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 10, 2018
Purus Labs MYOWHEY Premium Whey Protein, Chocolate Cookie Crunch, 75 True Servings, Net Wt. 5 lb / 2.26 kg. UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Purus Labs, Inc.
FDA (openFDA food enforcement)
Reported Oct 10, 2018
smiths medical portex First Breath Adult Nasal Cannula, REF 001283, Non-flared Tips, 213 cm (7 ft.) Tubing,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Smiths Medical ASD Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 10, 2018
TrueBeam Radiotherapy Delivery System version 2.0 and 2.5 EDGE Radiotherapy Delivery System version 2.0 and 2.5 Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Varian Medical Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 10, 2018
EVERYBURGER - Burger-Shaped Chocolate Cookies: NET WT. 2.32 oz. (66 g) There are 2 packing sizes; 10 items per case and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wismettac Asian Foods (USA) dba Nishimoto Trading Co. Ltd.
FDA (openFDA food enforcement)
Reported Oct 3, 2018
Bausch + Lomb Stellaris Elite 20 GA Vit Cutter, Model BL5626, 7500 cpm, packaged in sterile pouches, 6/shipper.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 3, 2018
ESSENTIO Pacemaker
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 3, 2018
FP0191, Confidence, Bone-Lock WITHGENISTEIN AND CHLOROPHYLL, A Dietary Supplement, 60 tablets per bottle, UPC: 8 92483…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Confidence Inc./Confidence U.S.A. Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 3, 2018
Retractor System Elastic Stays (Part 3314-lG; 3316-lG; 3550-lG) Product Usage: The Retractor System Elastic Stays (Part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Oct 3, 2018
Discovery MR750w Nuclear Magnetic Resonance Imaging System labeled as the following product name sold under: Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
FDA (openFDA device enforcement)
Reported Oct 3, 2018
Visualase Thermal Therapy System, Software: Visualase Software versions 3.1.1 - 3.2, Product #: 9735542
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Oct 3, 2018
Medtronic Clip Gun Magazines are packaged in individually sealed pouches and distributed in boxes containing 5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neurosurgery
FDA (openFDA device enforcement)
Reported Oct 3, 2018
Medtronic DxTerity(TM) TRA 5F, Diagnostic Catheter, REF U5TRAN35
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Medtronic Vascular
FDA (openFDA device enforcement)
Reported Oct 3, 2018
INTEGRIS Allura 9, System Code 722018 Vascular, cardiovascular and neurovascular imaging applications, Cardiac imaging…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Electronics North America Corporation
26 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 3, 2018
TRADER JOE'S Cinnamon Coffee Cake; NET WT. 16 OZ (1 LB) 454g; SKU# 94235; UPC: 00942355
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Pin Hsiao & Associates, LLC dba Zen Bakery
FDA (openFDA food enforcement)
Reported Oct 3, 2018
The Shockwave S4 IVL Catheters are intended for lithotripsy-enhanced balloon dilatation of lesions, including calcified…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shockwave Medical, Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2018
CedarLane Organic Salads; Couscous, Veggies & Chickpeas with Citrus Dressing. NET WT 9 oz. -Gluten Free -Vegetarian…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cedarlane Natural Foods Inc/Frankly Fresh Foods Inc.
FDA (openFDA food enforcement)
Reported Sep 26, 2018
400mL, Premium, Urine Meter, 16 FR, Silicone Temperature Sensing Foley Traywith Cath-Secure Plus, Sterile, Item Code…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 26, 2018
PR1000 Pivot Rehab Bed AC powered adjustable bed.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Med-Mizer, Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2018
Endoscopic Cleaning Brush, single use, sold in kits and labeled as the following: a. Item Number DYK1002DCB, BRUSH,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2018
PATHFAST Myoglobin II reagent cartridge Catalog Number: PF1111-K PATHFAST¿ NTproBNP is a product for in-vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Polymedco, Inc.,/Polymedco Cancer Diagnostic Products, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 26, 2018
DORO LUCENT Base Unit, REF 1101.021 Headrest System used in open and percutaneous craniotomies and spinal surgeries
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pro-Med Instruments GmbH
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 26, 2018
White Corn Tortilla Chips packaged under the following brand names and sizes: 1. Shearer's White Restaurant Style Bulk,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shearers Foods, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 26, 2018
Portex Pulsator Arterial Blood Sampling Kit with Dry Lithium Heparin for Gases and Electrolytes, REF 4080P-2, Sterile,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Sep 26, 2018
IsoFlex LAL Support Surface, Model Number 2860 Product Usage: : The IsoFlex LAL support surface assists in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
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.