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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.

Medical devices

Reported Jul 8, 2026

OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG1260T SAFE-T-CENTESIS TRAY 6FR X 16CM UDI-DI…

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

Bard Access Systems, Inc.

13 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Jul 8, 2026Updated Sep 16, 2026

Red Blood Cells, Leukocytes Reduced

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

Carter BloodCare

FDA (weekly enforcement report)

Medical devices

Reported Jul 8, 2026

Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 Product Codes that include the…

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

Covidien LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2026

Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Housing Components with the below product descriptions and Part Codes.…

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

Depuy (ireland)

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2026

Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HAMILTON-C1, HAMILTON-T1 and HAMILTON-MR1…

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

Hamilton Medical AG

1 more product in this recall

FDA (openFDA device enforcement)

Consumer products

Reported Jul 8, 2026Updated Sep 16, 2026

Oribe Serene Scalp Densifying Shampoo, packaged in 8.5 fl. oz. (250 mL) bottles with UPC 840035231242 and 33.8 fl. oz.…

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

KAO USA Inc.

FDA (weekly enforcement report)

Food

Reported Jul 8, 2026

MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein Vegan Nuggets, Net Wt. 10.5 oz. (298g), packaged in a…

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

Mars Snacking

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 8, 2026

Radius VSM ECG pre-connected Set, REF: 4842, 4695

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

Masimo Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2026

Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN Model/Catalog Number: ENF060182LD / 101033086…

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

Medela Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2026

Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips…

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

Teleflex LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 8, 2026

GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers (by Region) United States (includes…

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

W L Gore & Associates, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jul 1, 2026Updated Sep 16, 2026

Determine HIV 1/2 Ag/Ab Combo 25T, Model/Catalog No. 7D2648

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

Abbott Diagnostics Scarborough, Inc.

FDA (weekly enforcement report)

Medical devices

Reported Jul 1, 2026

Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe Screw; 3070-27009 2.7mm x 9mm NL…

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

Acumed LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 1, 2026

Da Vinci ASSY, PSS, SP1098, Part Number: 380601

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Jul 1, 2026Updated Sep 16, 2026

Red Blood Cells, Leukocytes Reduced

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

LifeShare Blood Center

FDA (weekly enforcement report)

Food

Reported Jul 1, 2026

Dried Herring Fish 7 oz.

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

Prime Food Processing LLC.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 1, 2026

INZONE DETACHMENT SYSTEM, REF: M00345100950

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

Stryker Neurovascular

FDA (openFDA device enforcement)

Food

Reported Jul 1, 2026

1.5oz Zapp's Bayou Blackened Ranch Kettle Chips, Plastic Bag.

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

Utz Quality Foods, LLC

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 24, 2026

directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2

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

Accriva Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

Ritmed Neurological Sponges, Description/REF: 0.5x0.5in, Non-Sterile/55992C; 0.5x1.0in, Non-Sterile/55993C; 0.5x3.0in,…

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

AMD Medicom Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

PARACENTESIS KIT, REF: AK-00376, ASK-00376-VCU

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

Arrow International, LLC

34 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 24, 2026

azuma foods TAKO WASABI Seasoned Octopus with Wasabi PERISHABLE/KEEP FROZEN PRODUCT OF JAPAN DISTRIBUTED BY: AZUMA…

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

Azuma Foods International Inc. USA

FDA (openFDA food enforcement)

Medical devices

Reported Jun 24, 2026

BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta" Stopcocks are used to administer…

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

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Medical devices

Reported Jun 24, 2026

iLet Bionic Pancreas, REF: BB1001

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

Beta Bionics, Inc.

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.