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 Jul 3, 2019

Freedom EVO 200 - Product Usage: It is intended for routine laboratory tasks, such as general purpose pipetting and…

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

Tecan US, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 26, 2019

LEEP Precision Integrated System 120V, Model LP-10-120 Product Usage: The LEEP PRECISION INTEGRATED SYSTEM l 20V…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 26, 2019

Aquarius D13S319 Plus Deletion Probe, Model LPH068-A Product Usage: The D13S319 probe, labelled in red, covers a 156kb…

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

Cytocell Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 26, 2019

ETHIBOND EXCEL¿ Polyester Suture-ETHIBOND Green 75cm USP1 Single Armed CT-1 Product Code: X425H Product Usage: ETHIBOND…

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

Ethicon, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 26, 2019

2.7 Degree Angled Sagittal Saw attachment (Mako Total Knee Application Only)

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

Mako Surgical Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 26, 2019

Cepheid Xpert C. difficile/Epi Control Panel

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

Microbiologics Inc.

FDA (openFDA device enforcement)

Food

Reported Jun 26, 2019

Pasteurized donor human breast milk, Pool 9029, Batch 1 packaged in 3 ounce (90 cc) plastic bottles

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

Mothers' Milk Bank at Austin

FDA (openFDA food enforcement)

Food

Reported Jun 26, 2019

365 by Whole Foods Market Classic Potato Salad packaged in a clear plastic clamshell 8 Oz. and a salad bar item UPC…

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

Renaissance Food Group LLC

6 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jun 19, 2019

Cool Haus Awesome Dessert - Dairy Free Horchata Frozen Dessert Sandwich. Horchata Rice Milk & Cinnamon frozen dessert…

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

Coolhaus

FDA (openFDA food enforcement)

Medical devices

Reported Jun 19, 2019

IntraClude Intra-Aortic Occlusion Device, REF: ICF100, 10.5 Fr (3.5 mm) X 39.4" (100 cm), Rx Only, Sterile EO The…

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jun 19, 2019

xTAG Gastrointestinal Pathogen Panel intended for the simultaneous qualitative detection and identification of multiple…

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

Luminex Molecular Diagnostics

FDA (openFDA device enforcement)

Food

Reported Jun 19, 2019

CHOCOLATE MILK CHOCOLATE MEIJI, 1.75 oz. Item number 70378 UPC 074410703783 - only on those bars with English labeling.…

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

Wismettac Asian Foods, Inc.

6 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 12, 2019

Alinity c Cuvette Segments, List Number 04S47-01 Product Usage: The Alinity c Cuvettes are used on the Alinity c system…

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

Abbott GmbH & Co. KG

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

MRSASelect, IVD, REF 63747, containing 20 plates per package. The MRSASelect is indicated for use in conjunction with…

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

Bio-Rad Laboratories, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution

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

Kerr/Pentron, dba Kerr Corporation and Pentron Clinical

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

Leica Cryostats, used to produce frozen sample sections for biological, medical and industrial applications, including…

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

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI: 70845357041226 Product Usage: On April 9, 2019,…

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

Microbiologics Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

NxStage PureFlow B Solution, REF RFP-400, M535RFP4000 Product NxStage PureFlow B Solution is indicated for use with…

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

NxStage Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 12, 2019

ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV16F

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

OriGen Biomedical, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Jun 12, 2019

Pasture Raised Foods, LLC Recalls Raw Whole Poultry Products Produced Without Benefit of Inspection

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

Pasture Raised Foods, LLC

USDA FSIS

Medical devices

Reported Jun 12, 2019

Stryker Neurovascular, AXS Infinity LS Plus Long Sheath, Rx Only, Sterile EO, USA Customer Service 855-91 NEURO…

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

Stryker Neurovascular

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2019

Alinity i Processing Module, 03R65 01, with the below components. a. TED (Thermo Electric Device) Engine, Reagent…

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

Abbott GmbH & Co. KG

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2019

Abbott MitraClip XTR Clip Delivery System, UDI: 08717648226366, Part: CDS0601-XTR, Sterile EO, Rx Only

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

Abbott Vascular

FDA (openFDA device enforcement)

Medical devices

Reported Jun 5, 2019

Horizon Cardiology Hemo

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

Change Healthcare Israel Ltd.

1 more product 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.