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 48,122 notices were distributed nationwide, so they reach Louisiana too — those are in the archive.
Reported Sep 30, 2015
The Leica ASP6025 Tissue Processor. Pathology and Hematology Departments. The Leica ASP6025 Tissue Processor is an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2015
Regard Custom Surgical Pack, Item Number: 800628; Sterile, CV0805 - CABG B. Used in cardiovascular surgical procedures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Resource Optimization & Innovation LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 30, 2015
Sam Mills Gluten Free Chocolate Chip Granola Bars with Dark Chocolate 5 bars/4.4oz Box (0.88oz each bar)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sam MillsUSA LLC
FDA (openFDA food enforcement)
Reported Sep 24, 2015
Sanderson Farms Retira Productos De Pollo Por Posible Contaminacin Con Material Extrao
High riskUsing this product could cause serious injury, illness or death — stop using it now.Recalling firm not stated
USDA FSIS
Reported Sep 23, 2015
KellBran" CANDIES, INC. creamy rich caramel popcorn Net Wt. 8 oz. (226.64 Grams) ALLERGY INFO: Manufactured in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kellbran Candies and Snacks Inc.
FDA (openFDA food enforcement)
Reported Sep 23, 2015
The Leica ASP200S/ASP300S Tissue Processor. Pathology and Hematology Departments. The Leica ASP200S/ASP300S Tissue…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Sep 16, 2015
Biomet Parsippany, NJ. 4 0 MM X 14 MM Variable Screw C-Tek Maxan Anterior Cervical Plate System. Lot 375440.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet Spine, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2015
MEDIVATORS HEMOCOR HPH700, HPH-1400TS, HPH-1000TS. Enables the perfusionist to manage the patient's hematocrit and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2015
CDI 500 Blood Parameter Monitoring System. Provides continuous, on-line monitoring of the extracorporeal partial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Sep 9, 2015
FIRMap 60mm Catheter; Size: 60 mm; Length 50.4 inches French Size Diameter: 8.5F (2.84mm) Model number : USAR064060…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Abbott Electrophysiology
FDA (openFDA device enforcement)
Reported Sep 9, 2015
SMR Shoulder/Spalla Trial Humeral Head diameter .42 mm, REF 9013.22.425; SMR Shoulder/Spalla Trial Humeral Head…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Limacorporate S.p.A
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 9, 2015
Neptune 2 Waste Management System Docking Station (120V and 230V), New and Refurbished Product Usage: The Stryker…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Sep 2, 2015
ExacTrac 6.0.x Patient Positioning System, Radiation therapy. Intended to be used to place patients at an accurately…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Sep 2, 2015
THE ORIGINAL CHICKEN FRY MIX FROM THE MAKERS OF LOUISIANA BRAND HOT SAUCE, NET WT. 9 oz. (255g), BRUCE FOODS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bruce Foods Corporation
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 2, 2015
cobas b 123 Fluid Pack COOX REF 05169992001 200 Product Usage: The cobas b 123 POC system is a fully automated POC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 2, 2015
Kroger Ground Cinnamon UPC 11110 70034 NEW WT. 18.3 oz Plastic container
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 26, 2015
Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6"), 10 Fr, (30/box), Product Code 51610. Intermittent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Frozen Jamba, Fruit & Veggie Smoothies, Green Fusion, Green Apple, Mango, Pineapple, Kiwi, Banana, Broccoli and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Inventure Foods
64 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 26, 2015
Siemens Symbia S Series system, a diagnostic analog or digital detector based planar (2- dimensional) nuclear medicine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Bronchial Double Lumen Tube Set (Left), Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and 3.0/4.0 Cannulated Screw Countersink Part #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical Ltd.
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Winco XL Convalescent Recliner - with Steel Casters Long term patient recliner (Nursing, Rehabilitation, Geriatric Home…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Winco Mfg., LLC
12 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2015
GE Optional Laser Centering Device X-ray generator.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Inspection Technologies, LP
FDA (openFDA device enforcement)
Reported Aug 19, 2015
Oasis Coil Extension Cable used with Hitachi Oasis MRI System Product Usage: The Oasis MR system is an imaging device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
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.