All recall categories

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.

Medical devices

Reported Feb 16, 2022

Novalung Sensor Box (F30000163) a component of Novalung Console (F30000162)- Indicated for long-term (> 6 hours)…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Fresenius Medical Care Holdings, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 16, 2022

Lily s Peppermint Flavor Baking Chips, 7 oz. Pouch

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Lily's Sweets LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 16, 2022

THERAKOS CELLEX Photopheresis Procedural Kit, CLXUSA

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Mallinckrodt Pharmaceuticals Ireland Ltd.

FDA (openFDA device enforcement)

Food

Reported Feb 16, 2022

Quesos La Ricura Mi Ranchito Fresh Cheese with Hot Peppers, 14. 0z.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Quesos La Ricura, Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 9, 2022

OXY-1 System, Model Number 001-0500-001. Used during cardiopulmonary bypass. OXY-1 System consists of Console, Pump…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Abiomed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 9, 2022

CRYPTOCOCCAL ANTIGEN LATERAL FLOW ASSAY, IMMY, Lateral Flow Assay for the Detection of Cryptococcal Antigen in serum…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Immuno-Mycologics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 9, 2022

KWIK-STIK, Candida parapsilosis derived from ATCC 22019, REF 0726P. Packaged 2 units per pack. IVD controls.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Microbiologics Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 9, 2022

Spiration Valve System (SVS) Valve in Cartridge -A one-way endobronchial valves indicated for adult patients with…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Olympus Corporation of the Americas

FDA (openFDA device enforcement)

Medical devices

Reported Feb 9, 2022

ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 9, 2022

Wayfare Dairy Free Butter Salted & Whipped,

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

WayFare Health Foods, LLC.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 9, 2022

X060-0270, 8mm Titanium Insert, Axle Interspinous Fusion System.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

XTANT Medical

FDA (openFDA device enforcement)

Food

Reported Feb 2, 2022

Brownie Points Schmurtle 2oz Packaged in food grade cellophane only used as gift basket filler - not sold individually

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Brownie Points LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 2, 2022

GE Vscan Extend, being sold as "Vscan Extend Console"

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)

Medical devices

Reported Feb 2, 2022

Trilogy Evo, Material Numbers DS2110X11B (USA) and KR2110X15B (Korea) The Trilogy Evo ventilator provides continuous or…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Philips Respironics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 2, 2022

GAT SPORT JETFUEL DIURETIC; FOR RELIEF OF WATER WEIGHT GAIN; Muscle Defining Formula; Stimulant Free Natural Herbal…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

World Health Products LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jan 26, 2022

SonarMed AirWave Monitor Kit (Monitor, Sensor Cable, Power Cord), Item Code AW-M0001. used with endotracheal tube (ETT)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Covidien, LP

FDA (openFDA device enforcement)

Medical devices

Reported Jan 26, 2022

greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring, non-ridged, 24 racks of 50…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 26, 2022

ARIES HSV 1&2 Assay, Part Number/REF 50-10017

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Luminex Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jan 26, 2022

VITROS Immunodiagnostic Products High Sample Diluent A Reagent Pack

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ortho-Clinical Diagnostics, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 26, 2022

ZOCALO AJI LIMO DRIED CHILI PODS- ORGANIC, Dried Aji Peppers for consumer consumption. Product is vacuum sealed in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Power Selles Imports dba Culinary Collective

FDA (openFDA food enforcement)

Medical devices

Reported Jan 26, 2022

1. Sensis, material # 10764561; UDI: 04056869010137 2. Sensis Vibe Hemo, material # 11007641; UDI: 04056869010199 3.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 19, 2022

Medtronic Custom Perfusion kits, with the following product descriptions and corresponding model numbers: 1. CUSTOM…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Perfusion Systems

FDA (openFDA device enforcement)

Food

Reported Jan 19, 2022

Boba Origin Brown-Sugar Milk Tea 100% WHEY PROTEIN ISOLATE 5.5g BCAA INGREDIENTS: Whey Protein Isolate, Black Tea,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

NutraCap Labs LLC

105 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 19, 2022

RefleXion Medical Radiotherapy System - System Label: "*** refleXion REF RXM1000 ***" Physics Guide/Treatment Delivery…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Reflexion Medical, Inc.

FDA (openFDA device enforcement)

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Other states

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.