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 Jul 31, 2019
DaVinci Laboratories of Vermont Omega 3-1,000 in a white bottle labeled as Dim Plex, 60 count UPC Code 026664273161
Moderate riskThis product could cause temporary or reversible health problems — stop using it.FoodScience Corporation
FDA (openFDA food enforcement)
Reported Jul 31, 2019
Breast Milk Transfer Lid for use with Oral Syringe Connectors Model: 90003S-100
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Medela Inc.
FDA (openFDA device enforcement)
Reported Jul 31, 2019
Ragu Chunky Sauce Tomato, Garlic & Onion 45oz and 66oz retail sizes sold in plastic jars
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mizkan America, Inc. - Corporate
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 31, 2019
Salmon (Cut)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Topway Enterprises, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 24, 2019
Alaris Pump, Model 8100, with bezel mechanical assemblies manufactured with FR-110 plastic resin. The following…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jul 24, 2019
Advincula Delineator with Ultem Plastic Soft Cup size 2.5 cm; Part No. AD750SC-KE25 The Advincula Delineator Uterine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 24, 2019
Lay' Lightly Salted Barbecue Flavored Potato Chips Net Wt. 7 3/4 OZ. UPC Code 2840063242
High riskUsing this product could cause serious injury, illness or death — stop using it now.Frito-Lay, Inc.
FDA (openFDA food enforcement)
Reported Jul 24, 2019
Anti-fog solution packaged in a Tyvek peel pouch and it is placed into various kits. Kit are labeled as follows:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, Inc.
FDA (openFDA device enforcement)
Reported Jul 24, 2019
Wilton Chocolate decorator icing stiff consistency 16 oz plastic tub retail unit 6 or 12 retail units per wholesale unit
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Wilton Brands
FDA (openFDA food enforcement)
Reported Jul 17, 2019
Alaris Pump Infusion Set, Model Codes 10010453, 10010454, 10012144, 10015294, 10015414, 10933805, 11171447, 11404930,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Jul 17, 2019
Radrex-i X-Ray System (DRAD-3000E) TFP-4336W (Wireless FPD) Software version: v5.00ER005 Product Usage: The RADREX-I is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
FDA (openFDA device enforcement)
Reported Jul 17, 2019
Giraffe Infant Radiant Warmer Infant radiant warmers provide infrared heat in a controlled manner to neonates who are…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 17, 2019
HAMILTON-G5, with software versions less than or equal to 2.60 The HAMILTON-G5/S1 ventilators are designed for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hamilton Medical AG
FDA (openFDA device enforcement)
Reported Jul 17, 2019
ColoCARE, Cat. No. 5650, packaged 250 envelopes/box, For In-Vitro Diagnostic Use. The firm name on the label is Helena…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Helena Laboratories, Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 17, 2019
Blue Plate Light Olive Oil Mayonnaise 30oz / 18oz, PET jars and PET squeeze bottles
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Reily Foods Co., Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 10, 2019
ZOLL Pro-padz Liquid Gel Radiolucent, Part numbers: 8900-2105-01 (12/case) and 8900-2106-01 (single)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Detek, Inc.
FDA (openFDA device enforcement)
Reported Jul 10, 2019
Centricity Universal Viewer 6.0 Is a device that displays medical images and data from various imaging sources, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 10, 2019
CLEO Patient Monitor /Tranquility VS Patient Monitor
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Infinium Medical, Inc.
FDA (openFDA device enforcement)
Reported Jul 10, 2019
Vereos PET/CT, Model No. 882446 Product Usage: Positron Emission Tomography (PET) and X-ray Computed Tomography (CT)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 10, 2019
DVR Crosslock ePAK Screw Driver, Model Number 212000002 Product Usage: These DVR Express Disposable Instruments are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 9, 2019
Fairmont Foods, Inc. Recalls Ready-To-Eat Pork and Beef Gravy Products Due to Possible Foreign Matter Contamination
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fairmont Foods, Inc.
USDA FSIS
Reported Jun 26, 2019
365 by Whole Foods Market Classic Potato Salad packaged in a clear plastic clamshell 8 Oz. and a salad bar item UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Renaissance Food Group LLC
6 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 19, 2019
Prestige II, Prestige SI, Prestige VH Prestige system is a new multi-purpose conventional and digital R/F remote…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Alinity c Cuvette Segments, List Number 04S47-01 Product Usage: The Alinity c Cuvettes are used on the Alinity c system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott GmbH & Co. KG
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.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.