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 Jan 16, 2013

Sterile Rigid Tip Suction Wand The Suction Wands are indicated for use to remove excess fluid from the surgical field.

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

California Medical Laboratories Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 16, 2013

Merit Medical's Custom Procedural Tray or Kits K12T-03162B & K12T-02641F.Custom Procedural Tray or Kits is a…

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

Merit Medical Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 16, 2013

Product labeled in part: ***PARAMOUNT RESERVE***PRODUCT OF CHILE FARM RAISED ATLANTIC SALMON PACKED BY: ALIMENTOS…

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

Multiexport Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jan 16, 2013

Emit(R) 2000 Phenobarbital Assay (OSR4D229) and Syva(R) Emit(R) Phenobarbital Assay (4D019UL). Homogeneous enzyme…

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)

Medical devices

Reported Jan 9, 2013

Liko Standard Slingbar 450. The Standard Slingbar 450 is a versatile sling bar which can be used for most lifting…

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

Hill-Rom, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 9, 2013

Medtronic Intersept Custom Tubing Pack with or without coating ( Carmeda BioActive Surfact, Carmeda BioActive Surfact…

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

Medtronic Inc. Cardiac Rhythm Disease Management

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2013

Flowtron Trio DVT Pump; an Rx intermittent pneumatic compression deep vein thrombosis pump; ArjoHuntleigh AB, Eslov,…

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

Arjo, Inc. dba ArjoHuntleigh

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2013

GE Giraffe and Panda T-Piece Resuscitation System labeled ***T-Piece Neonatal Patient Circuit Kit Disposable with Size…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2013

Stryker Howmedica Osteonics; Stryker T2 Humerus System Teflon Tube, sterile; REF 1806-0073S The T2 Nailing System is…

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

Stryker Howmedica Osteonics Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 26, 2012

Arobella Medical 6mm Qurette used with the Arobella Medical AR1000 Wound Therapy System. Major components of the AR1000…

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

Arobella Medical, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 26, 2012

Invacare Height Adjustable (walking) Canes, Model Numbers: 8916, 8917, and 40918-6. The device is packaged six (6)…

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

Invacare Corporation

FDA (openFDA device enforcement)

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)

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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.