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 Jul 31, 2024

ABL800 FLEX Model Numbers 393-800 and 393-801 The ABL800 FLEX analyzers are intended for: " In Vitro testing of samples…

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2024

Abbott Proclaim XR 5 Implantable Pulse Generator, REF 3660, Sterile EO, Rx Only

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

Abbott Medical

11 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2024

Surgical Image Guidance Functionality, software used with NGENUITY 3D Visualization System, Part Number: 8065000399

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

Alcon Research LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2024

BD Multitest 6-Color TBNK CE-IVD, REF: 644611; BD Multitest 6-Color TBNK Kit with BD Trucount Tubes CE-IVD, REF:…

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

Becton, Dickinson and Company, BD Biosciences

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2024

BD Pyxis: MedStation ES (Main), REF: 323; MedStation ES Tower, REF: 352; Anesthesia Station ES, REF: 327; CII Safe ES,…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 24, 2024

VACUETTE¿ TUBE 8 ml CAT Serum Separator Clot Activator 16x100 red cap-yellow ring, non-ridged

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

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 17, 2024

C. Kreuger Gluten Free White Chocolate Cherry Oatmeal Cookies, 2oz in plastic sleeve. 60 cookies per case. Storage for…

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

C. Krueger Finest Baked Goods

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 17, 2024

Kosmos on iOS impacting iOS, Model Numbers: P007639, P007944, software is part of a general-purpose diagnostic…

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

Echonous Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 10, 2024

Abbott Liberta RC, Implantable Pulse Generator, REF: 62400, STERILE, RxONLY

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

Abbott Medical

FDA (openFDA device enforcement)

Medical devices

Reported Jul 10, 2024

AMT Initial Placement Dilator Set. Used to place gastrostomy devices.

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

Applied Medical Technology Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 10, 2024

BD Pyxis, Name/REF: MEDBANK MINI 1FH-1FM/ 169-137, MEDBANK MINI 1FH-2HH MEDPASS/ 169-151, MEDBANK MINI 1HH-1FH-1HM/…

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

CareFusion 303, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 10, 2024

First Source Vision M. Portable cart and platform that supports an X-ray system and laptop computer.

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

First Source Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 10, 2024

Drug Emporium Yogurt Flavored Pretzels, 8oz (227g) , GNS Foods, Arlington, TX 76011

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

GNS Foods, Inc.

FDA (openFDA food enforcement)

Food

Reported Jul 10, 2024

Walmart Great Value Organic Black Chia Seeds 32 oz.

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

Natural Sourcing International,LLC

FDA (openFDA food enforcement)

Food

Reported Jul 3, 2024

(Item 311) Classic Delight Turkey Ham & Cheese Sub

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

Classic Delight LLC

24 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 3, 2024

Tejocote Root Products under the following brands: Eva Nutrition, Science of Alpha Mexican, NWL Nutra Mexican, and…

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

Global Mix Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 3, 2024

Prelude Roadster Guide Sheath REF: -PG4F45S -PG4F90S -PG5F45MP -PG5F45R -PG5F45S -PG5F45S018 -PG5F90MP -PG5F90S…

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

Merit Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 3, 2024

Software version 5.3 in: RAPIDPoint 500e Blood Gas System (USA) Siemens Material Number: 11416751 RAPIDPoint 500e Blood…

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

Siemens Healthcare Diagnostics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 3, 2024

2nd Generation CentriMag Primary Console, REF: 201-90401, 201-90701, 201-90411, 201-90421, 201-30300, L201-90401,…

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

Thoratec Switzerland GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Jun 26, 2024

TabloCart with Prefiltration Drawer PN-0006813, with power cords: PN-0005746 (10-foot), PN-0006578 (15-foot),…

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

Outset Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 19, 2024

MRI systems: Vantage Orian MRT-1550 (MEXL-1550), Vantage Elan MRT-2020 (MEXL-1520), Vantage Titan MRT-1504 (MEXL-1504),…

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

Canon Medical System, USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 19, 2024

EsoFLIP, 30mm BALLOON DILATION CATHETER, REF ES-330, Rx Only

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

Covidien, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 19, 2024

MyoSPECT System, Model H3912AA and H3912B, and MyoSPECT ES System, Model H3912AB and H3912BD, dedicated cardiac SPECT…

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

Ge Medical Systems Israel, Functional Imaging

FDA (openFDA device enforcement)

Food

Reported Jun 19, 2024

Grande Lactose SKU 30600. Grade A. Refined Pasteurized. Net Wt 25 kg. Ingredients: Lactose Contains Milk. Grande Custom…

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

Grande Cheese Company

10 more products in this recall

FDA (openFDA food 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.