All recall categories

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.

Food

Reported Aug 4, 2021

Del Monte Fresh Cut Golden Sweet Whole Kernel Corn; 15.25 oz. can (24 x 15.25 oz. cans per case) Case UPC …

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Del Monte Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 4, 2021

OEC 3D Imaging, Image-Intensified Fluoroscopic X-Ray System, Mobile - Product Usage: designed to provide fluoroscopic…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE OEC Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 4, 2021

basixALPHA Inflation Device 30 atm/bar 20 mL - Product Usage: Used to inflate and deflate an angioplasty balloon or…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Merit Medical Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 4, 2021

Now Real Food Organic Steel Cut Oats, 2 lb bag, code 6295, UPC 733739062956, packed 8 bags per case; case packaging is…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

NOW Health Group Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 4, 2021

ThermoScientific Oxoid Antimicrobial Susceptibility Discs Rx only Made in the United Kingdom

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Remel Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 4, 2021

Zippie Voyage, early intervention stroller - Product Usage: is manually operated by a caregiver for purposes of…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sunrise Medical (US) LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 28, 2021

Suture Anchor, BioComposite SwiveLock C, 5.5 mm x 19.1 mm, Closed Eyelet, REF AR-2323BCC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Arthrex, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 28, 2021

Infant Heel Warmer with Attachment Tab, Nonsterile, Active Product SKU MH00002T The infant heel warmer is activated at…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cardinal Health 200, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 28, 2021

DJO Surgical EMPOWR 3D Knee Tibial Insert - e-plus, REF: 341-12-711, Left Sz. 11 12mm, CE0086, Sterile H2O2, UDI:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Encore Medical, LP

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 28, 2021

Philips Respironics V60 Ventilator with Software Versions 3.00 and 3.10. The Respironics V60/V60 Plus Ventilator is an…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Respironics California, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 21, 2021

Toshiba Vantage Tiitan 1.5T with Standard gradient, Premium Open-Bore MRI System, REF: MRT-1504 - Product Usage: use as…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Canon Medical System, USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 21, 2021

Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Sterile EO Rx Only

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

FDA (openFDA device enforcement)

Medical devices

Reported Jul 21, 2021

Lingen Disposable Virus Sampling Kit, Item MTM-04, 40 tubes/box.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mercedes Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 14, 2021

Beech-Nut brand Single Grain Rice Baby Cereal; NET WT. 8 OZ (227g); INGREDIENTS: Rice flour, sunflower lecithin;…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beechnut Nutrition

FDA (openFDA food enforcement)

Medical devices

Reported Jul 14, 2021

FilmArray Pneumonia Panel (Pneumo) Part Numbers: Part No: RFIT-ASY-0144 / UDI: 00815381020178 (30 test kit) Part No:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioFire Diagnostics, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 14, 2021

Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) Model Number: 20-006-024

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Luminex Corporation

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 14, 2021

CoreValve Evolut R Delivery Catheter System, REF: ENVEOR-L; ENVEOR-N;

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Heart Valves Division

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 7, 2021

Edwards TruWave (3 cc)/VAMP Jr 48 in (120 cm) Kit, REF: PXVJ356, Pressure Monitoring Set, RX Only, CE, Sterile EO,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Edwards Lifesciences, LLC

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 7, 2021

Continuous CT Fluoroscopy DVI Ceiling Mount CCT Arm DVI Option - Monitor Bracket Assembly for use with CT and PET/CT…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips North America LLC

11 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 7, 2021

Synaptive Trackable Suction Set Standard and Malleable

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Synaptive Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 30, 2021

Access SARS CoV-2 lgG II Reagent, REF: C69057, IVD CE UDI: (01)15099590742744

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 30, 2021

inLight Medical LED Pads used with Polychromatic light technology system

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Inlightened Partners LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 30, 2021

Medical Action INDUSTRIES INC., Disposable Instrument Pack Mosquito Hemostat, REF 56220

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medical Action Industries, Inc. 306

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 30, 2021

GENOSYL DS; Nitric Oxide Delivery System Combination Product NDA202860

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Vero Biotech, LLC

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.

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.