Recalls distributed in Louisiana
These notices name Louisiana 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.
3,284 stored notices name Louisiana, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,123 notices were distributed nationwide, so they reach Louisiana too — those are in the archive.
Reported Oct 31, 2012
GE Seno Advantage 1.x, Seno Advantage 2.0, Seno Advantage 2.1 Seno Advantage 1.x, Seno Advantage 2.0, Seno Advantage…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2012
Perfusion System 8000, base 4 pump, 115V safety monitor included The Sarns Modular Perfusion System 8000 is indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 24, 2012
Hemorrhoidal Circular Stapler and Accessories 33mm Product Usage: The PROXIMATE HCS Hemorrhoidal Circular Staplers,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Oct 24, 2012
Licorice Sticks sold under the following brand names: 1) Orange Patch Country Store Licorice Sticks, New Wt, 12 oz.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lehi Valley Trading Co.
FDA (openFDA food enforcement)
Reported Oct 24, 2012
"***PressFT***2.6 w/ Two #1 (4 metric) Hi-Fi***Sutures***NP262***2009-02***CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Linvatec Corp. dba ConMed Linvatec
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 17, 2012
PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
FDA (openFDA device enforcement)
Reported Oct 17, 2012
Battery, 100/115V (Includes charger and connecting cable) The Sarns" Centrifugal System is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
4 more products 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
Optilock 2.7 mm Screw Inserter. Intended Use: The OptiLock Upper Extremity Plating System is intended for fixation of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 10, 2012
MIRS for MATRIX Spine System. Minimally Invasive Reduction Screw (MIRS) for percutaneous instrumentation of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes USA HQ, Inc.
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
DEXIS Imaging Suite - catalog number 1.008.7932, version numbers 10.0.0 through 10.0.3 Radiological Image Processing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Imaging Sciences International, LLC
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
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
The 2.7mm Drilling Guide is a reusable instrument used in conjunction with a drill to prepare oriented holes in bone…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra Life Sci.
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
Guardian II Hemostasis Valve, Model 8210 and Guardian II NC Hemostasis Valve, Model FH102. Intended to maintain…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2012
Zoll X Series Defibrillator/Pacemaker/Monitor Product Usage: The product is used by qualified medical personnel for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ZOLL Medical Corporation
FDA (openFDA device 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 12, 2012
Fresh Mahi Mahi Fillets,10 lb Styrofoam case, labeled in part: "***Mahi Fillets S/ON Costa Rica Wild****KEEP AT 38 OR…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atlantic Fisheries
FDA (openFDA food 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)
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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.