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 48,100 notices were distributed nationwide, so they reach Texas too — those are in the archive.
Reported Jan 29, 2025
CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Number: 828810 Implantable device that provides…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2025
Mr. Bing brand Sriracha Chili Sauce; 9 oz and 18 oz, in clear PET bottle with green cap; UPC 850044819072 and UPC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mr Bing Foods Inc.
FDA (openFDA food enforcement)
Reported Jan 29, 2025
Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number: 88231 Software Version: N/A Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.O&m Halyard, Inc.
FDA (openFDA device enforcement)
Reported Jan 29, 2025
VDR4 Phasitron Breathing Circuit Models that contain the venturi component: -A50094 D 5PK, Phasitron Kit, VDR, Single…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Percussionaire Corporation
FDA (openFDA device enforcement)
Reported Jan 29, 2025
Merlin.net Patient Care Network (PCN) Heart Failure Web Application (Model MN6000) (Which interfaces with CardioMEMS"…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St. Jude Medical
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 29, 2025
Brand Name: IMed Products Product Name: Dressing Change Kit with ChloraPrep 3mL & HaloGUARD Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trinity Sterile, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2025
McKesson Cardiology Hemo software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.A L I Technologies Ltd.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2025
Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Model/Catalog Number: 8065977763 Product Description:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2025
Idylla INSTRUMENT, IVD, REF P0010. Intended for the detection of nucleic acid targets in various types of human…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biocartis Nv
FDA (openFDA device enforcement)
Reported Jan 22, 2025
Portrait Core Services, a set of software services that enable the communication and interaction of the Portrait Mobile…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
FDA (openFDA device enforcement)
Reported Jan 22, 2025
14019 Cucumber Select 6 CT, 01034 Cucumber Select 5# packaged in polybags Dairyland Produce, LLC
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hardies Fresh Foods
FDA (openFDA food enforcement)
Reported Jan 22, 2025
Panther Fusion GBS Assay REF PRD-04484 Kit containing Panther Fusion GBS Reagent Cartridge IVD.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2025
8MM, MONOPOLAR CURVED SCISSORS, IS4000 REF 470179
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
38 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2025
OsteoCove Putty, 1.25cc, REF 56920013 and Cove Putty, 1.25cc REF 02-9200-01.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.IsoTis OrthoBiologics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2025
Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps, CE
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Jan 22, 2025
El Gallo Jalape¿o Queso salsa
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Las Delicias Distributors, LLC
FDA (openFDA food enforcement)
Reported Jan 22, 2025
Neo-Tee T-Piece Resuscitator, for pediatric emergency respiratory support, Part: 1050805, 1050808, 1050809, 1050810,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mercury Enterprises, Inc. dba Mercury Medical
FDA (openFDA device enforcement)
Reported Jan 22, 2025
Implant Epikut S Plus CM 16-Degrees 4,5 X 18,0 mm, REF: ILM 4518N
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sin Sistema de Implante Nacional S.a
FDA (openFDA device enforcement)
Reported Jan 22, 2025
DELI FRESH VEGETABLE TRAY MED, 4 lb., packaged in a plastic container with a plastic lid, UPC 11110-99274
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 22, 2025
Stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide, REF MRUE200. Indicated for use during Total Shoulder…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tornier S.A.S.
FDA (openFDA device enforcement)
Reported Jan 15, 2025
Aerin Medical VivAer Stylus, REF CAT1785 (individual stylus), and REF CAT500 (5-pack), sterile.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aerin Medical, Inc.
FDA (openFDA device enforcement)
Reported Jan 15, 2025
AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with Y-Port. Model/Catalog Number: E6-1222
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Technology Inc.
FDA (openFDA device enforcement)
Reported Jan 15, 2025
235214 Baker's Source Traditional Cornbread Mix Complete, 5 LB Bags, 30 LB Cases Foodservice Use, Human Consumption &…
High riskUsing this product could cause serious injury, illness or death — stop using it now.C.H. Guenther & Son, Inc.
FDA (openFDA food enforcement)
Reported Jan 15, 2025
Texas Harvest Product: 01035 Cucumber Sliced 5# 5-pound trays with sealed film
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dairyland Produce, LLC
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.