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.

Medical devices

Reported Dec 24, 2025

Myosa for Kids KS1 REF MyOSAKS1_Sb/Sp/Mb/Mp/Lb/Lc KS2 REF MyOSAKS2_Sb/Sc/Mb/Mc/Mp/Lb/Lc Myosa for Kids is a mouthguard…

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

Myofunctional Research Company USA

FDA (openFDA device enforcement)

Meat & poultry

Reported Dec 19, 2025

Maître Saladier Inc. Recalls Lorraine Quiche Products Imported Without Benefit of Import Reinspection

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

Maître Saladier Inc.

USDA FSIS

Medical devices

Reported Dec 17, 2025

Safe-T-Centesis 6 Fr Catheter Drainage Tray, REF: PIG1260T,

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 17, 2025

Bard InLay Optima Size: 6 Fr. x 14 cm, Ureteral Stent Kit REF 787614

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

C.R. Bard Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 17, 2025

Simplot¿ Traditional Reduced Sodium Tater Gems¿ , formed frozen potatoes, 6/5lb bags per case, foodservice item, master…

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

JR Simplot Company

FDA (openFDA food enforcement)

Food

Reported Dec 17, 2025

UPC 8 10248 03165 6 YELLOW Peaches PRODUCE OF U.S.A. NET WT. 4 LBS. MOONLIGHT PACKING CORP. REEDLEY, CALIFORNIA 93654…

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

Moonlight Packing Corporation

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 17, 2025

Brand Name: CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer System Model/Catalog Number:…

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

Orthofix U.S. LLC

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 17, 2025

AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product Description: The AMSCO 7052HP Washer/Disinfector…

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

Steris Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 10, 2025

Hemochron Activated Clotting Time Low-Range Test Cuvette, REF: ACT-LR, to be used with the Hemochron Signature ELITE…

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

Accriva Diagnostics, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 10, 2025

Blonde Beard's Dojo Asian Wing Sauce, wing sauce hot sauce condiment, shelf stable, 2 years, glass bottle, 8 oz, Blonde…

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

Blonde Beard's

FDA (openFDA food enforcement)

Food

Reported Dec 10, 2025

Low-moisture part-skim mozzarella shredded cheese, individually packaged in a plastic bag, as: 1) Always Save -…

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

Great Lakes Cheese Co. Inc.

6 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 10, 2025

Phantom Fibula Nail, 2.8mm x 130mm, Right, Ti, Fibula Nail, REF: P36-128-130R-S

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

Paragon 28, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 10, 2025

Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841,

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

Philips Ultrasound, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 10, 2025

Lava Bun with Green Tea Flavor bright lime green packaging (Frozen) Unsalted butter and cream are listed in the…

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

Prime Food Processing LLC.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Dec 10, 2025

Italian Salad Dressing; Net 1 GAL (3.78L) SKU: 7 67367 00518 4 Creamy Poblano Avocado Ranch Dressing and Dip; Net…

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

Ventura Foods LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Dec 3, 2025

CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K, Description/REF: 25+ TOTALPLUS CP PAK 20K CPM BWV .9 IU/…

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

Alcon Research LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated…

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

Argon Medical Devices, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

CareLink Clinic, REF: MMT-7350

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

Medtronic MiniMed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 3, 2025

1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450

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

Remel, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;

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

Becton Dickinson & Company

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

REF: CC286297 or BS737162 Automated Digital Cell Morphology analyzer DI-60, IVD in conjunction with a Honeywell Vuquest…

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

Cellavision AB

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

Brand Name: Vacuette Product Name: 8 ml CAT Serum Separator Clot Activator Model/Catalog Number: 455071P Product…

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

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

PhD Hemostasis Valve, REF: IN4802/K, IN4802/T, IN4918/A, IN7802/C, IN8802/C, IN9802, IN9802/A, K05-02166B, K05T-02138A,…

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

Merit Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

OC-Auto FOBT-CHEK Negative Controls is the negative hemoglobin control materials designed to monitor FOBT (Fecal Occult…

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

Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC

FDA (openFDA device enforcement)

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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.