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 Apr 8, 2015
Bard 100% Latex-Free Urinary Drainage Bag with Anti-Reflux Chamber and Bard EX-Lok Sampling; Product Code 154006: Lot #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Austin Grand Prize Green Salsa; 1st Runner-up Texas Hot Sauce Challenge 1992; Mfg. Exclusively for: Skins N More Inc.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Creative Foodworks, Inc.
51 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 8, 2015
Single serving pie, 7 oz., is packed in a black paper cup with clear plastic lid, with white Sour Cream Lemon sleeve…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresh Foods Of America, LLC
FDA (openFDA food enforcement)
Reported Apr 8, 2015
Medtronic Dual Chamber Temporary External Pacemaker, Model 5392. Product Usage: The temporary pacemaker is used with a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc. Cardiac Rhythm Disease Management
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Vitagel; indicated in surgical procedures (other than in neurosurgical and ophthalmic) as an adjunct to hemostasis when…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthovita, Inc., dba Stryker Orthobiologics.
FDA (openFDA device enforcement)
Reported Apr 8, 2015
Computed Tomography X-ray Systems (Brilliance CT 64-channel w/Essence technology, Brilliance iCT, Brilliance iCT SP,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2015
Ameda One-Hand Manual Breast Pump (SKU 17161) - Primary packaging is 6 pouches with Tyvek header (9.5 x 13.63 x 3.75")…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ameda, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 1, 2015
Diamondback 360 Coronary Orbital Atherectomy System, Model Number: DBEC-125. The system is indicated to facilitate…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cardiovascular Systems, Inc.
FDA (openFDA device enforcement)
Reported Apr 1, 2015
Whole Foods Market "Chocolate Cake for Two" UPC code: 246357004999 Net Wt. 11 oz (0.69lb) in a clear plastic "clam…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Food Market
FDA (openFDA food enforcement)
Reported Mar 25, 2015
Symbia E is a multi-purpose SPECT system used to detect or image the distribution of radionuclides in the body or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 25, 2015
TactiSys Quartz Pack, PN-004 400. For percutaneous catheter radiofrequency (RF) ablation of atrial cardiac arrhythmias…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St Jude Medical
FDA (openFDA device enforcement)
Reported Mar 18, 2015
GE Healthcare Proteus XR/a with wall stand model number 2260354. Intended for use in generating radiographic images of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
FDA (openFDA device enforcement)
Reported Mar 18, 2015
GROUND CUMIN STERILE TREATED PROD. OF TURKEY, 50 LBS.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Wm. E. Martin & Sons Co., Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 18, 2015
Persona Trabecular Metal Tibial Plate / Persona TM Tibia-Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2015
SMARTSET GHV Gentamicin Bone Cement. A self-curing, radiopaque, polymethyl methacrylate based cement containing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2015
Monaco radiation therapy treatment planning system. The Monaco system is used to make treatment plans for patients with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 11, 2015
KimVent Closed Suction System for Adults, Double Swivel Elbow, 12 Fr., Sterile, Distributed by Kimberly Clark Global…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Halyard Health
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 11, 2015
FERROUS SULFATE ELIXIR 220 mg/5 mL, UPC 350838778059, NDC 50383-778-05 --- HI-TECH PHARMACAL CO, INC. AMITYVILLE, NY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hi-Tech Pharmacal Co., Inc.
FDA (openFDA food enforcement)
Reported Mar 11, 2015
DynaLOC Breast Interventional Planning Software Versions 3.1 and 3.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.iCAD, Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2015
Ikaria, INOmax DSIR (Delivery System), Model 10007. Nitric oxide delivery system for use with ventilators.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.INO Therapeutics (dba Ikaria)
FDA (openFDA device enforcement)
Reported Mar 4, 2015
Adams Pantry Basics Chili Powder Net Wt. 2.82 oz (80 g) UPC: 041313017224; Adams Pantry Basics Value Size Chili Powder…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Adams Extract & Spice LLC
44 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 4, 2015
Set Screw 5.5 mm Rod - Model #7703-1600. Product Usage: The titanium alloy set screw is used to seat a 5.5 mm titanium…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet Spine, LLC
FDA (openFDA device enforcement)
Reported Mar 4, 2015
The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
FDA (openFDA device enforcement)
Reported Mar 4, 2015
Gulf Coast Brand Cumin, NET WEIGHT 3.5 lbs (1.59 kg), GULF COAST BLENDERS, INC., NEW ORLEANS, LA
High riskUsing this product could cause serious injury, illness or death — stop using it now.Gulf Coast Blenders, Inc.
5 more products in this recall
FDA (openFDA food 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.