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 Apr 13, 2022

MODEL: X-RAY R/F SYSTEM FLUOROspeed X1

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

Shimadzu Medical Systems

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 13, 2022

BenchMark ULTRA and DISCOVERY ULTRA Instruments

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

Ventana Medical Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 13, 2022

SyncVision Systems, Model: 400-0100.10, PN: 30000485688x, with software version 4.2.x

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

Volcano Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Apr 13, 2022

First SIGN SARS-CoV-2 Antigen Test

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

WHPM Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

Liko Universal Twinbar 670 QRH, an accessory that can be used together with most Liko lifts, model numbers 3156087 and…

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

Baxter Healthcare Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

(a) CareFusion Snowden-Pencer Plastics, Endoplastic Endoscope 10 mm, 30 degrees 7", 17.5 cm, Catalog #88-5910; (b)…

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

Carefusion 2200 Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

FORE-SIGHT ELITE Absolute Tissue Oximeter, REF: 01-06-3000, Contents: Monitor 1 EA., Accessory Kit 1 EA.

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

Edwards Lifesciences, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 6, 2022

Elmer's Pecan Egg 1oz product wrapped in polypropylene wrapper and packaged into paper cartons packaged as singles, 6…

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

Elmer Candy Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 6, 2022

Hanger-Bar 2P 45cm

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

Human Care USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

Illumina NextSeq 550Dx, REF: 20005715, CE, IVD

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

Illumina, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

MiniMed 630G: MMT-1715, MMT-1754, MMT-1755; MiniMed 670G: MMT-1740, MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762,…

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

Medtronic MiniMed

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

Revogene, For In Vitro Diagnostic use in performing nucleic acid testing in clinical laboratories. Meridian branded…

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

Meridian Bioscience Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

RayStation 4-11B, and RayPlan 1, 2, 7-11B including some service packs: RayStation 4.0 (4.0.0.14) to RayStation 5…

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

RaySearch America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 6, 2022

Siemens Dimension Vista Magnesium Flex reagent cartridge (MG) Material # 10445158, Catalog # K3057 used in the…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 30, 2022

BIOMET Sports Medicine JUGGERLOC SLOTTED REAMER: [Item # 110010371, 6MM], [Item #110010372, 7MM], [Item # 110010373,…

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

Biomet, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 30, 2022

DigniCap Delta Scalp Cooling System, Product Number: 900-1001, Labeling: The DigniCap Scalp Cooling System User Manual…

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

Dignitana, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 30, 2022

Medical Device products purchased from Family Dollar retail stores located in Alabama, Arkansas, Louisiana,…

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

Dollar Tree Distribution, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 30, 2022

Outset Tablo Console Model Number: PN-0003000 Model Number: PN-0006000

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

Outset Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 23, 2022

Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray, 22 g x 1.5" Spinal Needle with Manometer

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

Bard Peripheral Vascular Inc.

10 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 23, 2022

BioPlex 2200 REF 12000650 SYPH T PACK Syphilis Total & RPR Reagent Pack

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

Bio-Rad Laboratories, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 23, 2022

Taiyaki Variety Pack; 21.6 oz. (600g) 30 fish waffles in a units, 27 master cased to a pallet, 40 pallets to container.…

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

Fdmr, Inc. dba Suji's Korean Cuisine

FDA (openFDA food enforcement)

Food

Reported Mar 23, 2022

Honey BBQ Snack, NO MSG Seasoning packaged in the following sizes: 1. 685-A, Net Wt 21 lbs. (9.52kg). Part #020001456.…

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

PS Seasoning & Spices, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 23, 2022

All Ice Cream and Ice Cream products within expiry; manufactured by Royal Ice Cream Company; manufactured in…

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

The Royal Ice Cream Company Inc.

FDA (openFDA food enforcement)

Food

Reported Mar 23, 2022

Port City Soups Creole Gumbo 32oz glass mason jar sold by individual unit

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

Tony's Tejas Salsa

4 more products in this recall

FDA (openFDA food 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.