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 Jun 6, 2018
Heinens Organic Nut Mix Net Wt. 9 oz (255g) Distributed By Heinens, Warrensville Hts., OH 44128 UPC 0-36232-01871-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ohio Hickory Harvest Brand Products Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 6, 2018
LINX Reflux Management System, Implant Suture, 12-17 Bead, 0.7T, Product Code LS-xx, sterile, Rx only. Labeled as: a.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Torax Medical, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 6, 2018
Ziyad Brand Tahini, 8oz, 16oz, ¿ gal, 32oz. , packed in glass jars
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ziyad Brothers Importing, Inc.
FDA (openFDA food enforcement)
Reported May 30, 2018
Southwestern Gourmet Butter Popcorn Grand Canyon Foods, Phoenix, AZ
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Grand Canyon Foods International LLC.
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 30, 2018
Sorin Stockert Heater-Cooler System 3T, a) Item #: 16-02-81, 240 v/60 Hz; b) Item #: 16-02-82, 208 v/60 Hz; c) Item #:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 30, 2018
First Step Endoscopic Cleaning Pad, 100ml, Flexible Endoscope Bedside Pre-Clean Kit, Catalogue Number EP-3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Madison Polymeric Engineering
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 30, 2018
Synthes Torque Limiting Handle, Part Number 03.231.013 This device is used in systems indicated for fracture fixation.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported May 23, 2018
Thoratec HeartMate 3 LVAS Implant Kit, Rx Only, Catalog # 106524US, 106524, 10652INT - LVAS KIT, HM 3 Indicated for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abbott
FDA (openFDA device enforcement)
Reported May 23, 2018
DIABEATIC Chocolate Berry Crunch bar NET WT 1.4 oz (42g)Manufactured and Distributed by eBars, LLC, Franklin, TN 37064…
High riskUsing this product could cause serious injury, illness or death — stop using it now.eBars
12 more products in this recall
FDA (openFDA food enforcement)
Reported May 23, 2018
Tosoh ST AIA-PACK HbA1c, HbA1c Reagent, Pt. No. 025218 The device is designed for In Vitro Diagnostic Use Only for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 23, 2018
Visaris Vision/Auto, ddRAura OTC APS, Diagnostic X-Ray System, Version 2.2 The Vision systems are intended for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Visaris DOO
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 16, 2018
ARCHITECT DHEA-S Reagent Product Usage: It is a chemiluminescent microparticle immunoassay (CMIA) for the quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
FDA (openFDA device enforcement)
Reported May 16, 2018
BEQ-T 9410 Lurie Chldns Small 1/4, Custom Tubing Kit, Catalog No. 709000430
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Datascope Corporation
27 more products in this recall
FDA (openFDA device enforcement)
Reported May 16, 2018
Humira Pen Sub-q Kit a.) 40 mg/0.8 mL (NDC 00074-4339-02); Humira Pen Psor Kit b.) 40 mg/0.8 mL (NDC 00074-4339-07) 28…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kroger Specialty Pharmacy, Inc.
66 more products in this recall
FDA (openFDA drug enforcement)
Reported May 16, 2018
RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee arthroplasty and knee replacements.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported May 16, 2018
EasyTouch (ET) Insulin Syringe 29G 1ml ¿" (Item 829155) Product Usage: INTENDED FOR INJECTION OF U100 INSULIN ONLY
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MHC Medical Products LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 16, 2018
NeoBase Succinylacetone Assay Solution, Product Number: 3042-0020; Affected UDI Numbers:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PerkinElmer Life and Analytical Sciences, Wallac, OY
FDA (openFDA device enforcement)
Reported May 16, 2018
Sugarfina Platinum Bling Ring; Product SKU No. R-1790 UPC: 840278116139 Net W. 21g ().7 oz.) Sculpted from dark…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sugarfina, LLC
FDA (openFDA food enforcement)
Reported May 16, 2018
Raw Form Organics Maeng Da Kratom Emerald Green; 150 capsule and 300 capsule plastic bottles; Manufactured for Raw Form…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Triangle Pharmanaturals LLC
25 more products in this recall
FDA (openFDA food enforcement)
Reported May 9, 2018
Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision large screen monitor), Interventional fluoroscopic x-ray…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
FDA (openFDA device enforcement)
Reported May 9, 2018
Modular Head Component, Biomet Hip System; Item No. 163669, Hip Joint, metal/polymer semi-constrained cemented…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 2, 2018
EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM, Product Number HEM3335, GTIN Number 1 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 25, 2018
Kratom capsules labeled in the following ways: 1) Divinity Kratom 10 Capsule Dietary Supplement, Divinity Product LLC,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Divinity Product Distribution LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 25, 2018
Cali Green Malay Kratom all packages, all quantities
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nutrizone LLC
9 more products in this recall
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.