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 Jan 22, 2014
pO2 D999 membrane units. Distributed by Radiometer America, Inc., Westlake, OH 44145 pO2 membrane units, ordering…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2014
Oxoid Antimicrobial Susceptibility Testing Disc, MEM10, REF: CT0774B, 10 mcg meropenem, Packed in packs containing 5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
FDA (openFDA device enforcement)
Reported Jan 15, 2014
Sandel Healthcare Safety Devices Weighted Safety Scalpel #3 Disposable Safety Handle with #10 Blade Manufactured for:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ansell Sandel Medical Industries LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 15, 2014
SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed As GE Healthcare CARESCAPE Patient Data Module)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jan 15, 2014
Jelco Smiths Medical Hypodermic Needle-Pro¿ Fixed Needle Insulin Syringe, 1.0ml 29g x 1/2 in Reference: 4429-1…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 8, 2014
Diet Coke, 2L, 67.6 FL OZ (2 QT 3.6 FL OZ), UPC 4900005011
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coca Cola Bottling Company United-East, LLC
FDA (openFDA food enforcement)
Reported Jan 8, 2014
VERIFY¿ Dual Species Self-Contained Biological Indicator, Distributed by STERIS Corporation, Mentor, OH. Intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2014
Self-Rising White Cornmeal Mix sold under the Aunt Jemima brand and packaged in a paper bag with a net weight…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quaker Foods and Snacks North America
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 1, 2014
Macaroni Reg CAD, Formula MA.50, Macaroni Salad, packaged: -7-Eleven Fresh to Go Macaroni Salad, 12/7-oz carton cases.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Reser's Fine Foods, Inc.
212 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 1, 2014
Ziehm Vista/Vista Plus C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imaging
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ziehm Imaging Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2013
Continuous Peripheral Nerve Block Catheter Kit and Set Continuous Peripheral Nerve Block Catheter Kit and Set permits…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device enforcement)
Reported Dec 25, 2013
VITROS CA 125 II Calibrators For use in the calibration of the VITROS ECi/ECiQ Immunodiagnostic Systems, VITROS 3600…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported Dec 25, 2013
Oxoid Antimicrobial Susceptibility Test Discs, CTO425B Ciprofloxacin CIP 5 mcg, 50 discs per cartridge, 5 cartridges…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Remel Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2013
Dimension(R) TACR Flex(R) reagent cartridge (DF107) The TACR method is an in vitro diagnostic test intended to…
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)
Reported Dec 25, 2013
Medfusion¿ 4000 Syringe Infusion Pumps Medfusion¿ 4000 Syringe Infusion Pumps are designed for use in care areas for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
FDA (openFDA device enforcement)
Reported Dec 11, 2013
Crunch Pak Apple Slices with Low Fat Caramel Dip, 5/2.5 oz. Tart with Caramel Sauce. The clamshell includes 5/2 oz.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Crunch Pak, LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 11, 2013
17-P 1ml, Main Street Compounding Pharmacy, 126 East Main Street, Newbern, TN 38059, 888-658-6200
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Main Street Family Pharmacy, LLC
298 more products in this recall
FDA (openFDA drug enforcement)
Reported Dec 4, 2013
Mozzarella String Cheese made with 2% milk for 1/4 less fat, sold under Kraft brand or Polly-O brand and packaged with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kraft Foods Group
7 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 27, 2013
GE Healthcare Discovery NMCT 670, Discovery NM 630, Optima NMCT 640, & Brivo NM 615. The GE Discovery NMJCT 670 system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2013
The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hospira Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2013
Cougar¿ Nitinol Workhorse Guidewire: Models: CGRLS190HJ, CGRLS190HS, CGRLS190S, CGRLS300HS, CGRLS300S. CGRXT190HJ,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Vascular
7 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2013
VITROS Chemistry Products ACET Slides, 90 slides/pack; catalog number 1037274 VITROS Chemistry Products ACET Slides…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
36 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2013
Salter Labs EtCO2 Sample line 15' (4.6 M) tube, male luer connectors. Rx only; Made in Mexico; Manufacturer:Salter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Salter Labs
FDA (openFDA device enforcement)
Reported Nov 20, 2013
SIGMA SPECTRUM Infusion Pump with Master Drug Library component (SHARP LCD screen, 55074-2 revision B) Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corp.
1 more product 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.