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 Sep 11, 2019

Alaris EtCO2, Model 8300, UDI: 10885403830013, CareFusion for models 11634567 and 8300ADXeN933

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2019

Norm-O-Temp model 111Z

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

Cincinnati Sub-Zero Products LLC, a Gentherm Company

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2019

Titan Gel Serum Protein Control: SPE Control Cat. No 5136 1 x 2.0 mL

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

Helena Laboratories, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2019

SonarMed AirWave Monitor, Model Number M0001

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

SonarMed Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 11, 2019

Dolce Piquant Sweet and Sour 3 gallon (384 Fl OZ) and Freshmo Sweet and Sour in 3 gallon (384 Fl OZ)

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

Southern Style Mfg

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 11, 2019

Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted…

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

Stryker Communications

FDA (openFDA device enforcement)

Medical devices

Reported Sep 4, 2019

EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product Code:5905190, 14.5 Fr. Alphacurve Catheter with Standard Kit,…

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

Bard Peripheral Vascular Inc.

27 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 4, 2019

All colors and sizes of Confectionery Arts International, LLC brand Jewel Dust, a pearlescent pigment, manufactured and…

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

Confectionery Arts International, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 4, 2019

Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is fully integrated and automated instrument including…

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

Phadia Ab

FDA (openFDA device enforcement)

Food

Reported Sep 4, 2019

PreGel Lemon 50 4.4 lb (2kg) bag, Ingredients: dextrose, citric acid, mono and diglycerides of fatty acids, propane…

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

PreGel America, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 4, 2019

Roche Elecsys Anti-CCP Immunoassay Catalog # 07251670190

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

Roche Diagnostics Operations, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 4, 2019

Artis zee and Artis Q/ Q.zen Interventional Fluoroscopic X-Ray System with patient tables as follows: Systems Material…

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

Siemens Medical Solutions USA, Inc.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2019

Brand Name Burn Navigator¿ Model Numbers: Catalog 1120, Burn Navigator¿ H2 Catalog 1125, Burn Navigator¿ H2 Transport…

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

Arcos, Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Aug 28, 2019

Bakkavor Foods USA, Inc. Recalls Ready-To-Eat Chicken Salad Products Due to Misbranding and Undeclared Allergens

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

Bakkavor US - San Antonio

USDA FSIS

Medical devices

Reported Aug 28, 2019

Kit BD Max Check-Points CPO IVD EU; Catalog # 278102

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

Becton Dickinson & Co.

18 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2019

DeRoyal Enteral Safe Feeding Tubes: a) REF 54-2450R, 5 FR x 24" Polyurethane b) REF 54-2465R, 6.5 FR x 24" Polyurethane…

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

DeRoyal Industries Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 28, 2019

Archer Farms egg salad packaged in 12oz plastic cup with lid, 6 cups per case, refrigerated

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

Elevation Foods

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 28, 2019

PRO-DEX Surgical Driver Battery Pack PDBP-001 Series PRO-DEX Battery Pack, Single Pouch - PDBP-001-2 PRO-DEX Battery…

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

Pro-Dex Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2019

ABL90 FLEX Analyzer REF 393090 UDI:05700693930909

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

Radiometer America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2019

ACUSON NX2 Diagnostic Ultrasound System, Model # 11284381, RX Only, Siemens Medical Solutions, containing software…

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 Aug 28, 2019

MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914

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)

Food

Reported Aug 28, 2019

PRIVATE SELECTION FROZEN TRIPLE BERRY MEDLEY, 48 oz

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

The Kroger Co.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 21, 2019

Amy's Bowls - Broccoli & Cheddar Bake; Net Wt. 9.5 oz. (269g) Perishable - Keep Frozen. Microwave or regular oven. UPC:…

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

Amys Kitchen Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 21, 2019

K-Wire HBS Sterile, Item Number 19688 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS…

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

BioPro, Inc.

20 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.