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 Mar 22, 2023

Plato 17 Microcatheter: Straight Tip, PL17-160-000 ; 45 degree Tip, PL17-160-045; 90 degree Tip, PL17-160-090

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

Scientia Vascular, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 22, 2023

TFN-Advanced Femoral Nail 12MM/125 DEG TI CANN TFNA 200MM STERILE. Intended for temporary fixation and stabilization of…

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

Synthes (USA) Products LLC

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 15, 2023

Brussel Sprouts 98.5% of product was packaged for retail and 110 cases were bulk Brands: 4 Earth Farms, Trader Joe s,…

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

4 Earth Farms formerly Mcl Fresh Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 15, 2023

LATITUDE NXT Remote Patient Management System, LATITUDE NXT System Server Software Model 6460.

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 15, 2023

Simplexa COVID-19 Direct, REF: MOL4150; including Reaction Mix, REF: MOL4150; with previous assay definition v2

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

DiaSorin Molecular LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 15, 2023

Given Imaging SmartBar Cereal Bar; Net Weight 2.53 oz (72 g); Ingredients: glucose syrup, soy crisps, oats, pea…

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

Given Imaging Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 15, 2023

Heartsine Samaritan PAD: SAM 350P semi-automatic defibrillator, SAM 360P fully automatic defibrillator, SAM 500P…

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

HeartSine Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 15, 2023

Sprint 200 wheeled stretcher, Item numbers 1ES200-7, 1ES210-1, and 1ES211-1.

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

Linet Spol. S.r.o.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 15, 2023

PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic…

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

Preat Corp.

FDA (openFDA device enforcement)

Food

Reported Mar 8, 2023

HEILEMANN CONFISERIE WEHNACHTSFIGUREN AUS EDELVOLLMILCH-SCHOKOLADE Solid Chocolate Holiday Treats 3.5 oz box UPC…

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

Alpenland International, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 8, 2023

Ultracell Wick with 80cc Collection Bag, 20/box

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

Beaver Visitec International, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 8, 2023

Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network cards, with IP addresses from x.x.x.224 to…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 8, 2023

DRX-Compass/DR-FIT X-ray Systems with Firmware version 2.3.2.0/2.3.2.4. For use in obtaining diagnostic quality…

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

Carestream Health, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 8, 2023

Drizzilicious Mini Rice Cake bites Net Wt. 4oz and .74oz Bags Birthday Cake UPC: 857900005402 and 857900005419 Packaged…

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

Snack Innovations Inc.

7 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 1, 2023

HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short term access (<30days) to the peripheral venous…

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

Access Vascular, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 1, 2023

Caramel Corn Boys Festival 80g units UPC:4901940039432

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

Daiso California Warehouse

14 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 1, 2023

Rao's Made for Home Slow Simmered Soup, labeled as Chicken & Gnocchi, Soup in 16-ounce glass jars, 6 jars per case.…

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

Sovos Brands Intermediate, Inc.

FDA (openFDA food enforcement)

Food

Reported Mar 1, 2023

Cayenne Pepper 1 pound jars, and 5 pound jars

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

Tampico Spice Company Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 22, 2023

HydroMID 4Fr Single Lumen - Basic Kit, Model Number 80004002

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

Access Vascular, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2023

The Covera Vascular Covered Stent is a flexible, self-expanding endoprothesis comprised of ePTFE encapsulating a…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2023

NuVasive MD Pulse III Multimodality System REF 1881500 Pulse Software version 369-BL.US and 369-BLN.US

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

NuVasive Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 15, 2023

Skinny Dipped Dark Chocolate Cocoa Almonds, 3.5 oz, packaged in flexible plastic pouches inside cardboard cases.…

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

Skinny Dipped

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 15, 2023

RipCord Syndesmosis Button, REF: STA001K

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

TriMed Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 15, 2023

Identity Shoulder System Resection Planer 35mm Resection Planer

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

Zimmer, Inc.

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.