Recalls distributed in Texas
These notices name Texas 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.
6,720 stored notices name Texas, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Texas too — those are in the archive.
Reported Oct 24, 2018
GE Healthcare MRI Systems, Software Version 11.x, sold under the following product names: 1.5T CXK4 LCC MAGNET,1.5T…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 24, 2018
La Mexicana Hot Salsa 16 oz., 24 oz., 48 oz., 64 oz., and 128 oz. Gourmet Style Hot Salsa 16 oz.
High riskUsing this product could cause serious injury, illness or death — stop using it now.La Mexicana LLC
6 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 24, 2018
Mindray BeneVision Distributed Monitoring System (DMS), Part No. 115-034413-00
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Oct 24, 2018
Reinforced Dual Lumen Cannula, 13Fr., REF: VV13F, Sterile EO; and ECMO Reinforced Dual Lumen Cannula, 13Fr., REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OriGen Biomedical, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 24, 2018
Quest Protein Bar Vanilla Almond Crunch Single Bar UPC# - 888849000494 12 ct. Box UPC # - 888849000500
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Quest Nutrition, LLC
FDA (openFDA food enforcement)
Reported Oct 24, 2018
Terumo¿ Advanced Perfusion System 1 Electronic Patient Gas System, Catalog#: 801188
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Oct 24, 2018
Thoratec CentriMag Motor, Model: 102956, a component of the Thoratec CentriMag Blood Pumping System and PediMag Blood…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec Switzerland GmbH
FDA (openFDA device enforcement)
Reported Oct 24, 2018
Valeris Medical Apollo Medial Suture Anchor, Catalog Number MSA-4515, 4.5 x 15mm, each package contains (1) PEEK Screw,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Valeris Medical, LLC
FDA (openFDA device enforcement)
Reported Oct 24, 2018
Affixus Hip Fracture Nail 125 9 mm x 180 mm, Item Number 814309180 Product Usage: Intended for the fixation of fractures
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
47 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 19, 2018
GHSW, LLC Recalls Salad Products Due To Possible Salmonella And Listeria monocytogenes Contamination In Corn
High riskUsing this product could cause serious injury, illness or death — stop using it now.F&S Fresh Foods
USDA FSIS
Reported Oct 19, 2018
SK Food Group Recalls Chicken Products due to Possible Salmonella and Listeria monocytogenes Contamination in Vegetables
High riskUsing this product could cause serious injury, illness or death — stop using it now.SK Food Group
USDA FSIS
Reported Oct 17, 2018
Enterprise Imaging Desktops Enterprise Imaging Desktops (Radiology Suite/Cardiology Suite) when deployed as a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Agfa Healthcare NV
FDA (openFDA device enforcement)
Reported Oct 17, 2018
Codan Filter (Codan catalog number BC 693) used with Medrad Patient Administration Sets (PAS) and Intego PET Infusion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bayer Medical Care, Inc.
FDA (openFDA device enforcement)
Reported Oct 17, 2018
Colpo-Pneumo Occluder, Part CPO-6
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Oct 17, 2018
NeoMed Enteral Feeding Tubes with Enteral Only Connectors, French sizes 4.0Fr, 5.0Fr, 6.5Fr, 8.0Fr, and lengths 40cm,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neomed Inc.
FDA (openFDA device enforcement)
Reported Oct 17, 2018
Miso Milo Chocolate (cookies); A Sarap Asian Fusion Product; Net Wt. 70 G/Cookie; Contains: Flour, eggs, Baking Soda,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sarap Asian Fusion
3 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 17, 2018
THYROID POWDER USP, Full Strength (Levothyroxine labeled range of 103-125mcg/grain; Liothyroine (correct spelling…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Syntec Pharma Corp.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Oct 16, 2018
Prime Deli Corporation Recalls Salads Containing Meat Products due to Possible Salmonella and Listeria monocytogenes…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Prime Deli Corporation
USDA FSIS
Reported Oct 15, 2018
A La Carte Foods Properties, LLC Recalls Meat and Poultry Products Containing Meat Produced without Benefit of…
High riskUsing this product could cause serious injury, illness or death — stop using it now.A La Carte Foods Properties, LLC
USDA FSIS
Reported Oct 10, 2018
Trader Darwin s Chewable Peppermint Flavored Melatonin Dietary Supplement Number of units per package: 100 tablets…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Church & Dwight Co.
FDA (openFDA food enforcement)
Reported Oct 10, 2018
Laparoscopy Instruments Instructions For Use (IFU) for the following: 1)Monopolar electrode, 2) Insert, handle and/or…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dannoritzer Medizintechnik GmbH & Co. KG
FDA (openFDA device enforcement)
Reported Oct 10, 2018
ENDOLOGIX AFX Endovascular AAA System, Stent Graft System, Rx Only, Sterile EO, REF: BA22-120/I20-40, BA22-100/I20-40,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Endologix
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 10, 2018
Formed Hash Brown Patties, packaged in cardboard trays covered with plastic film, frozen products. The following brands…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lamb Weston Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 10, 2018
Crazy About Cookies***GLUTEN FREE CHOCOLATE CHIP COOKIE DOUGH**Net Wt. 2 lbs. (907.18g)**Nutrition facts***Ingredients:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Neighbors LLC
FDA (openFDA food 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.