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 48,196 notices were distributed nationwide, so they reach Texas too — those are in the archive.

Medical devices

Reported Aug 3, 2016

GE Inspection Technologies, LP - Phoenix v|tome|x m240 cabinet x-ray systems. A microfocus CT system used primarily for…

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

GE Inspection Technologies, LP

FDA (openFDA device enforcement)

Medical devices

Reported Aug 3, 2016

Stryker Orthopaedics Trident Constrained Liner Inserter/Impactor Tip, 22 mm, 28 mm, and 32 mm. Non Sterile Catalog…

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

Stryker Howmedica Osteonics Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 3, 2016

AUTOCOMP6 XPS High Speed Compounder REF 58810

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

The Metrix Company

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 3, 2016

Instructions for Use (IFU) for Progesterone 3 Calibrator Set, repackaged as one set/package. The Instructions for Use…

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

Tosoh Bioscience, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

Amerigel Hydrogel Wound Dressing Advanced Formula for wound management 1 oz.

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

Amerx Health Care Corp.

FDA (openFDA device enforcement)

Food

Reported Jul 27, 2016

Mountain Thins Trail Mix flavor, packaged in a stand-up film pouch (resealable), net wt. 5.3 oz. The UPC is 0 41770…

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

Brown & Haley Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 27, 2016

Carestream Touch Prime, Catalog Number 1738830, and Carestream Touch Prime XE, Catalog Number 1738822 --- Common Name:…

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

Carestream Health Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

Dimension Vista¿ Homocysteine Flex Reagent Cartridge (HCYS), Device Listing No.: D017878 is an in vitro diagnostic test…

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

CSL Behring GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

DeVilbiss Model 7305P-D Powered Suction Unit

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

DeVilbiss Healthcare LLC

FDA (openFDA device enforcement)

Food

Reported Jul 27, 2016

Morelos Whole Dried Shrimp Net. Wt. 1 oz.; El Gordo Whole Dried Shrimp Net. Wt. 1 oz.; La Azteca Whole Dried Shrimp…

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

El Gordo Spices, LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 27, 2016

MODIFIED LINEAR STANDARD/LATERAL NECK TRIALS WITH SPRING SIDES REF S-200635 and S-200636

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

Encore Medical, LP

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

ATEC CANISTER. Suction Canister with Lid 490 cc., RX Only; Suction canister used to collect fluid during a breast…

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

Hologic, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 27, 2016

Kellogg's Special K Mini Brownies Blondie, 6 ct, 4.44 oz.

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

Kellogg Company

24 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 27, 2016

Navitas Naturals Superfood Hemp bar: Creamy Peanut, Hemp, Nut Bar. Net Wt. 1.4 oz/40 G. Gluten free. Ingredients:…

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

Navitas, LLC.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 27, 2016

Parker Trach-Vac Endotracheal Tubes. Tyvek pouches, 10 per box. Product Usage: The product is an endotracheal tube with…

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

Parker Medical

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

RayStation 3.0, RayStation 3.5, RayStation 4.0, RayStation 4.5, RayStation 4.7 and RayStation 5 --- Radiation Therapy…

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

Raysearch Laboratories Ab

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

Syngo.via, picture archiving and communications system software controlled. Intended to be used for viewing,…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 27, 2016

Tosi Cappuccino Crunch Almond SuperBites, 12 bars per pack, Net Wt. 2.6 ounces, UPC 755918046106

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

Simple Health LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 27, 2016

OT1000 Series Orthopedic Surgical Tables

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

Steris Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

AngioDynamics Soft Vu Omni Flush Angiographic Catheter Model Number: 10732203

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

Depuy Synthes Trauma- Trochanteric Fixation Nail Advanced (TFNA) Blade/Screw Guide Sleeve, Surgical Instrument Part…

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

Synthes (USA) Products LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

HX2" Temperature Management Systems; The Terumo¿ HX2" Temperature Management System provides temperature control of two…

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

Terumo Cardiovascular Systems Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

Toshiba America Medical Systems Angio WorkStation: XIDF-AWS801v6.00, v6.01, and V6.10 System: INFX-8000V Bi-Plane System

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

Toshiba American Medical Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes are placed in an over-shipper…

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

WalkMed Infusion, LLC

16 more products in this recall

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.