All recall categories

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.

Meat & poultry

Reported Jul 23, 2015

Brown Packing Recalls Veal Products Due To Possible E. Coli Contamination

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Brown Packing

USDA FSIS

Medical devices

Reported Jul 22, 2015

Alere i flu, Alere i, Alere Influenza A & B; Part Number (PN) 425-024 The Alere" i Influenza A & B assay, performed on…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alere Scarborough, Inc. dba Binax, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 22, 2015

Diet Bubba Cola, 20 FL. OZ (1.25 PT) 591 mL INGREDIENTS: CARBONATED WATER, HIGH FRUCTOSE CORN SYRUP, CARAMEL COLOR,…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Dr. Pepper Snapple Group Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 22, 2015

0210-312-000-Woundcare Replacement kit with soft tip; 0210-318-000; Woundcare Replacement with fan tip; 0210-318-100-…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Instruments Div.

FDA (openFDA device enforcement)

Food

Reported Jul 22, 2015

Sysco International Whole Segments Mandarin Oranges In Light Syrup Net Wt. 6 LB 10 OZ (3.01 kg) NDC: 074865629065; 6…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Sysco Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Jul 15, 2015

Nakoma-SL Anterior Cervical Plating System's Variable Single Barrel Drill Guide Product Usage: The Nakoma-SL ACP System…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alliance Partners LLC

FDA (openFDA device enforcement)

Food

Reported Jul 8, 2015

Conventional Desiccated Coconut - Medium Shred 25 lb. bags. Exp date: 20.11.2015 Item code: 001120; UPC: 086700011201…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Falcon Trading Co., Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 8, 2015

HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac transplantation in patient who are at risk of…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

HeartWare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

Medtronic DLP Femoral Arterial Cannula, models 57414, 57417, and 57421, and DLP Femoral Cannula Replacement Kit, Models…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Perfusion Systems

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

Spine Wave Access Kit, Catalog Number 10-1530 Package contents: RLSP494-Rhythmlink Monopolar Stimulating Probe and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Spine Wave, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

Infinite F500, in vitro diagnostic. Product Usage: The Tecan Infinite F500 is a multifunctional microplate reader with…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Tecan US, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2015

Natural Knee II Revision Femoral Stem, 125mm, item 6215-12-185. packaged in configuration 803/791. Knee Prosthesis…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Zimmer, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2015

BLUE BELL COUNTRY COOKIE VANILLA ICE CREAM & CHOCOLATE CHIP COOKIE SANDWICH 5.75 FL OZ (170 mL)

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Blue Bell Creameries, LP

285 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 1, 2015

LapSac Surgical Tissue Pouch. The current intended use for the LapSac Surgical Tissue Pouch is for isolating tissue…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cook Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2015

SNOBIZ CHEESECAKE SHAVE ICE FLAVOR, 10 pouches/carton; 8 cartons/case (80 pouches total per case), 104 gram per pouch,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Crystal Fresh

FDA (openFDA food enforcement)

Food

Reported Jul 1, 2015

Epi breads, 7" French Hoagie Sliced, Net Weight 10.4 lbs., Lavoi Corporation, EPI Breads, 4710 West Ledbetter, Dallas,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Lavoi Corporation d/b/a/ Epi De France

21 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 1, 2015

VersaTREK Instrument Series 240 REF 6240, Manufactured for Remel Inc. The VersaTREK System is for cultivating and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Remel Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 1, 2015

Lifesaver Single Patient Use Manual Resuscitator Product Usage: The Hudson RCI Lifesaver Single Patient Use manual…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Teleflex Medical

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2015

Cambridge House Royal Smoked Salmon Sliced Side Products are packaged in Reduced Oxygen Package (ROP). Product is…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

The Santa Barbara Smokehouse, Inc.

8 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 1, 2015

Fortex" Pedicle Screw System Continuous Radius Rod 5.5 - 50mm, X-Spine Systems, Inc., 452 Alexandersville Road…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

X Spine Systems Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2015

Chocolate covered wafers (Bocadin) in plastic packaging sold under the Mi Costenita brand and packaged and distributed…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Yoli, Inc. dba Mi Costenita

FDA (openFDA food enforcement)

Medical devices

Reported Jun 24, 2015

Amerigel Hydrogel Gauze Dressing 2 x 2, A5002. Wound Management.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Amerx Health Care Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2015

BD Viper LT System, catalog number 442839 when used in conjunction with the BD ProbeTec Chlamydia trachomatis (CT) Qx…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2015

HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and 1103 / OUS: 1100,1101,1102,1104,1104JP and 1205.…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

HeartWare Inc.

FDA (openFDA device enforcement)

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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.