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 Sep 23, 2026
Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bard Access Systems, Inc.
1 more product in this recall
FDA (weekly enforcement report)
Reported Sep 23, 2026
BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bd Switzerland Sarl
FDA (weekly enforcement report)
Reported Sep 23, 2026
Happiest Baby, Inc SNOO Sleep Sack, X-Small Model/Catalog Number: S2101-101 S2101-108-6 S2101-133 S2102-112 S2107-101…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Happiest Baby, Inc.
1 more product in this recall
FDA (weekly enforcement report)
Reported Sep 23, 2026
Plum administration sets
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
7 more products in this recall
FDA (weekly enforcement report)
Reported Sep 23, 2026
Intercon Foaming Pear Hand Soap With Aloe, 28.7 fl. oz., Manufactured for: Intercon Chemical Company 1100 Central…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intercon Chemical Co.
5 more products in this recall
FDA (weekly enforcement report)
Reported Sep 23, 2026
Brand Name: DASH Rapid PCR Instrument Product Name: DASH Rapid PCR Instrument Model/Catalog Number: SG-0002 Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nuclein LLC
FDA (weekly enforcement report)
Reported Sep 23, 2026
Philips Patient Information Center iX REF:866389
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America
1 more product in this recall
FDA (weekly enforcement report)
Reported Sep 23, 2026
GM Helix Implant, REF: 109.984;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straumann USA LLC
FDA (weekly enforcement report)
Reported Sep 23, 2026
Diced Jalapenos. Ingredients: Jalapeno Pepper. Net Wt: 3.75 oz. Keep Refrigerated. Distributed by: Taylor Farms Inc.,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Taylor Fresh Foods Inc.
24 more products in this recall
FDA (weekly enforcement report)
Reported Sep 23, 2026
Red Blood Cells, Leukocytes Reduced
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The American National Red Cross
1 more product in this recall
FDA (weekly enforcement report)
Reported Sep 16, 2026
Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF: 899914 899916 899918 UDI codes:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard Inc.
5 more products in this recall
FDA (weekly enforcement report)
Reported Sep 16, 2026
HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartSine Technologies Ltd.
FDA (weekly enforcement report)
Reported Sep 16, 2026
Alfalfa, Net Weight 50 lbs. bag, Product of USA, International Specialty Supply 1011 Volunteer Dr. Cookeville, TN 38506
High riskUsing this product could cause serious injury, illness or death — stop using it now.International Sprout Holdings, Inc.
FDA (weekly enforcement report)
Reported Sep 16, 2026
Apheresis Platelets, PAS, Leukocytes Reduced, Pathogen Reduced
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The American National Red Cross South Carolina Region
FDA (weekly enforcement report)
Reported Sep 16, 2026
Red Blood Cells, Leukocytes Reduced
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The American National Red Cross
2 more products in this recall
FDA (weekly enforcement report)
Reported Sep 11, 2026
Centric Compounding Issues Nationwide Recall of Glutathione, Myer’s Cocktail, and Tri-Immune Boost Due to Elevated Endotoxin Levels
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Centric Compounding
FDA (recalls & safety alerts)
FoodReported Sep 11, 2026
Whole Foods Market Issues Allergy Alert on Undeclared Egg in Cabricharme Cheese
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Whole Foods Market
FDA (recalls & safety alerts)
Reported Sep 9, 2026Updated Sep 16, 2026
Apheresis Platelets, PAS, Leukocytes Reduced, Pathogen Reduced
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American National Red Cross Blood Services SW Region
FDA (weekly enforcement report)
Reported Sep 9, 2026Updated Sep 14, 2026
Halyard medical convenience kits labeled as: 1) ENT, Model/Item Number (kit) ACEN89-01; 2) ENT, Model/Item Number (kit)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AVID Medical, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 9, 2026Updated Sep 14, 2026
Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number: 456025
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B Braun Medical Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2026Updated Sep 14, 2026
Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
19 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 9, 2026Updated Sep 14, 2026
STA Staclot Protein S, Model/Catalog Number: 00746-Reagent Lot number 273074; qualitative and quantitative factor…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostica Stago, Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2026Updated Sep 14, 2026
OLA-OLA Pounded Yam (Iyan) IYANINSTANT, NET WT. 2 lbs., 4 lbs., 5 lbs., 10 lbs, packed in flexible plastic bags.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fayus Inc.
FDA (openFDA food enforcement)
Reported Sep 9, 2026Updated Sep 14, 2026
5008X HD/HDF with Twister Blood Tubing Set Part Number 03-5350-8
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Renal Therapies Group, LLC
6 more products in this recall
FDA (openFDA device 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.