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 Oct 9, 2013
Selenia Full Field Digital Mammography System with software versions 5.0.x and 5.1.x The Selenia Full Field Digital…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Oct 9, 2013
Lactate Membrane units for E7077 Electrode Radiometer Medical ApS. The intended use is in vitro testing of samples of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Oct 2, 2013
Invacare Power Wheelchair, one per box To provide mobility to a person restricted to a sitting position.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Oct 2, 2013
DRI Cocaine Metabolite Assay, labeled as Multigent Cocaine Assay for Abbott Laboratories. 100 ml, IVD Mfg by:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microgenics Corp.
FDA (openFDA device enforcement)
Reported Oct 2, 2013
Reliance Endoscope Processing System (REPS), STERIS Corporation, 5960 Heisley Road, Mentor, OH 44060-1834 USA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Oct 2, 2013
Stryker Vision Mounting Arm, for use with other Stryker Endoscopy medical device products for human patients. Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Endoscopy
FDA (openFDA device enforcement)
Reported Sep 25, 2013
3M Scotchcast, Wet or Dry Cast Padding, Catalog Numbers WDP2, WDP3, WDP4, and WDP6. Intended for use in constructing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Company - Health Care Business
FDA (openFDA device enforcement)
Reported Sep 25, 2013
DiaScreen Liquid Urine Controls: Positive and Negative Assayed Liquid Quality Controls for use with Dipsticks in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Assuramed
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2013
Outlook ES pump is intended for use with B. Braun Medical Inc. Horizon Pump IV Sets. Used to regulate the flow of…
High riskUsing this product could cause serious injury, illness or death — stop using it now.B Braun Medical, Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2013
Osseotite 2 Certain Prevail 5mm(D)X 4.1mm (P) X X 11.5mm (L) Dental Implant Product Usage: Surgical placement in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet 3i, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2013
Blanketrol III, Model Number 233, Cincinnati Sub-Zero Products, Inc., 12011 Mosteller Road, Cincinnati, OH 45241…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cincinnati Sub-Zero Products Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2013
GE Healthcare, CARESCAPE Monitor B850. Intended for use in multiple areas within a professional healthcare facility.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2013
Pills bury Cinnamon Rolls with Icing, CINNA BON, USPC 1800000501, 1800052230, 12.4 oz and 2-pack USPC 1800045675,2-…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.General Mills, Inc.
FDA (openFDA food enforcement)
Reported Sep 25, 2013
ACL TOP (Base); PN 0000280000 Bench top, fully automated, random access analyzer designed specifically for in vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Laboratory Co.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2013
Responder 5 is a nurse call communication system that connects patients with staff in a hospital. The nurse call system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rauland-Borg Corp.
FDA (openFDA device enforcement)
Reported Sep 25, 2013
Sonogage EyeScan, A-Scan Biometer, Product Usage: A-Scan Biometer diagnostic device for measurement of axial eye length.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sonogage Inc.
FDA (openFDA device enforcement)
Reported Sep 18, 2013
OPERON D850 Surgical Table Product Usage: Surgical Table
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Berchtold Corp.
FDA (openFDA device enforcement)
Reported Sep 18, 2013
*** 1) Cat. 4341B; Qty. 10; Thoracentesis Tray; With Catheter; Sterile; CareFusion; 1500 Waukegan Road; McGaw Park, IL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion 2200 Inc.
FDA (openFDA device enforcement)
Reported Sep 18, 2013
ADVIA Centaur Folate (100 Tests), SMN 10310308, Cat No. 06367974 In vitro diagnostic use in the quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2013
Boston Scientific, Small Peripheral Cutting BalloonTM, Sterilized using irradiation: The Peripheral Cutting Balloon…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 11, 2013
CONFIDENCE SPINAL CEMENT SYSTEM 5CC KIT, Product Code: 2839-05-000 The CONFIDENCE Spinal Cement System is intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Spine, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 4, 2013
Avastin, (0.05 ml, 1.25 mg/0.05ml), single unit dose syringes, Clinical Specialties Compounding Pharmacy, Augusta, GA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Clinical Specialties Compounding Pharmacy
FDA (openFDA drug enforcement)
Reported Sep 4, 2013
DeRoyal Insufflation Tubing sets: 1) REF 28-0206 Insufflation Tubing, Laparoscopic Rx Only 2) REF 28-0214 Hi-Flow…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
FDA (openFDA device enforcement)
Reported Sep 4, 2013
Medtronic Custom Perfusion System. Model Numbers: 1D80R8, 1E34R1, 1F75R1, 1G49R2, 1G75R1, 1P07R8, 1P91R4, 5B15R11, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc. Cardiac Rhythm Disease Management
2 more products in this recall
FDA (openFDA device 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.