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 48,100 notices were distributed nationwide, so they reach Louisiana too — those are in the archive.
Reported May 18, 2022
Bwell Bird's Nest Beverage Pandan Flavor NET 8.45 FL OZ (250mL) UPC 8373726342 24 bottles per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eastland Food Corporation
5 more products in this recall
FDA (openFDA food enforcement)
Reported May 18, 2022
11001RD1 11001RDK1 KARL STORZ Slim Nasopharyngolaryngoscope 96216006US V5.0 (10-2018)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
11 more products in this recall
FDA (openFDA device enforcement)
Reported May 18, 2022
Kill 'Dat Sanitizing Products Hand Sanitizer, 1 gallon (128 fl. oz.) 80% Alcohol, OTC, Manufactured by: Lula Holdings…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lula Holdings LLC
FDA (openFDA drug enforcement)
Reported May 18, 2022
Medtronic IN.PACT Admiral, Paclitaxel-coated PTA Balloon Catheter, Sterile EO, Rx Only for the following model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Vascular, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 18, 2022
OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product, Product code MG412143
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Simplivia Healthcare Ltd.
FDA (openFDA device enforcement)
Reported May 11, 2022
K-Wire, 1.35 mm x 170 mm
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported May 4, 2022
ZEISS miLOOP Lens Fragmentation Device REF 303071-9090-000. Used during cataract surgery.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Meditec AG
FDA (openFDA device enforcement)
Reported May 4, 2022
Drager Infinity CentralStation Software versions VG2.1.2 and VG2.1.2 SU12. For patient monitoring with Infinity M300…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draegar Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported May 4, 2022
da Vinici X da Vinci Xi Sureform 45 REF 480445 da Vinci X da Vinci Xi Sureform 45 Curved-Tip REF 480545 da Vinici X da…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported May 4, 2022
MEDTRONIC INTERSTIM THERAPY SYSTEM FOR URINARY CONTROL, which includes the following: a) Handset with Communicator,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported May 4, 2022
TearCare version 1.0 SmartHubs
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sight Sciences, Inc.
FDA (openFDA device enforcement)
Reported May 4, 2022
Organic Marketside Zucchini 2 Count packages/8 per case Ingredients: Organic Zucchini New WT. 6 oz. (170g) UPC:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.World Variety Produce Inc. dba Melissa's
FDA (openFDA food enforcement)
Reported Apr 27, 2022
4.0mm x 10mm Cannulated Screw, Short Thread; Part number 3005-40010
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 27, 2022
ORAcollect Dx, Catalog Number/SKU: OCD-100, OCD-100A. Material numbers: OCD-100, OCD-100.008, OCD-100.012,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DNA Genotek Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 27, 2022
Matrix Clinical Solution At-Home COVID-19 Test
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Matrix Medical Network
FDA (openFDA device enforcement)
Reported Apr 27, 2022
Philips Respironics V60 Ventilator (All Models, including: 1053613, 1053614, 1053615, 1053616, 1053617, 1053618,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Respironics California, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 27, 2022
Merlin PCS 3650 programmer Model 3330 software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St. Jude Medical, Cardiac Rhythm Management Division
4 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2022
20/30 INDEFLATOR -REF 1000184 WPL2122268-01 (2019-03-01)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Vascular
4 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2022
Verigene Processor SP, Model Numbers: 10-0000-07 and 10-0000-07-R
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
FDA (openFDA device enforcement)
Reported Apr 20, 2022
Hydroxybutyrate LiquiColor Tests - includes 3 bottles (1 of each size, 3mL, 8.5mL, and 50mL)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2022
Access-9 Large Bore Hemostasis Valves, Catalog Code: 580775001, IN8112/C, K05-00053H, K05-00109G, K05-00137K,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 20, 2022
Cub 2 Enclosed Bed Canopy System
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sensory Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 13, 2022
Ultima Activator II Reusable Drive Mechanism, part # C-UA-5001. Labeled REF UA-5001.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular, LLC
FDA (openFDA device enforcement)
Reported Apr 13, 2022
Caesar dressing in a 1.5 oz pouch
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sauer Brands Inc. - New Century
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.