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 May 17, 2017
Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 17, 2017
CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit and also part of the lnflatoball Pessary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported May 17, 2017
NDI P7 Position Sensor, Stereotaxic Instrument
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthosoft, Inc. dba Zimmer CAS
FDA (openFDA device enforcement)
Reported May 17, 2017
Reser's Fine Foods, American Classics Macaroni Salad, Net Wt 1 lb. (454 g) UPC 7117.19007, packaged in 16 oz plastic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Reser's Fine Foods, Inc.
FDA (openFDA food enforcement)
Reported May 17, 2017
Vertical Pharmaceuticals OB Complete with DHA Prenatal Multivitamin, 60 softgels Rx Only, Manufactured for: Vertical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vertical Pharmaceuticals, Inc.
FDA (openFDA food enforcement)
Reported May 10, 2017
The JETSTREAM is a rotational atherectomy catheter system designed for use in debulking and treating vascular disease…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported May 10, 2017
Schiller AG ISA CO2 Sensor (AKA: PhaseIn Unit), Merge Part Number HW-HEMO-00001. The PhaseIn Unit is an optional…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported May 10, 2017
Accu-Chek Connect Diabetes Management App versions 2.0.0, 2.0.1 and 2.1.0 for iOS and Android Product Usage: This is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported May 3, 2017
ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire, Part Number: 7-10026-01,Model Number: VPR-GW-FT14.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardiovascular Systems Inc.
FDA (openFDA device enforcement)
Reported May 3, 2017
Organic Marketside Spring Mix, net Wt. 5 oz. (142g) packed in rigid plastic container, UPC code 6 8113132897 5.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresh Express Incorpated
FDA (openFDA food enforcement)
Reported May 3, 2017
HeartWare HVAD System Controller The HeartWare Ventricular Assist System (VAS is indicated for use as a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartware
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 3, 2017
Donepezil HCl tablets, 10mg, packaged in 10x10 blister packs per carton (100 Unit Dose) container, Rx only,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mckesson Packaging Services
FDA (openFDA drug enforcement)
Reported May 3, 2017
Blood Agar (TSA w/ 5% Sheep Blood) Plate, For In Vitro Diagnostic Use, Remel, Lenexa, KS 66215 Product Usage: Blood…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
FDA (openFDA device enforcement)
Reported May 3, 2017
uNion Cervical Plate System Product Usage: The uNion Cervical Plate System is intended for anterior fixation of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ulrich Medical USA Inc.
FDA (openFDA device enforcement)
Reported May 3, 2017
5.5mm Diameter x 500mm CoCr Straight Rod, Model number X077-0420. The product is packaged in plastic bags with one…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Xtant Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 26, 2017
AFC Edamame Soybeans in Pods, 8 oz , refrigerated, in cardboard container. UPC 0-23012-00261-9
High riskUsing this product could cause serious injury, illness or death — stop using it now.Advanced Fresh Concepts Corp.
FDA (openFDA food enforcement)
Reported Apr 26, 2017
Asher's Chocolate Co, Milk Chocolate (11481) Pretzel Cluster; Net Wt. 5 lb.; Asher's Chocolate Co, Milk Chocolate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ashers Chocolates/Lewistown, Inc.
86 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 26, 2017
SURESTEP Tray, Bardex I.C. Complete Care Drainage Bag, 2000 ml Drainage Bag, 16 Fr., Sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Apr 26, 2017
Hemotherm CE, model 400CE, Heater-Cooling Device
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cincinnati Sub-Zero Products Inc.
FDA (openFDA device enforcement)
Reported Apr 26, 2017
Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; Material # E2750NSB Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien Medtronic
FDA (openFDA device enforcement)
Reported Apr 26, 2017
PGCL [poly (glycolide-co-caprolactone)] Absorbable Suture, Manufacturer CP Medical, Portland OR, Sterile, Product Codes…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CP Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 26, 2017
Proteus 235, Proton Therapy System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ion Beam Applications S.A.
FDA (openFDA device enforcement)
Reported Apr 26, 2017
Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teleflex Medical
FDA (openFDA device enforcement)
Reported Apr 19, 2017
VIDAS Estradiol II, Ref 30431-01, 60 tests The VIDAS Estradiol II (E2 II) assay is intended for use on the instruments…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
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.