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 48,122 notices were distributed nationwide, so they reach Louisiana too — those are in the archive.
Reported Mar 22, 2017
Toshiba Kalare DREX-KL80 X-ray generator
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toshiba American Medical Systems Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 15, 2017
Remel, Haemophilus Test Medium (Agar) in A) 100 mm REF R01503, and B) 150 mm plates REF R04033,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
FDA (openFDA device enforcement)
Reported Mar 15, 2017
Color contact lenses labeled under the following brands: Diamond, Fierce, Ambition, Circle Collection, Lunatic, Fright,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The See Clear Company
FDA (openFDA device enforcement)
Reported Mar 15, 2017
Trader Joes Imported English Authentic Lemon Curd, 10.5oz (300g), 24 jars/case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trader Joes Company
FDA (openFDA food enforcement)
Reported Mar 15, 2017
Juno DRF; Model: 709020 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Sistemi Medicali S.P.A.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 8, 2017
BD AffirM VPIII Microbial Identification Test
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Mar 8, 2017
Check-Flo Performer Introducer, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 8, 2017
EliA Sample Diluent, Article number, 83-1023-01
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phadia US Inc.
FDA (openFDA device enforcement)
Reported Mar 8, 2017
PRODISC Orthopedic Manual Surgical Instrument, strut used in spinal surgery. Part numbers 03.820.350 and 03.820.352.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Mar 8, 2017
Abdominoplasty Pack, Part numbers AMS3326(B, AMS4381, and AMS4381(B.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Windstone Medical Packaging, Inc.
123 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 1, 2017
AMT Bridle - Nasal Tube Retaining System Used with Nasogastric/Nasointestinal (NG/NI) tubes.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Applied Medical Technology Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 1, 2017
ETEST XM256 (Cefuroxime), Foam: 506958-506918; SPB: 412304-412305 ETEST is a quantitative technique for determining the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Mar 1, 2017
Oxford Knee System Tibial Resector Body Tube & Guides Product Usage: Instruments for use with the Oxford Uni Partial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet U.K., Ltd.
23 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 1, 2017
DIAMONDBACK 360 Peripheral 1.50 Classic, Model DBP-150CLASS145 Peripheral Orbital Atherectomy System (OAS) is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardiovascular Systems Inc.
FDA (openFDA device enforcement)
Reported Mar 1, 2017
DeRoyal Heart Tracecart REF 53-1769, Rx Only, NON-STERILE PRODUCT CONTAINED WITHIN.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.DeRoyal Industries Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 1, 2017
Golden Flake (R) HOT THIN & CRISPY POTATO CHIPS, NET WT. 5 OZ. (141.8g), Golden Flake Snack Foods, Inc., Birmingham, AL…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Golden Flake Snack Foods Inc.
FDA (openFDA food enforcement)
Reported Mar 1, 2017
A) Palmer's Candies Chocolate Almond Bark , NET WT 9 OZ (255 g) packaged in plastic clamshell container, UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Palmer and Company, dba Palmer Candy Co.
17 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 1, 2017
Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience, Inc.
FDA (openFDA device enforcement)
Reported Mar 1, 2017
GrebSet Micro-Introducer Kit, model 7941, Sterilized with Ethylene Oxide. Product Usage: The GrebSet micro-introducer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Feb 22, 2017
Stryker Restoris RIO Reamer Handle, Offset, Mako Rx only Product Usage: The handle is used to hold surgical components…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Feb 22, 2017
BrightView XCT
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 Feb 22, 2017
LIFEPAK 15 Monitor, Automated External Defibrillator (AED), Manual mode monitoring and therapy functions are intended…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported Feb 22, 2017
CentraLink¿ Data Management System Software Versions: v13x,v14x,v15x The CentraLink system software is a network…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 22, 2017
PICTSWEET(R) FARMS, Southern Classics, Crunchy Breaded Okra, NET WT 12 OZ (340g), UPC 7056098377
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Pictsweet Company
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.