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 48,123 notices were distributed nationwide, so they reach Texas too — those are in the archive.
Reported Dec 2, 2020
Life2000 Ventilation System, including Life2000 Ventilator and Life2000 Compressor, Model MS-01-0118 - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom Manufacturing, Inc.
FDA (openFDA device enforcement)
Reported Dec 2, 2020
Box Label: ION Fully Articulating Catheter, REF 490105, VER 08 - Product Usage: used to navigate the Ion Fully…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Dec 2, 2020
Natural Grocers, Elderberries Whole Organic, 4 oz. (113g), plastic bag, UPC 0-0082-00304-3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vitamin Cottage Natural Foods Market, Inc. dba Natural Grocers
FDA (openFDA food enforcement)
Reported Nov 25, 2020
Art Of Tea - Feel Better tea; Produced and Distributed by: Art of Tea LLC, Monterey Park, CA Directions: 1 Tbsp of tea…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Art Of Tea
FDA (openFDA food enforcement)
Reported Nov 25, 2020
Alpen Clinic 100 Carbide Instruments (R100057C)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coltene Whaledent Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 25, 2020
Catalog 314-13-23, Equinoxe Cage Glenoid, Posterior Augment, Left, Medium
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 25, 2020
FC TOMATOES ROMA DICED 3/8" 1/5#; FC TOMATOES ROMA DICED 3/8" 4/5#, and FC TOMATOES ROMA DICED 3/8" 2/5# all packaged…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.FreshPoint Dallas
FDA (openFDA food enforcement)
Reported Nov 25, 2020
VNS Therapy¿ AspireSR¿ Generator
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Nov 25, 2020
COAPTITE Injectable Implant, injectable, sterile, non-pyrogenic implant composed of spherical particles (75-125 microns…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merz North America, Inc.
FDA (openFDA device enforcement)
Reported Nov 25, 2020
Elastic Traction Device, 11mm Lower. UPN: ER56041 Reference Number: ETD-D-26-235-C-N - Product Usage: indicated for use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Micro-Tech USA
FDA (openFDA device enforcement)
Reported Nov 25, 2020
Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thomas Scientific
FDA (openFDA device enforcement)
Reported Nov 21, 2020
FSIS Issues Public Health Alert for Chicken and Beef Samosa Products Containing Pastry Ingredients That Have Been…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Fsis
USDA FSIS
Reported Nov 18, 2020
SUNG HWAN E&B VIVACE Shenb Innovation of Beauty Technologyt - Product Usage: intended for use in the dermatologic and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesthetics Biomedical, Inc.
FDA (openFDA device enforcement)
Reported Nov 18, 2020
EDI Novel Coronavirus COVID-19 IgG ELISA Kit, REF: KT-1032 Per label: This kit is intended for qualitative detection of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Epitope Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 18, 2020
Strep B Carrot Broth One-Step, Ref. Z40, UDI: 00819398026499
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Hardy Diagnostics
FDA (openFDA device enforcement)
Reported Nov 18, 2020
Blood Monitoring Unit (BMU 40), model no. 701040852 - Product Usage: is to monitor blood parameters during…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular US Sales, LLC
FDA (openFDA device enforcement)
Reported Nov 18, 2020
QUIDEL Sofia SARS Antigen FIA IVD REF 20374
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quidel Corporation
FDA (openFDA device enforcement)
Reported Nov 18, 2020
Computed Tomography X-Ray System, Model uCT 530, Rx, CE, GTIN: 06971576831012 - Product Usage: ntended to produce…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shanghai United Imaging Healthcare Co., Ltd.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 18, 2020
Niobe ES System, Models 001-006000-1 and 001-006100-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stereotaxis Inc.
FDA (openFDA device enforcement)
Reported Nov 18, 2020
XTANT Medical, ## mm x ## mm x # mm x # ,Lordotic/Packaged InTice - C, Sterile R, Single Use Only, for the following…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.XTANT Medical
FDA (openFDA device enforcement)
Reported Nov 11, 2020
Model 3300 LATITUDE Programming System with installed Model 3892 ALTRUA, INSIGNIA I, NEXUS I Software Support…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Nov 11, 2020
Aestiva/5 MRI Anesthesia System - Product Usage: The Aestiva/5 MRI Anesthesia System provides the functional feature…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 11, 2020
TroClose 1200 - Product Usage: intended for use in a variety of gynecologic, general and urologic endoscopic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gordian Surgical
FDA (openFDA device enforcement)
Reported Nov 11, 2020
Chlorhexidine Gluconate 20% 0012 Medichem, S.A. NDC 53296-0012-0
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medichem S.A.
FDA (openFDA drug 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.