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.

Food

Reported Jun 5, 2019

Dole Classic Coleslaw (US) Shredded cabbage and carrots. 14 oz. US

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

Dole Fresh Vegetables

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 5, 2019

King LTS-D Kit Size 1, Model Number KLTSD431

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

King Systems Corp. dba Ambu, Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 5, 2019

Suja Organic Kombucha - Ginger Lemon: 15.2 oz. glass bottle; UPC 818617020232 DISTRIBUTED BY SUJA LIFE, LLC OCEANSIDE,…

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

Suja Life LLC

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 5, 2019

Global Pride Rattan Shoots in Brine: 24 oz. glass jar UPC: 8855273023148 Erawan Enterprise Co. Ltd Bangkok, Thailand.…

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

U.S. Tov, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 29, 2019

EV1000 Clinical Platform, Models: EV1000A, EV1000NI, EV1000CS Product Usage: EV1000A Monitor is used to optimize fluid…

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Drugs

Reported May 29, 2019

Losartan Potassium Tablets USP 25 mg 30 count bottle NDC 60429-316-30 Rx only GSMS Incorporated

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

Golden State Medical Supply Inc.

4 more products in this recall

FDA (openFDA drug enforcement)

Food

Reported May 29, 2019

Deli Cut Ham and American Sandwich 5.5 OZ.

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

Great American Marketing Company

7 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 29, 2019

DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral Sensor is a USB-driven sensor which is…

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

KaVo Dental Technologies LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2019

VITROS XT 7600 Integrated System, with V3.4 or 3.4.1 SW Product Code: 6844461 Product Usage: INTENDED USE: For in vitro…

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

Ortho-Clinical Diagnostics

FDA (openFDA device enforcement)

Medical devices

Reported May 29, 2019

Cobas¿ infinity central lab IT solution Material Number: 07154003001 Calculator/Data Processing Module, For Clinical Use

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

Roche Diagnostics Corporation

FDA (openFDA device enforcement)

Food

Reported May 29, 2019

Goji Powder (aka Wolfberry Powder)

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

Xi'an Yuensun Biological Technology Co., Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported May 29, 2019

Drill Sys 2.7, 2x105mm, stryker, Item Number 502015106

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

Zimmer GmbH

75 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2019

Abbott Alinity ci-series System Control Module software version 2.5.1; LN 3R70-01 with the following hardware: Level…

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

Abbott GmbH & Co. KG

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2019

Abbott ARCHITECT Estradiol Reagent Kit - Product Usage: The ARCHITECT Estradiol assay is a Chemiluminescent…

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

Abbott Ireland Diagnostics Division

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2019

MediPress pneumatic compression system, Half Leg-Segmental Gradient, Model #6102-S

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

Compass Health Brands (Corporate Office)

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 22, 2019

Item #13898 Raw California Orange Blossom Honey, packaged in an 18 oz jar with gold metal lid. Retail Jar UPC: 0 30042…

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

Glorybee Natural Sweeteners, Inc.

FDA (openFDA food enforcement)

Food

Reported May 22, 2019

Frozen ground tuna, 1 lb package, 20 packages/case

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

Jensen Tuna Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 22, 2019

Molift 2-Point sling bar, an accessory for Molift Mover 205. Item nos. 1430016 1430017 1430021

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

Moller Vital

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2019

Pentax Medical C2 CryoBalloon Standard Focal Catheter, Model FG 1028, Sterile, RX. Product Usage: The C2 CryoBalloon…

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

Pentax

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2019

Artis Zee (material # 10094135, 10094137, 10094141) - Product Usage: AXIOM Artis zee and Q/ Q.zen is a family of…

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

Siemens Medical Solutions USA, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 22, 2019

M200 Fall Monitoring System

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

Stanley Security Solutions Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 15, 2019

Abbott ARCHITECT cSystems ICT Module, REF 09D28-03. Product Usage: The ARCHITECT cSystems ICT (Integrated Chip…

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

Abbott Laboratories, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 15, 2019

Neuro Omega System, incorporating HaGuide software. For neurological and neurosurgical use. To monitor, record and…

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

Alpha Omega Engineering

FDA (openFDA device enforcement)

Medical devices

Reported May 15, 2019

Elekta Unity systems Product Usage: Elekta Unity using Magnetic Resonance Imaging is indicated for radiation therapy…

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

Elekta Limited

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.