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 Aug 16, 2017
iGUIDE Software 2.2 Product Usage: Control of accurate patient positioning with assistance of a 30 Tracking System in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Aug 16, 2017
Syringe Bulb, 60 CC 50 pcs per case. The products are used to inject fluids into, or withdraw fluids from the body.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.International Medsurg Connection, Inc.
58 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 9, 2017
Professional Formulas Sublinqual B12 High-Potency dietary supplement, 60-count dissolvable tablet in white plastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Professional Complementary Health Formulas, LLC
FDA (openFDA food enforcement)
Reported Aug 9, 2017
InflammaDry(R) AN RPS DIAGNOSTIC SOLUTION, Sample Collectors InflammaDry(R) is a rapid, immunoassay test for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quidel Corporation
FDA (openFDA device enforcement)
Reported Aug 9, 2017
SoftLab Software Laboratory information system to be used in a medical research or clinical laboratory by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Soft Computer Consultants, Inc.
FDA (openFDA device enforcement)
Reported Aug 9, 2017
Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid Exchange Catheters Device is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectranetics Corporation
FDA (openFDA device enforcement)
Reported Aug 9, 2017
Lactulose Solution, USP, 10 g/15 mL, dose cups delivers 15 mL packaged in 50-unit dose cups per case, Manufactured by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.VistaPharm, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Aug 2, 2017
BioHealth Pasture Fed Precision Blend Time Release Protein: Cookies and Cream Flavor; Sold in 2 lb.(960G) UPC 6 42014…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Innovative Nutrition Technologies
FDA (openFDA food enforcement)
Reported Aug 2, 2017
STOCKERT Heater-Cooler System 3T, 230 V
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group USA, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 26, 2017
Agfa Healthcare NX 3.0.8950 Imaging Processing Software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AGFA Healthcare Corp.
FDA (openFDA device enforcement)
Reported Jul 26, 2017
MAKO RIO Standard System, internal cPCI Card CageP/N: 201337. Intended to assist the surgeon in providing software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Beckman Coulter Synchron AQUA CAL Level 1, Part No. 471288 Product Usage: Used for the system calibration of Na, K, Cl,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Jul 19, 2017
On-X Prosthetic Heart Valve Product Usage: Indicated for the replacement of diseased, damaged, or malfunctioning native…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CryoLife, Inc.
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Carestation 620 A1, Carestation 650 A1, and Carestation 650c A1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Simple truth Dry Roasted Macadamia Nuts 12 oz bags UPC 0 1111 00247 8 DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kroger Corporate Food Technology Laboratory
FDA (openFDA food enforcement)
Reported Jul 19, 2017
The Olympic Pasteurmatic 3000 and Olympic Pasteurmatic 3500 are intended for cleaning and high-level disinfection of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Medical Incorporated
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Nicolet¿ Elite¿ 2 MHz OB Probe, Non-Fetal Monitor, Model #: X1L007, Catalog Code: N200. Intended for non-invasive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Video Duodenoscope These instruments are intended to provide optical visualization of (via a video monitor), and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pentax
FDA (openFDA device enforcement)
Reported Jul 19, 2017
Potassium PHOSphate added to 250 mL 0.9% Sodium Chloride 10 mMol (14.67 mEq K+) Total Approximate Volume 254 mL, Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SCA Pharmaceuticals
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 12, 2017
Chili Pequino 0.25 oz packaged in a clear plastic bag; Product Code 10106
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bolner's Fiesta Products, Inc.
FDA (openFDA food enforcement)
Reported Jul 12, 2017
Logic Fit Tibial Tamp Head
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 12, 2017
Proteus 235 and Proteus ONE proton therapy systems
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ion Beam Applications S.A.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 12, 2017
Drew Scientific DREW 3-PAC Reagent Kit containing: 5L Diluent, 750 mL Enzymatic Cleaner, and 125 mL Lysing Reagent.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.JAS Diagnostics Inc.
FDA (openFDA device enforcement)
Reported Jul 12, 2017
Nussloch GmbH ASP6025 Tissue Processor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Louisiana recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
Other states
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.