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 48,132 notices were distributed nationwide, so they reach Texas too — those are in the archive.

Medical devices

Reported Dec 7, 2016

MSS CASSETTE GLU/LAC/UREA (BUN) as a part of the Roche OMNI S Analyzer: cobas b 221<6>Roche OMNI S6 system The Roche…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 30, 2016

COBRA Fusion 50 Ablation System, COBRA Fusion 150 Ablation System, and COBRA Fusion Magnetic Retriever System. Model…

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

AtriCure, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 30, 2016

BM Westco Mster Mix Raised Donut Mix, 50#

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

CSM Bakery Products NA

21 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 30, 2016

ACTIS Flex Reamers SZ 0/1; 2/3; 4/5; 6/7; 8/9; 10/11; 12, Product is sold non-sterile, these instruments are packed…

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

Depuy Orthopaedics Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 30, 2016

DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-DRILLING SCREW 4.0 x 18mm Item Code: 186850018 The…

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

DePuy Spine, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 30, 2016

Greatbatch Stiffer Coaxial Micro-Introducer. Model #/ Name: 10904-001 Stiffer Coaxial Micro-Introducer 4FR; 10904-002…

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

Greatbatch Medical

FDA (openFDA device enforcement)

Food

Reported Nov 30, 2016

Organic Cacao Nibs, packaged in 200g (7.05 oz) brown bags, UPC code 661594002032

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

Level Ground Trading Limited

FDA (openFDA food enforcement)

Medical devices

Reported Nov 30, 2016

Philips Healthcare System X-ray Tomography Computed :

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

Philips Electronics North America Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 30, 2016

Blue Bunny Ice Cream Hoppin' Holidoodle ice cream 46 fl. oz. UPC 070640014644 and UPC 070640014651 (high altitude).

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

Wells Enterprises, Inc.

FDA (openFDA food enforcement)

Food

Reported Nov 30, 2016

Yoma Myanmar Tea Salad Snack - Spicy, 7 oz cello bag. Product of Myanmar

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

Yoma Myanmar

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 23, 2016

Access Ostase Calibrators, Catalog No. 37305, B83876 Product Usage: The Access Ostase Calibrators are intended to…

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

Beckman Coulter Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 23, 2016

FlexLab, Accelerator a3600 and Aptio Automation are modular systems designed to automate Pre-Analytical and…

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

Inpeco S.A.

FDA (openFDA device enforcement)

Food

Reported Nov 23, 2016

Frozen Onion Rings sold and distributed under the following private label retail brands: 1) Premium Pick 5 Mix and…

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

McCain Foods USA

FDA (openFDA food enforcement)

Medical devices

Reported Nov 23, 2016

OMNIBotics Tracker Kit -Model: RM-10000 The TOTAL KNEE SURGETICS Navigation System with iBlock (Now OMNIBotics) is…

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

Omni Life Science

FDA (openFDA device enforcement)

Medical devices

Reported Nov 23, 2016

Brilliance iCT Computed Tomography X-ray system, Model 728306

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

Philips Medical Systems (Cleveland) Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 23, 2016

Version 1.2.0 of Accu-Chek Connect Diabetes Management App (iOS) released on July 11, 2016

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

Roche Diabetes Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 23, 2016

RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U

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

Stryker Instruments Div.

FDA (openFDA device enforcement)

Meat & poultry

Reported Nov 17, 2016

La Quercia Retira Productos De Cerdo Seco Por No Estar Suficientemente Deshidratados

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

La Quercia Operating LLC

USDA FSIS

Food

Reported Nov 16, 2016

Fruit 66 Mixed Berry, 8 FL OZ (240 mL) 100% Juice Non-Carbonated. Flavored 100% Juice Blend from concentrate with other…

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

1 Epic, LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 16, 2016

AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove Clip Product is used for the occlusion of the heart's…

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

AtriCure, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 16, 2016

ReShape Integrated Dual Balloon System, Gen 1, Model No. 01-0013-001, Catalog No. RSM110 product Usage: The ReShape…

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

Reshape Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 16, 2016

FindrWIRZ Guidewire System Catalog# 40-05 Cardiology: The system is intended for use in the cardiovascular system for…

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

SentreHeart Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 16, 2016

Solo Almond Paste, 6/7 LB. Cans, Net Weight: 42 LBS. (19.09 KG.)

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

Sokol and Co.

FDA (openFDA food enforcement)

Food

Reported Nov 16, 2016

Dorothy Lynch Homestyle 8 oz., 16 oz., and 32 oz. bottles (12/case) and 128 oz. bottles (4/case)

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

Tasty Toppings Inc.

FDA (openFDA food enforcement)

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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.