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.

Food

Reported Aug 1, 2018

Sweet Serenity Caramel Sea Salt Chocolate Chip Cookies, with caramel flavored chips; NET WT; 2 oz. UPC: 0 31535 59962 2…

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

Biscomerica, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 1, 2018

CORAIL Cementless Femoral Stem HA Coated Standard Size 11, Catalog No. 3L92511

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

DePuy Orthopaedics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

Brivo XR385, model 5215463, Digital Diagnostic Radiographic System

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

Leica Microsystems products labeled as the following: Leica M320 Microscope Systems with Article Numbers 10448419,…

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

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

Invia Motion Negative Pressure Wound Therapy System. Labeled as: a. Endure Negative Pressure Wound Therapy (Model…

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

Medela Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 25, 2018

T2100 Micro flex Drive Treadmill, powered Product Usage: Powered exercise equipment consist of powered devices intended…

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

GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

FDA (openFDA device enforcement)

Medical devices

Reported Jul 25, 2018

Health Harmony Mobile application software Product Usage: Care Innovations Health Harmony Mobile is intended as a…

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

Intel-GE Care Innovations LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 25, 2018

VOLISTA StandOP Surgical Light, ARD568811961 VLT600DF AIM STP; ARD568821961 VLT600DF AIM STP QL; ARD568811911 VLT600SF…

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

Maquet SAS

FDA (openFDA device enforcement)

Medical devices

Reported Jul 25, 2018

Visualase Cooled Laser Applicator System (VCLAS) labeled as: a. Part Number 9735559, Visualase¿ Cooled Laser Applicator…

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 25, 2018

Ingenuity Digital PET/CT System, Model 882446 with the following UDI's: (01)00884838059559(21)900004…

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 25, 2018

RayStation stand-alone software treatment planning system, RayStation 4.5, RayStation 4.7, RayStation 4.9 (RayPlan 1),…

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

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Medical devices

Reported Jul 25, 2018

Dimension Vista¿ CTNI Sample Diluent, KD692, SMN# 10445205

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

Siemens Healthcare Diagnostics, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 25, 2018

Reprocessed HARMONIC Ace¿ +7, 5mm Diameter Shears with Advanced Hemostasis (HARH), Item Number HARH36 Product Usage:…

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Food

Reported Jul 25, 2018

Odwalla Superfood fruit smoothie 15.2 oz. (450mL) plastic bottle; Sold in 8 pack case Unit UPC: 000-14054-06405-5…

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

The Coca-Cola Company

FDA (openFDA food enforcement)

Medical devices

Reported Jul 18, 2018

BioMerieux mini VIDAS System in combination with Quality Control VIDAS* (QCV*) Product Usage: the Quality Control VIDAS…

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

bioMerieux, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 18, 2018

Blue Bell Ice Cream, Brand Homemade Vanilla Flavored, 3 FL OZ (88 mL), Cups, 24 per box, This Unit Not Labeled For…

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

Blue Bell Creameries, LP

FDA (openFDA food enforcement)

Medical devices

Reported Jul 18, 2018

PD-L1 IHC 22C3 pharmDx is a companion diagnostic used to determine PD-L1 levels for determination of patient treatment…

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

Dako North America Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 18, 2018

Honey Mama's Oregon Peppermint Cacao-Nectar Bar wrapped in quilon parchment paper with a sticker label. Net wt. 2.5 oz,…

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

Nectar Foods LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jul 18, 2018

Vacuum Regulator, Push-T-Set Intermittent Suction Unit (PTS-ISU) Product Usage: The vacuum regulator is intended to be…

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

Ohio Medical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jul 18, 2018

Reliance 1227 Cart and Utensil Washer/Disinfector, FW03101, FW03102, FW03S003 Product Usage: The Reliance 1227 Cart and…

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

Steris Corporation

FDA (openFDA device enforcement)

Food

Reported Jul 18, 2018

Sparkling ICE Cherry Limeade Naturally Flavored Sparking Water, packaged in a PET bottles with a plastic cap, Net Wt.…

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

Talking Rain Beverage Co. Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 11, 2018

26-Lead Transfer Set for use with APEX¿ Compounding System, Product Catalog Number 2112550

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

B. Braun Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 11, 2018

Vulcan Fast Red Chromogen Kit 2, part of an immunohistochemistry (IHC) procedure using an alkaline phosphatase (AP)…

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

Biocare Medical, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 11, 2018

ECOLAB MICROTEK Rolled Probe Cover, 2.0 cm x 20 cm (.8 in x 8 in), Ref PC0905, packaged 1 probe cover/pouch, 25…

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

Ecolab Inc.

1 more product in this recall

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.