012

"***SENTINEL***Cannulated Drill Bit***S8580***8 X 229mm (9")***CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908…

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

Linvatec Corp. dba ConMed Linvatec

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2012

The RIO (TGS 2.), Model # MAKO TGS 2.0 (Part No. 204000). The RIO is intended to assist the surgeon in providing…

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

Mako Surgical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2012

Dimension Vista(R) Systems Vista(R) Theophylline THEO Flex(R) Regent Cartridge (K4071) The THEO method is an in vitro…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 28, 2012

Styker Orthobiologics Vita Plasma Separator, a component of Vitagel Surgical Hemostat. Sterile, single use device…

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

Stryker Orthobiologics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 14, 2012

Boule Con-Diff Hematology Control For in vitro diagnostic use as a control to monitor the performance of…

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

Clinical Diagnostic Solutions

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 14, 2012

S5 Single Roller Pump 150, Item Number: 10-80-00 The Stockert S5/Sorin C5 System is intended to be used during…

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

Sorin Group USA, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 14, 2012

The Nut Shop (brand) Roasted Peanuts, 3.0 oz MIN Wt.

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

Williams and Company Inc. dba The Nut Shop

FDA (openFDA food enforcement)

Food

Reported Oct 31, 2012

Kraft Jalapeno String Cheese, Net Wt 12 Oz (340 g); a natural low-moisture part-skim mozzarella cheese with jalapeno…

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

Kraft Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 31, 2012

Gish 3/8 x 3/8" Straight Connector with Luer fitting, Item Numbers: EC2160B, EC2160S, Lot Numbers: 1210100010,…

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

Sorin Group USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 31, 2012

Perfusion System 8000, base 4 pump, 115V safety monitor included The Sarns Modular Perfusion System 8000 is indicated…

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

Terumo Cardiovascular Systems Corporation

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 24, 2012

Hemorrhoidal Circular Stapler and Accessories 33mm Product Usage: The PROXIMATE HCS Hemorrhoidal Circular Staplers,…

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

Ethicon Endo-Surgery Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 17, 2012

3M Steri-Vac Gas Sterilizer/Aerator models 5XL and 8XL. 3M Steri-Vac Gas Sterilizer/Aerator is a compact unit designed…

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

3M Company - Health Care Business

FDA (openFDA device enforcement)

Medical devices

Reported Oct 17, 2012

Emit(R) 2000 Phenobarbital Assay (OSR4D229) and Syva(R) Emit(R) Phenobarbital Assay (4D019UL) Product Usage: Enzyme n…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 17, 2012

Battery, 100/115V (Includes charger and connecting cable) The Sarns" Centrifugal System is indicated for use in…

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

Terumo Cardiovascular Systems Corporation

4 more products in this recall

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.