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 Jan 20, 2021
VERITAS Collagen Matrix - Product Usage: intended for use in reconstruction of the pelvic floor excluding transvaginal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Jan 20, 2021
Lotus Edge Valve System, Transcatheter Aortic Valve Prosthesis Premounted on Delivery System, 23mm, sterile, REF…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Boston Scientific Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 20, 2021
Pristine gel Hand Sanitizer Gel Antibacterial Gel Moisturizing, 8.45 Fl. Oz. (250 mL) Bottle, Distributed by: Universal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gaza Proveedora de Servicios de Hospedaje y Alimentacion
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Jan 20, 2021
icumedical Cogent" Hemodynamic Monitoring System - Product Usage: intended for patients for whom the monitoring of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
FDA (openFDA device enforcement)
Reported Jan 20, 2021
All EPIQ and Affiniti Ultrasound systems. Model numbers - EPIQ 5G, EPIC 5C, EPIQ 5W, EPIQ 7G, EPIC 7C, EPIQ 7W, EPIQ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound Inc.
FDA (openFDA device enforcement)
Reported Jan 20, 2021
Medisafe Distal Duck Kit and Duck Bag, Cleaner, ultrasonic, medical instrument - Product Usage: intended to keep…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Jan 13, 2021
Backroad Country Spicy Cajun Mix 9 oz (255g) plastic bag. Packed by Troyer Manufacturing Millersburg, OH 44654.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipari Foods Operating Company, LLC.
FDA (openFDA food enforcement)
Reported Jan 13, 2021
enGen Laboratory Automation System, enGen Track System, Catalog Number ENGEN - Product Usage: intended for use in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 13, 2021
Bone fixation nail. TRIGEN INTERTAN - Product Usage: indicated for fractures of the femur including simple shaft…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Jan 6, 2021
REF 3102-E, Elongated Oxygen Mask, Adult Oxygen Elongated Mask with 8' Tubing, Rx Only, CE0482, (01)00709078003172 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Westmed, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2020
AMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter, Model Number ETRN102. Box PN TRN102, Box UDI…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Applied Medical Technology Inc.
FDA (openFDA device enforcement)
Reported Dec 30, 2020
APEX Compounding System Control Panel Module, REF: 601224, Product Code AX1000 - Product Usage: intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B Braun Medical, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2020
MicroScan Pos MIC Panel Type 34 - Product Usage: For the determination of antimicrobial agent susceptibility and/or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Dec 30, 2020
Flexor Check-Flo Introducer, RPN KCFW-4.0-35-55-RB-HFANL0-HC, Order Number G56229 Flexor Introducers and Guiding…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cook Inc.
20 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2020
CryoValve SG Pulmonary Human Heart Valve. The valve is cryopreserved in a tissue culture medium containing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CryoLife, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2020
CANYON BAKEHOUSE GLUTEN FREE BAGELS EVERYTHING NET WT. 14 OZ (396g) Canyon Bakehouse, LLC Johnstown, CO 80534 UPC 8…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flowers Foods (Corporate Offices)
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 30, 2020
Revolution CT ES - Product Usage: intended for head, whole body, cardiac and vascular X-ray Computed Tomography…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2020
Viral Transport Medium, 3ml, Ref: R99, Container type: Tube, Packaged: 20 tubes/box, IVD, CVM Transport Media is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hardy Diagnostics
FDA (openFDA device enforcement)
Reported Dec 30, 2020
42 IN (107 cm) Appx 5.0 ml, 20 Drop Admin Set, Spiros, REF: 20131-01; 31" (79 cm) Admin Set w/20 Drop Integrated Clave…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 30, 2020
CACAO MARKET MARIE BELLE NEW YORK; Dark Chocolate Pearls; Ingredients: Cocoa bean, sugar, biscuit cereals (wheat flour,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Maribel's Sweets, Inc.
FDA (openFDA food enforcement)
Reported Dec 30, 2020
Star 8 Rolling Walker/Rollator, Items: 4258/ BK(Black)/ BL(Blue)/ DB(Sky Blue)/ PL(Purple)/ RD(Red)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nova Ortho-Med Inc.
FDA (openFDA device enforcement)
Reported Dec 23, 2020
CJC-1295, 2000 MCG/ML, 5 ML vial, The Guyer Institute of Molecular Medicine, Indianapolis, IN
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Nutriceuticals, LLC
16 more products in this recall
FDA (openFDA drug enforcement)
Reported Dec 23, 2020
Carl Zeiss Meditec Ag VISULENS 550 REF 2268-038 - Product Usage: is a device for measuring the refractive power of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Meditec AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 23, 2020
K-ACT Actalyke Clotting Test Tubes that are used in the: ACTALYKE XL ACTIVATED CLOTTING TIME ANALYZER, and ACTALYKE…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Helena Laboratories, Corp.
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.