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 Oct 17, 2012
Caremor Cliner"***Manufactured By Winco***Ocala, FL 34474 www.wincomfg.com***Model No. 536 Serial No. 536A-101475***"…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Winco Mfg., LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 10, 2012
IR1200, IR1250(IR1200 Plus), 2020 and One Touch(R) Ping(R) Insulin Pump glucose management system. The device is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Animas Corporation
FDA (openFDA device enforcement)
Reported Oct 10, 2012
Endoscopic retrieval device. The disposable Raptor grasping device in intended to retrieve foreign bodies or resected…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.US Endoscopy Group Inc.
FDA (openFDA device enforcement)
Reported Oct 3, 2012
Invacare¿ I-Fit" Shower Chair (Models 9780, 9781, 9781-1), Invacare Corporation, Elyria, OH 44035. These shower chairs…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Oct 3, 2012
Thallous Chloride Tl 201 Injection, Diagnostic Sterile, Non-Pyrogenic Solution, a) 2.8 mL (NDC 0019N12028) b) 6.3ml…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mallinckrodt Inc.
FDA (openFDA drug enforcement)
Reported Oct 3, 2012
Computed Tomography X-Ray Systems, (Brilliance 6, Brilliance 16, MX8000 Dual v. Exp, GEMINI Dual), Philips Healthcare…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Oct 3, 2012
Fruit Mixes: 1) Dining In¿ Super Fruit Medley,10.5oz, UPC 1122508396, Use by date 9/6/2012; 2) Ready Pac¿ Super Fruit…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ready Pac Foods Inc.
11 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 3, 2012
Siemens Magnetom Skyra, Verio, Spectra and Biograph MMR Nuclear Magnetic Resonance Imaging System and Tomographic Imager
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2012
Octopus 101 Perimeter; PeriTrend Software Analysis A perimeter is a device intended to determine the extent of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Haag-Streit USA Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2012
Kimberly-Clark MIC Safety PEG Kit - Pull Type The Kimberly-Clark MIC PEG Kits - Pull type are Percutaneous Endoscopic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kimberly-Clark Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 26, 2012
MX 16-slice CT Scanner System, models 728131 and 728132. The MX 16-slice CT Scanner System can be used as a whole body…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 26, 2012
ProBalance Protein To Go(TM), Milk Chocolate Shake, Dietary Supplement, Net Wt 2.5 fl oz (Responsible firm on labeling:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Protica, Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 19, 2012
Sterile Empty Vial and Injector (30mL PCA vial), Rx only, One/List No. 6021-03, Hospira, Inc., Lake Forest, IL 60045.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hospira, Inc.
FDA (openFDA device enforcement)
Reported Sep 19, 2012
Crown Program BK Fresh Apple Slices, 2 oz On or before August 13; no upc code
High riskUsing this product could cause serious injury, illness or death — stop using it now.Missa Bay, LLC
28 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 19, 2012
Siemens Uroskop Access. Fluoroscopic, image intensified x-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 12, 2012
Nature's Harvest, pine nuts, Net WT 3 oz (85 g), Distributed by Amport Foods, 550 Kasota Ave, SE., Minneapolis, MN…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Importing Co., Inc.
FDA (openFDA food enforcement)
Reported Sep 12, 2012
AmeriWater MRO Dialysis RO+ System, AmeriWater 1303 Stanley Avenue, Dayton, OH 45404 (800) 535-5585 www.AMERIWATER.com.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AmeriWater Inc.
FDA (openFDA device enforcement)
Reported Sep 12, 2012
Fresh Express Hearts of Romaine Crunchy and Sweet 100% Hearts of Romaine Lettuce. 10 oz. plastic bag UPC 71279 26102.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresh Express Incorporated
FDA (openFDA food enforcement)
Reported Sep 12, 2012
syngo(R) Lab Data Manager and syngo(R) Lab Process Manager, all versions. This device is classified as a data…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Sep 12, 2012
100 ft roll of tubing inside a cardboard box. Medical devices are sealed into the tubes prior to ethylene oxide…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Steris Corporation
FDA (openFDA device enforcement)
Reported Sep 5, 2012
Siemens Stratus(R) CS Acute Care(TM) D-dimer Calibrator (DDM CalPak) lots 502058002 and 501318002 The Stratus(R) CS…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2012
UniCel DxH Slidemaker Stainer Instrument System, PN 775222. The DxH Slidemaker Stainer is a fully automated slide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 29, 2012
Hitachi Echelon MRI System/Oasis MRI, Software. These are software controlled MRI devices. Product Usage: The Echelon…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2012
Serial interface module RS-232 Product Usage: The System 1 provides perfusion case data transfer through the use of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
3 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.