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.
Reported Nov 6, 2019
SPROTTE Lumbar with Introducer, labeled as the following: 1. Sprotte 22G x 90mm w/ introducer and wings (25/box); 2.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pajunk GmbH
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Glam Day Nougat Candy packaged in 6-ounce (170g) plastic packages containing individually wrapped units identified only…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Rong Shing Trading NY Inc.
FDA (openFDA food enforcement)
Reported Nov 6, 2019
Synchro2, 0.014 in x 200cm, SOFT Guidewire with Hydrophilic Coating, UPN Product No. M00326010 REF 2601, STERILE: EO -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
7 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 6, 2019
Posey Connected Twice-As-Tough Cuffs
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tidi Products
FDA (openFDA device enforcement)
Reported Nov 4, 2019
Padrino Foods, LLC Retira Productos De Carne De Res Debido A Un Error De Rotulación
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Padrino Foods LLC
USDA FSIS
Reported Oct 30, 2019
Emerald Diluent Tubing, List number 09H50-01, accompanying CELL-DYN Emerald instrument, List number 09H39-01. The firm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Oct 30, 2019
EXACTAMIX Empty EVA (Ethylene Vinyl Acetate) TPN Bag with the following product code and sizes: 1. H938737, 250mL; 2.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Canister HFC-134a /1000g, ALUM Product Number: 1600-00-0218 Revision .0C Coolant canister for use with surgical laser.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Candela Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Ergo 3.2mm K-wire - Product Usage: The devices is used assist the surgeon in the implantation of Equinoxe Shoulder…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Oct 30, 2019
ApexPro Telemetry Server System. Also identified as Modification To: ApexPro Telemetry System and ApexPro FH Telemetry…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Irrisept Wound Debridement and Cleansing System. 12 units per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.IrriMAX Corporation
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Semi-Rigid Suction Canister, 3000cc. Model Numbers OR530 and OR530H. For OR530, the product comes in a case with two…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Roland Brand Black Caviar - Whole Grain Lumpfish (Lumpfish Roe) packed in glass jars - 2oz & 2x2oz, UPC: 41224200029;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Roland Foods, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 30, 2019
GRIPPER Needles sold individually. Labeled as the following item descriptions: 1. NDL, GRIPPER, 22G X 1" (25MM), 12/BX;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 30, 2019
Tia Rita's Spicy Southwestern Green Chile Cornbread dry mix. Packaged in 13 oz (380 g) sealed plastic bags with paper…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Truck Farm, LLC
FDA (openFDA food enforcement)
Reported Oct 30, 2019
Source Naturals Dietary Supplement Brain Charge Advanced Cognitive Support 30 tablets, 60 tablets Manufactured for:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Threshold Enterprises Ltd.
FDA (openFDA food enforcement)
Reported Oct 29, 2019
H&T Seafood, Inc. Retira Productos Siluriformes Sin El Beneficio De La Inspeccin
High riskUsing this product could cause serious injury, illness or death — stop using it now.Recalling firm not stated
USDA FSIS
Reported Oct 23, 2019
Nana's Been a Nut Bread NET WT. 11oz/311.74g cloth bag CONTAINS WHEAT AND SOY. MADE ON EQUIPMENT THAT MAKES PRODUCTS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gullah Gourmet, Inc.
FDA (openFDA food enforcement)
Reported Oct 23, 2019
Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters labeled as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical Inc.
21 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 23, 2019
Roche Diagnostics cobas Integra Albumin Gen.2 Catalog Number: 05166861190 - Product Usage: In vitro test for the…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Roche Diagnostics Operations, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 23, 2019
Electrosurgical Tip Cleaner REF: 138029 Product Usage: electrosurgical accessory
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Xodus Medical Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 16, 2019
BioEnvelope, surgical mesh envelope. Labeled as the following: 1. BioEnvelope (Medium) (single pack); 2. BioEnvelope…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aziyo Biologics
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 16, 2019
Clinical Chemistry, ABX Pentra Lipase CP, ABX Pentra 400/Pentrac400, REF: A11A01631, Model/Part # 1220001631, UDI #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Horiba Instruments Incorporated
FDA (openFDA device enforcement)
Reported Oct 16, 2019
Online TDM Vancomycin Gen.3 (100 tests) Catalog # 06779336190 Analyzer/Module: cobas c 311 and cobas c 501/502
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
4 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.