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 Mar 13, 2019
JANSAL VALLEY DUKKAH NET WT 2.5 oz. (71 G). The product is packaged in a circular tin can with a clear lid. UPC: 7…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Friendly Fruit Market dba Sid Wainer & Son
FDA (openFDA food enforcement)
Reported Mar 13, 2019
Maquet XS Flat Screen Monitor Holder, XS32 SPE, Configuration Part Number ARD22201040A Product Usage: This product is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge US Sales LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 13, 2019
DG Baby Gripe Water herbal supplement with organic ginger and fennel extracts, 4 FL OZ (120 mL) Liquid Dietary…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kingston Pharma LLC
FDA (openFDA food enforcement)
Reported Mar 13, 2019
Cepheid Respiratory Control Panel Catalog #8199 for in vitro diagnostic use
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
FDA (openFDA device enforcement)
Reported Mar 13, 2019
C2 CryoBalloon Controller, REF: FG-1017, with Controller Software v1.18.258 The C2 CryoBalloon Ablation System is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pentax
FDA (openFDA device enforcement)
Reported Mar 13, 2019
Raindrop Near Vision Inlay, REF: RD1-1, Sterile, Rx Only, Manufacturer ReVision Optics, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Rvo 2.0, Inc.
FDA (openFDA device enforcement)
Reported Mar 13, 2019
Big Daddy s Bold Cheese Pizza, item No. 78985. 3-Pack. Contains 9-44.53 oz. Pizzas. Net Wt. 25.04 Lbs. (11.36 kg) For…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Schwan's Global Supply Chain, Inc., Specialy Foods Plant
FDA (openFDA food enforcement)
Reported Mar 13, 2019
Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers Arthroscopic shavers can be used to abrade, cut…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Mar 11, 2019
Choice Canning Company, Inc. Recalls Chicken Fried Rice Products Due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Choice Canning Company Inc.
USDA FSIS
Reported Mar 6, 2019
Alcon or Endure Ophthalmic Microscope Product Usage: Used for low magnification visualization during ophthalmic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research Laboratories Ltd.
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Phoenix AST-s Indicator, Catalog Number 246009
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Entuit Secure Gastrointestinal Suture Anchor Set, Catalog Number GIAS-SRM-2, Order Number G35569 The Entuit Secure…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Monaco Radiation Treatment Planning (RTP) System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Mar 6, 2019
The WinStation Retinal Imager, also known as Merge Eye Station. DCF-1024 & DCF-512 Digital Imaging System Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Nita Crisp Spelt Bread Cracker, 8- & 16-ounce bags, In paper bags with a plastic window and has a re-closable ability…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nita Foods Inc.
FDA (openFDA food enforcement)
Reported Mar 6, 2019
Ottogi Ramen Sari (Extra Noodle) 3.88oz x 48ea Item #21101009 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ottogi America Inc.
16 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 6, 2019
Produce Packaging, Inc. Cauliflower, Rice 6/11 oz
High riskUsing this product could cause serious injury, illness or death — stop using it now.Produce Packaging Inc.
21 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 6, 2019
Tegral Satin Gold CL Cr¿me Cake, packaged in 50 lb. bag.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Puratos Corporation
FDA (openFDA food enforcement)
Reported Mar 6, 2019
Cardiovascular Procedure Kit (CLR MP4 COIL 2 SPIKE) Catalog Number: 140222
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Vitality¿ Spinal Fixation System. Thoracolumbosacral pedicle screw system (non-sterile). Pedicle screw fixation is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet Spine Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 27, 2019
AMIA Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 27, 2019
Stingray" Guidewire, labeled as 300cm. intended to facilitate placement of balloon dilatation catheters or other…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Feb 27, 2019
TRINIAS for diagnostic imaging and interventional procedures in cardiac angiography, neurovascular angiography,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems USA Com
FDA (openFDA device enforcement)
Reported Feb 27, 2019
Pilling COOLEY SUMP-SUCTION TUBE, REF 351547
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
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.