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 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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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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.