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 Jun 13, 2018

Rival Reduce Kit Locking and Non-Locking Screw D 2.0MM, D 2.7MM, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label, Part…

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

Orthofix, Inc.

19 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 13, 2018

ADVIA Centaur BNP (B-type Natriuretic Peptide), Catalog Numbers: 02816138 (100 tests), 02816634 (500 tests)

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

Siemens Healthcare Diagnostics, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Jun 12, 2018

J Bar B Foods Retira Productos De Salchicha De Res Debido A Un Ingrediente Adulterado Y Errneamente Rotulado

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

J Bar B Foods

USDA FSIS

Medical devices

Reported Jun 6, 2018

Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators, Catalog No C650-129A (00821925008700) The cord consists…

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

Gyrus Acmi, Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Jun 6, 2018

CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP), Part Number 0998-00-0800-XX & 0998-UC-0800-XX (excluding…

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

Maquet Datascope Corp. - Cardiac Assist Division

FDA (openFDA device enforcement)

Medical devices

Reported Jun 6, 2018

Medical Action Industries Inc. Blue OR Towel Non X-Ray Detectable (6 Towels per Pack) / product # AVID266 Sterile This…

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

Medical Action Industries Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 6, 2018

Heinens Organic Nut Mix Net Wt. 9 oz (255g) Distributed By Heinens, Warrensville Hts., OH 44128 UPC 0-36232-01871-1

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

Ohio Hickory Harvest Brand Products Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 6, 2018

SOMATOM go.Now, Material Number 11061618 There is a potential for a software issue that may cause the need for…

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

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 6, 2018

LINX Reflux Management System, Implant Suture, 12-17 Bead, 0.7T, Product Code LS-xx, sterile, Rx only. Labeled as: a.…

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

Torax Medical, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 6, 2018

AmerisourceBergen PF Latex SG (Surgical Glove), Sterile, Powder Free, Size 6.5, Item No. 10112

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

WRP Asia Pacific Sdn Bhd

FDA (openFDA device enforcement)

Food

Reported Jun 6, 2018

Ziyad Brand Tahini, 8oz, 16oz, ¿ gal, 32oz. , packed in glass jars

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

Ziyad Brothers Importing, Inc.

FDA (openFDA food enforcement)

Meat & poultry

Reported May 31, 2018

Eddy Packing Co., Inc. Retira Producto De Salchicha Ahumada Debido A Una Posible Contaminacin Con Materia Externa

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

Eddy Packing Co., Inc.

USDA FSIS

Medical devices

Reported May 30, 2018

Edwards Lifesciences' IntraClude Intra-Aortic Occlusion Device. Packaged in a sterile barrier system. Model Number:…

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Food

Reported May 30, 2018

Hot Dog Buns

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

Flowers Bakery Of Montgomery LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 30, 2018

ImplantDirect simply InterActive Implant, 5.0mmD X 10mmL, SBM: 3.4mmD Platform, Part #655010U, Rx, Sterile. Incorrect…

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

Implant Direct Sybron Manufacturing, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 30, 2018

Sorin Stockert Heater-Cooler System 3T, a) Item #: 16-02-81, 240 v/60 Hz; b) Item #: 16-02-82, 208 v/60 Hz; c) Item #:…

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

LivaNova USA

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 30, 2018

First Step Endoscopic Cleaning Pad, 100ml, Flexible Endoscope Bedside Pre-Clean Kit, Catalogue Number EP-3

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

Madison Polymeric Engineering

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 30, 2018

Hilltop Hearth Self-Rising Flour, Katy s Kitchen Self-Rising Flour, Springwell A1 Flour all packaged in 50 pound paper…

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

Shawnee Milling Company, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 30, 2018

Synthes Torque Limiting Handle, Part Number 03.231.013 This device is used in systems indicated for fracture fixation.

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

Synthes (USA) Products LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 23, 2018

Thoratec HeartMate 3 LVAS Implant Kit, Rx Only, Catalog # 106524US, 106524, 10652INT - LVAS KIT, HM 3 Indicated for…

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

Abbott

FDA (openFDA device enforcement)

Food

Reported May 23, 2018

DIABEATIC Chocolate Berry Crunch bar NET WT 1.4 oz (42g)Manufactured and Distributed by eBars, LLC, Franklin, TN 37064…

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

eBars

12 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 23, 2018

Nipro Blood Tubing set with Priming Set and Transducer Protectors. Each device is packaged in a film pouch with 24…

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

Nipro Medical Corporation

FDA (openFDA device enforcement)

Food

Reported May 23, 2018

Four J Charred Tomato & Basil Sauce 24 oz packaged in a glass jar, 6 units per case

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

Riba Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 23, 2018

Southmedic Sterile Disposable Scalpel Rx only Scalpels are intended to be used in various medical procedures for…

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

Southmedic, Inc.

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.