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 Mar 22, 2023
Fusion Bioline Vascular Graft, Part number M00201503046B0
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular, LLC
FDA (openFDA device enforcement)
Reported Mar 22, 2023
ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mead Johnson & Company
FDA (openFDA food enforcement)
Reported Mar 15, 2023
Brussel Sprouts 98.5% of product was packaged for retail and 110 cases were bulk Brands: 4 Earth Farms, Trader Joe s,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.4 Earth Farms formerly Mcl Fresh Inc.
FDA (openFDA food enforcement)
Reported Mar 15, 2023
Tri-Staple 2.0 Black Intelligent Reload, Product Number SIG60AXT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LP
FDA (openFDA device enforcement)
Reported Mar 15, 2023
Simplexa COVID-19 Direct, REF: MOL4150; including Reaction Mix, REF: MOL4150; with previous assay definition v2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DiaSorin Molecular LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 15, 2023
Given Imaging SmartBar Cereal Bar; Net Weight 2.53 oz (72 g); Ingredients: glucose syrup, soy crisps, oats, pea…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Given Imaging Ltd.
FDA (openFDA food enforcement)
Reported Mar 15, 2023
Sprint 200 wheeled stretcher, Item numbers 1ES200-7, 1ES210-1, and 1ES211-1.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Linet Spol. S.r.o.
FDA (openFDA device enforcement)
Reported Mar 15, 2023
PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Preat Corp.
FDA (openFDA device enforcement)
Reported Mar 8, 2023
Ultracell Wick with 80cc Collection Bag, 20/box
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beaver Visitec International, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 8, 2023
Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network cards, with IP addresses from x.x.x.224 to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Mar 8, 2023
Summit Medical Nasal Septal Button, Medium, 5cm, REF SP-78105, sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Summit Medical, LLC
FDA (openFDA device enforcement)
Reported Feb 22, 2023
iTotal Identity Impactor Handle, Model No. 1080-212/ED-07827 REV AE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Conformis, Inc.
FDA (openFDA device enforcement)
Reported Feb 15, 2023
The Covera Vascular Covered Stent is a flexible, self-expanding endoprothesis comprised of ePTFE encapsulating a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 15, 2023
TrackX Insight Base Modular Instrument Tracker, 5L, REF #604-3TX, Sterile; and TrackX Insight Base Modular Instrument…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trackx Technology Inc.
FDA (openFDA device enforcement)
Reported Feb 15, 2023
RipCord Syndesmosis Button, REF: STA001K
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TriMed Inc.
FDA (openFDA device enforcement)
Reported Feb 8, 2023
Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter Repair Kit 0601610 4.2 Fr Broviac CV Catheter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 8, 2023
AxiEM" Non-Invasive Patient Tracker
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Feb 8, 2023
SynCardia Total Artificial Heart System (70CC): 500101-001 SynCardia Total Artificial Heart System (50CC): 570500-000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SynCardia Systems LLC
FDA (openFDA device enforcement)
Reported Feb 8, 2023
Turbett Surgical Container, TS1200: Indicated for enclosing other medical devices that are to be sterilized by a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Turbett Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 1, 2023
Parsley bunches Boxes of 30 and 60 count Keep refrigerated SKU 475987 PLU 4899 on twist ties Product of Mexico
High riskUsing this product could cause serious injury, illness or death — stop using it now.Church Brothers, LLC
FDA (openFDA food enforcement)
Reported Feb 1, 2023
Future Diagnostics STAT-IntraOperative-Intact-PTH (STAT-IO-I-PTH) Immunoassay kit REF 4K-IPT-00. in vitro diagnostic.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Future Diagnostics Solutions B.V.
FDA (openFDA device enforcement)
Reported Feb 1, 2023
Revogene SARS-CoV-2_IVD real-time RT-PCR test intended for the qualitative detection of RNA from SARSCoV-2 Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meridian Bioscience Inc.
FDA (openFDA device enforcement)
Reported Feb 1, 2023
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for patients requiring endotracheal intubation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 30, 2023
Wild Cajun Meals LLC Recalls Frozen, Fully Cooked Jambalaya and Gumbo Products Produced without Benefit of Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wild Cajun Meals LLC
USDA FSIS
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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.