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 20, 2018

EconoMax Neopolitan, 4 quarts and 56 ounces

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

H-E-B Grocery Company LP dba Heb

14 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 20, 2018

Prima Plus ¿4.1 x 11.5mm Implant, Catalog Number 15737K Keystone Dental implants are intended for use in partially or…

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

Keystone Dental Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 20, 2018

Snak Club Tropical Trail Mix: 16 oz. plastic pouch: Ingredients: Raisins, Peanuts, Pineapple, Papaya, Banana Chips,…

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

New Century Snacks LLC

FDA (openFDA food enforcement)

Food

Reported Jun 20, 2018

Commercial breaders and batters Product B58042 Breader XI- 50 pound bags Product B58915 Breader X1- 40 pound bags…

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

Newly Weds Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jun 20, 2018

IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865350

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

Philips Electronics North America Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 20, 2018

Brilliance 64 with DEPMED HARDENING KIT 12NC: 459800191351, Model Number 728231. Computed Tomography X-ray system

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

Philips Medical Systems (Cleveland) Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 20, 2018

cobas e 801 immunoassay analyzer, cobas 8000 Modular Series The device is a fully automated, software controlled…

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

Roche Diagnostics Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 20, 2018

Sonialvision Safire II, Model #: DAR-8000f Product Usage: This angiographic x-ray system device intended to be used for…

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

Shimadzu Medical Systems

FDA (openFDA device enforcement)

Food

Reported Jun 20, 2018

Sugarfina Sugar Cookies Distributed by Sugarfina, Inc. small candy cube, large candy cube, and 1.0oz. taster packet UPC…

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

Sugarfina, LLC

FDA (openFDA food enforcement)

Meat & poultry

Reported Jun 20, 2018

Texas Natural Meats Recalls Frozen Raw Ground Beef Products

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

Texas Natural Meats

USDA FSIS

Medical devices

Reported Jun 20, 2018

Part #: SAM XT-M, Model: Tactical Black or Military

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

The Seaberg Company Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 13, 2018

Priano Rosso Pesto Sauce, 6.7oz glass jar

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

BLM Products U. Vertriebsges

FDA (openFDA food enforcement)

Medical devices

Reported Jun 13, 2018

Bardex Lubricath 3-Way 75cc Continuous Irrigation Foley Catheter (Creevy), 22Fr. Rx (01267522)

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

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 13, 2018

Alaris Extension Sets with microbore tubing Model 20022 and 30914 Is used to administer fluid and medications from a…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 13, 2018

Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-T 5208 ECC SET, Part Number 701054588

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

Datascope Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 13, 2018

Draeger Jaundice Meter JM-103 The device is intended for use in hospitals, clinics or doctor s offices under a…

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

Draeger Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 13, 2018

NaturaLyte¿ Liquid Acid Concentrate for Bicarbonate Dialysis, 3.43 Liters, Part Number: 08-3231-1 Product Usage: This…

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

Fresenius Medical Care Renal Therapies Group, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 13, 2018

Centricity PACS-IW with Universal Viewer Product Usage: Usage: Centricity PACS-IW with Universal Viewer is a device…

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

GE Healthcare

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 13, 2018

Hobbs Bronchial Cytology Brushes, Model Number 4202; 4204; 4206 To be utilized by a trained physician and/or trained…

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

Hobbs Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 13, 2018

Xper Flex Cardio Physiomonitoring System The Xper Flex Cardio physiomonitoring system is used to facilitate invasive…

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

Invivo Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 13, 2018

12C (AdaPTinsight) Affected component: AdaPTinsight software Product Usage: 12C is used with a charged particle or…

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

Ion Beam Applications S.A.

FDA (openFDA device enforcement)

Food

Reported Jun 13, 2018

Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol, Multiple sizes: 8 oz, 16 oz, 32 oz, 64 oz, 1 gal, 2.5 gals, 5…

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

Lake Michigan Distilling Co. LLC

FDA (openFDA food enforcement)

Medical devices

Reported Jun 13, 2018

Restoris MCK Onlay Insert Extractor.

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

Mako Surgical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 13, 2018

TL-HEX TruLok Hexapod System, Double Row Footplates, TL-HEX Sterile, All Sizes: 120 MM, 140 MM, 160 MM, 180 MM, 200 MM.…

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

Orthofix Srl

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.