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.
6,813 stored notices name Texas, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Texas too — those are in the archive.
Reported Oct 7, 2026Updated Oct 13, 2026
Brand Name: Quantum PureFlow Product Name: Quantum PureFlow Standard Heat Exchanger High Flow 3/8 W Model/Catalog…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectrum Medical Srl
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
Philips IntraSight Plus REF: 797423 and 797417 100-120v-220-240v,50/60hZ, 1000 VA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Volcano Corp.
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
CHARLOTTE CLAW Screw, REF: 40122716, intended for use with CLAW II Polyaxial Compression Plating System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wright Medical Technology, Inc.
FDA (openFDA device enforcement)
Reported Oct 6, 2026Updated Oct 25, 2026
FSIS Issues Public Health Alert for Ineligible Chicken Vienna-Style Sausage Products Illegally Imported From Jamaica
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Fsis
USDA FSIS
Reported Oct 2, 2026Updated Oct 25, 2026
Inexport Logistics LLC Recalls Ineligible Pork Cracklings Products Imported From The Republic of Colombia
High riskUsing this product could cause serious injury, illness or death — stop using it now.Inexport Logistics LLC
USDA FSIS
Reported Sep 30, 2026Updated Oct 6, 2026
ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The non-invasive ForeSight oximeter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 6, 2026
Presource Convenience Kits: 1) KIT, PRE OP , Catalog Number: AMN548616A; 2) KIT, NICU ADMIT NEW HAN , Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 7, 2026
Red Blood Cells, Leukocytes Reduced
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Carter BloodCare
FDA (weekly enforcement report)
Reported Sep 30, 2026Updated Oct 6, 2026
nGenuity Patient Monitor with Capnography (ETCO2) CAT 8100E1-ST-US, CAT 8100E1-US, CAT 8100EP1, CAT 8100EP1-ST, CAT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Criticare Technologies, Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 7, 2026
Cornea
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OneLegacy
FDA (weekly enforcement report)
Reported Sep 30, 2026Updated Oct 6, 2026
Philips EPIQ Elite Diagnostic Ultrasound System Model # 795234
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound, LLC
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 7, 2026
Cornea
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rocky Mountain Lions Eye Bank
FDA (weekly enforcement report)
Reported Sep 30, 2026Updated Oct 6, 2026
SeaSpine Mariner Deformity Product Name: Extended Polyaxial Head, Attached Gimbal, 12mm REF: MD1-300010-12
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Seaspine Orthopedics Corporation
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 7, 2026
Bone
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tissue Transplant Technology, Ltd.
FDA (weekly enforcement report)
Reported Sep 30, 2026Updated Oct 7, 2026
Reese's Crunchy Peanut Ice Cream Bar, 2.0 fl. oz. ice cream bars, paper cartons containing individually wrapped ice…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Unilever North America Supply Chain Company, LLC
FDA (weekly enforcement report)
Reported Sep 30, 2026Updated Oct 6, 2026
Light Brown Sugar, Packaged in he follow configurations: 1. United, Net Wt. 50 lbs., (22.68kg). Item Number 810051.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.United Sugar Producers and Refiners
FDA (openFDA food enforcement)
Reported Sep 23, 2026Updated Sep 29, 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 (openFDA device enforcement)
Reported Sep 23, 2026Updated Sep 29, 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 (openFDA device enforcement)
Reported Sep 23, 2026Updated Sep 29, 2026
Boston Scientific Corporation StoneSmart Connect Console Contents: (1) Power Cord, (1) Power Adaptor, (1)DVI Cable, (1)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Sep 23, 2026Updated Sep 29, 2026
EWO_02512 (Catalog number 320550) For Investigational Use Only Nano Pro Un-Cannulated Demo Samples Quantity 100
Moderate riskThis product could cause temporary or reversible health problems — stop using it.embecta Medical II LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 23, 2026Updated Sep 29, 2026
Reign Medical Clench Staple System (Compression), Description/REF: 9mm x 7mm/152-30907; 11mm x 10mm/152-31110; 15mm x…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.F & A Foundation
FDA (openFDA device enforcement)
Reported Sep 23, 2026Updated Sep 29, 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 (openFDA device enforcement)
Reported Sep 23, 2026Updated Sep 29, 2026
Plum administration sets
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
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)
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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.