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.
Reported Apr 30, 2014
ZYM B Reagent (REF 70493). The ZYM B reagent is an additional test used to reveal the results of some miniaturized…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 30, 2014
RaySearch Ray Station Radiation Therapy Treatment Planning System, Stand-alone software. Versions 2.0, 2.5, 3.0, 3.5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Apr 30, 2014
Stryker PenAdapt"; Rx Only, Sterile. This device is an accessory to an electrosurgical unit (ESU). The PenAdapt is used…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Apr 16, 2014
400003 Medcare Lift with Scale 400013 Medcare Lift w/Scale 600 lb 400600 Scale Hanger Assembly Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ErgoSafe Product LLC dba Prism Medical Services
FDA (openFDA device enforcement)
Reported Apr 9, 2014
3M" Steri-Vac" Gas Sterilizer/Aerators, Model #'s 4XL,5XL, 8XL The 3M" Steri-Vac" Gas Sterilizer/Aerator is a compact…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Company - Health Care Business
FDA (openFDA device enforcement)
Reported Apr 9, 2014
Proceed Surgical Mesh, Product Codes PCDB1, PCDT1, and PCDJ1. Ethicon Inc., Johnson & Johnson Medical GmbH, used for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, Inc.
FDA (openFDA device enforcement)
Reported Apr 9, 2014
Ideal Protein Double Chocolate Brownie. Individually wrapped, sold in boxes of 7.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Laboratories Cop Inc.
FDA (openFDA food enforcement)
Reported Apr 9, 2014
Pinnacle3 Radiation Therapy Planning (RTP) System, software version 9.0.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland), Inc.
FDA (openFDA device enforcement)
Reported Apr 9, 2014
RayStation Radiation Therapy Treatment Planning System, models 2.5, 3.0, 3.5 and 4.0; a software system designed for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 9, 2014
Weck Vista Universal Laparoscopic Port, Size 5/10mm x 100mm, Catalog No. 405910, Weck Vista Universal Laparoscopic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 2, 2014
HeartMate II Implant Kit with Pocket Controller; with sealed grafts (NAm) with sealed grafts (EU) Product Usage:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Thoratec Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 2, 2014
DICOM Export Format for Sum Dose with Velocity v3.0.0. A stand-alone software product that provides the oncology care…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Velocity Medical Solutions, LLC
FDA (openFDA device enforcement)
Reported Mar 26, 2014
Halogen Lamp component in RetCam 3 System - Clarity Medical Systems, Inc; Pleasanton, CA. General ophthalmic imaging…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Clarity Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Mar 26, 2014
Philips HeartStart FR3 Automated External Defibrillator (AED), models 861388 and 861389. The HeartStart FR3 is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems North America Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 26, 2014
Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube set is indicated for uses commonly associated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Mar 26, 2014
Gender Solutions" Natural-Knee¿ Flex System: N-K FLEX MBACK SZ 0 PAT N-K FLEX MBACK SZ 1 PAT N-K FLEX MBACK SZ 2 PAT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
14 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 19, 2014
Navigator Surgical Kit Product Usage: Molded plastic tray used in holding various dental instruments for autoclave…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet 3i, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 19, 2014
RetCam 3, RetCam Portable and RetCam Shuttle; manufactured by Clarity Medical Systems, Inc.; Pleasanton, CA 94588.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Clarity Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Mar 19, 2014
XiO RPT System The XiO RTP System is used to create treatment plans for any cancer patient for whom external beam…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Mar 19, 2014
GE Healthcare, Innova 2100IQ, Innova 3100, Innova 3100IQ, Innova 4100, Innova 4100IQ Innova 2121IQ, Innova 3131IQ;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 19, 2014
HER2 Image Analysis Manual Read of HER2 Digital Slides ER/PR Image Analysis IHC PR Breast Tissue Manual Read of Digital…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Biosystems Imaging, Inc.
FDA (openFDA device enforcement)
Reported Mar 19, 2014
Smith & Nephew RENASYS Soft Port REF: 66800799 (The RENASYS Soft Port Dressing Kits are used in conjunction with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 19, 2014
4040-2: Umbilical 3 mL Line Draw, Luer lock syringe (heparin concentration: 23.5 I.U. per mL) with Filter-Pro¿ device,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 12, 2014
All Elekta digital accelerators with electrons and beam modulator, MLCi/MLCi2, Agility or Asymmetric Heads Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
5 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.