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 Sep 3, 2014
Cordis EMPIRA NC RX PTCA Dilatation Catheter
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 3, 2014
McCormick Ground Oregano in 0.75 oz plastic bottle. UPC NUMBER: 52100003566 (as seen on label: 0-523561-6) MCCORMICK…
High riskUsing this product could cause serious injury, illness or death — stop using it now.McCormick & Company, Inc.
FDA (openFDA food enforcement)
Reported Sep 3, 2014
4001PS Neonatal/Paed.Intubation Kit 2.5mm Murphy, LDS 15mm Conn Pediatric Endotracheal Intubation Kit
High riskUsing this product could cause serious injury, illness or death — stop using it now.Smiths Medical ASD, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 3, 2014
The Thermedx Fluid Management System is designed to provide irrigation fluids to irrigate, distend, and debride while…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thermedx LLC
FDA (openFDA device enforcement)
Reported Aug 27, 2014
American Spoon Food Sour Cherry Marmalade, 9.5 oz in glass jars with metal lid e. Total package size (e.g. 12 packages…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Spoon Foods, Inc.
FDA (openFDA food enforcement)
Reported Aug 27, 2014
Gyrus ACMI Falope-Ring Dilator, item 000878-4. The Falope-Ring Dilator is a conical plastic device that is a component…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gyrus Medical, Inc.
FDA (openFDA device enforcement)
Reported Aug 27, 2014
Philips IP5 Information Portal The Expression Information Portal (Model IP5), a display and device controller for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invivo Corporation
FDA (openFDA device enforcement)
Reported Aug 27, 2014
Jody's, Funfetti, Net Wt 7.5 oz (213 g) and 4 oz in clear cellophane bag.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jody's Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 27, 2014
Product is in a 160 gram, light green tin container, labeled in part: "ecoato Sweet Paprika Powder Product of Spain"
High riskUsing this product could cause serious injury, illness or death — stop using it now.The TJX Companies, Inc.
FDA (openFDA food enforcement)
Reported Aug 27, 2014
Gelweave (TM) Vascular Prostheses Manufactured by - VASCUTEK Ltd a TERUMO company
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascutek, Ltd.
FDA (openFDA device enforcement)
Reported Aug 27, 2014
Magna-Fx Cannulated Screw Fixation System Bone Screw Fully Threaded Sterile zimmer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
15 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Esaote PA230E Transducer A portable and cart base ultrasound system for general and cardiovascular imaging
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosound Esaote, Inc.
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Medical Positioning Rapid Response HUT table, Powered Medical Examination table, Model # 1017. Product Usage: Used to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Positioning Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Medtronic Ascenda Intrathecal Catheter models 8780 and 8781, and Ascenda Intrathecal Catheter Pump Segment Revision…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Aug 20, 2014
Vital Sync" VPMP & IM, software, V2.4. (DVD), packaged on a CD or other electronically controlled device. CDs are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nellcor Puritan Bennett Inc. (dba Covidien LP)
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 20, 2014
IntelliSpace Portal (ISP) DX/HX/EX, IntelliSpace Portal (ISP) IX, and IntelliSpace Portal (ISP) LX SPECT IntelliSpace…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Aug 13, 2014
VIDAS TPSA, in vitro diagnostic, for use as an automated quantitative measurement of prostate specific antigen levels…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Aug 13, 2014
Sonopet Ultrasonic Surgical System Console, Ultrasonic Aspirator, Stryker Medtech.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Aug 6, 2014
Patient Data Manager 2.0 (Content manager 2.0, Patient Browser 4.0, DICOM Viewer 2.0) Brainlab Digital Lightbox. A…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Aug 6, 2014
Horizon Medical Imaging It is a medical image and information management application that is intended to receive,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical Immaging
FDA (openFDA device enforcement)
Reported Aug 6, 2014
InTouch Critical Care Bed, Stryker Medical. Model Numbers 2130, 2131, 2140, 2141, 2151, 2152, 2155, and 2156.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
FDA (openFDA device enforcement)
Reported Aug 6, 2014
Emerald Fiberoptic Blade, Macintosh 4, Teleflex Medical. A rigid laryngoscope is a device used to examine and visualize…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 6, 2014
IPM Wound Gel Rx Wound Dressing IPM Wound Gel is indicated for the management of wound healing.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wellspring Pharmaceutical Corporation
FDA (openFDA device enforcement)
Reported Aug 6, 2014
Original Silk Light Soymilk Half Gallon, Distributed by WhiteWave Foods Broomfield, Colorado 80021, UPC 0 25293 60101 7
High riskUsing this product could cause serious injury, illness or death — stop using it now.White Wave Foods, Inc.
FDA (openFDA food 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.