State

Texas product recalls

73,366 recalls have nationwide distribution and so reach Texas. 12,434 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total: 12,434
Critical: 1,720
Severe: 2,926
Most recent: 2026-10-07

Of the 12,434 recalls naming Texas we have scored against our rubric, 1,720 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,926 (24%) are Severe.

Which agencies issued them

These figures cover only the 12,434 recalls whose distribution notice names Texas specifically. The 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19351–19375 of 85800

CriticalFDA (Food)·F-0402-2023·2023-03-01
Ready-to-Eat Soup Recalled: Rao's Contains Undeclared Egg Allergen
Rao's Made for Home Slow Simmered Soup labeled as Chicken & Gnocchi is being recalled because it actually contains vegetable minestrone with an undeclared egg allergen. The recall affects 13,751 cases distributed across multiple states.
Product
Rao's Made for Home Slow Simmered Soup, labeled as Chicken & Gnocchi, Soup in 16-ounce glass jars, 6 jars per case. Shelf stable, refrigerate after opening.
Category
Food
Distribution
12 states
CriticalFDA (Food)·F-0370-2023·2023-03-01
Harvest Sesame Recalled for Undeclared Soy and Sesame Allergens
Daiso is recalling Harvest Sesame 94g units due to undeclared soy and sesame allergens on the label. The recall affects 317,751 units distributed across Daiso retail locations in six U.S. states and Canada.
Product
Harvest Sesame 94g units UPC:4901940041312
Category
Food
Distribution
6 states
SevereFDA (Devices)·Z-1137-2023·2023-03-01
NovaStar TS Anti-Asphyxia Valve recalled for magnetic interference risk
Draeger Medical recalls NovaStar TS Anti-Asphyxia Valves due to magnets that may interfere with implanted and non-implanted medical devices and metallic implants.
Product
NovaStar TS, Anti-Asphyxia Valve, Reusable, Material Numbers MP01576 (Size S), MP01577 (Size M), and MP01578 (Size L)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0378-2023·2023-03-01
Daiso Potato Crackers with Sardines Recalled for Undeclared Milk
Daiso potato crackers with sardines (46g) are being recalled due to undeclared milk allergen. The product was distributed across six US states and parts of Canada.
Product
Potato crackers with small sardines 46g UPC: 4901053077376
Category
Food
Distribution
6 states
SevereFDA (Food)·F-0377-2023·2023-03-01
MEITO Powdered Apple Tea recalled for undeclared milk allergen
DAISO CALIFORNIA WAREHOUSE is recalling MEITO Powdered Apple Tea 4packs because the product contains milk that is not declared on the label. Consumers with milk allergies should not consume this product.
Product
MEITO Powdered Apple Tea 4packs UPC: 4902757413606
Category
Food
Distribution
6 states
SevereFDA (Food)·F-0373-2023·2023-03-01
KASHIWADO senbei crackers recalled due to undeclared peanuts
KASHIWADO Hitoritoiro Fly Beans Senbei crackers are being recalled because the product contains peanuts that are not listed on the ingredient label. Consumers with peanut allergies should avoid this product.
Product
KASHIWADO Hitoritoiro Fly Beans Senbei UPC:4904036008213
Category
Food
Distribution
6 states
SevereFDA (Food)·F-0379-2023·2023-03-01
ITOSEIKA Chocolate Chip Cookies Recalled for Undeclared Milk Allergen
DAISO CALIFORNIA WAREHOUSE is recalling ITOSEIKA Chocolate Chip Cookies due to undeclared milk allergen on the label. Products were distributed to Daiso stores in California, Washington, Nevada, Texas, New York, New Jersey, and British Columbia.
Product
ITOSEIKA Chocolate chip cookies 10pieces UPC: 4901050137172
Category
Food
Distribution
6 states
SevereFDA (Food)·F-0381-2023·2023-03-01
KANRO Pure Gummy Candy Recalled for Undeclared Soy Allergen
KANRO Pure gummy candies are being recalled due to undeclared soy allergen on the label. The recall affects 113,205 units sold at Daiso stores across multiple states and Canada.
Product
KANRO Pure gummy Petit trigonal pyramid grape 17g 3 pieces UPC: 4901351055489
Category
Food
Distribution
6 states
SevereFDA (Food)·F-0380-2023·2023-03-01
Katoseika Chocolat Orange Candy recalled for undeclared soy allergen
Daiso California Warehouse is recalling Katoseika Chocolat Orange Candy (60g) due to undeclared soy allergen. The product was distributed to Daiso stores across multiple U.S. states and Canada.
Product
Katoseika Chocolat Orange Candy 60g UPC: 4901580002315
Category
Food
Distribution
6 states
SevereFDA (Food)·F-0366-2023·2023-03-01
Caramel Corn Boys Festival recalled for undeclared almonds and peanuts
Caramel Corn Boys Festival snack packs, distributed to Daiso stores, contain undeclared almonds and peanuts. This creates serious health risks for consumers with nut allergies.
Product
Caramel Corn Boys Festival 80g units UPC:4901940039432
Category
Food
Distribution
6 states
SevereFDA (Devices)·Z-1138-2023·2023-03-01
FDA Recalls NovaStar TS Standard Elbow Reusable Components for Magnet Interference Risk
Draeger Medical is recalling 893 units of NovaStar TS Standard elbow components due to magnets that could interfere with medical devices and metallic implants.
Product
NovaStar TS, Standard elbow, Reusable, Material Numbers MP01579 (Size S), MP01580 (Size M), and MP01581 (Size L)
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0372-2023·2023-03-01
TOHATO Nagewa Seaweed Snack Recalled for Unlisted Milk and Shellfish Allergens
TOHATO Nagewa Snack Seaweed Flavor contains undisclosed milk and shellfish allergens. The product is distributed to Daiso stores in CA, WA, Nevada, TX, NY, and NJ; consumers with these allergies should not consume.
Product
TOHATO Nagewa Snack Seaweed Flavor 71g units UPC:4901940112012
Category
Food
Distribution
6 states
SevereFDA (Food)·F-0367-2023·2023-03-01
Caramel Corn The Star Festival Recalled Due to Undeclared Almonds
Caramel Corn The Star Festival 80g units are recalled because they contain almonds that are not listed on the ingredient label. About 317,751 units were distributed to Daiso stores in six U.S. states and Canada.
Product
Caramel Corn The Star Festival 80g units UPC:4901940039647
Category
Food
Distribution
6 states
SevereFDA (Food)·F-0369-2023·2023-03-01
TOHATO Bitter Caramel Corn Snack Recalled for Undisclosed Almond Allergen
TOHATO Bitter Caramel Corn 77g units are recalled because they contain almonds not listed on the ingredient label. This poses a serious risk to consumers with almond allergies.
Product
TOHATO Bitter Caramel Corn 77g units UPC:4901940111121
Category
Food
Distribution
6 states
SevereFDA (Food)·F-0368-2023·2023-03-01
TOHATO Caramel Corn Recalled for Undeclared Almonds
TOHATO Caramel Corn products sold at Daiso stores are being recalled because almonds are present but not listed on the ingredient label, posing risk to people with almond allergies.
Product
TOHATO Caramel Corn - 80g units - UPC:4901940111107 2pieces TOHATO Caramel Corn - 23g units - UPC:4901940111138 TOHATO Caramel Corn 4 continuous pack - 40g units - UPC:4901940111152 TOHATO Bitter Caramel Corn - 77g units - UPC:4901940111121
Category
Food
Distribution
6 states
HighNHTSA·23V133000·2023-03-01
Coachmen Motorhomes Recalled for Entry Door Latch Failure
Forest River is recalling 2013 Coachmen Cross Country and 2023 Coachmen Sportscoach motorhomes because the entry door latch may fail, preventing entry or exit.
Product
COACHMEN — COACHMEN SPORTSCOACH, CROSS COUNTRY
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0375-2023·2023-03-01
Tohato Caramel Corn recalled for undeclared almond allergen
Daiso California Warehouse is recalling Tohato Caramel Corn 5-packs because almond appears in the ingredient list but is missing from the allergen Contains statement. Consumers with almond allergies who rely on the allergen statement may unknowingly consume this product.
Product
Tohato 5packs of Caramel Corn 23g units UPC:4901940111145
Category
Food
Distribution
6 states
HighFDA (Food)·F-0403-2023·2023-03-01
Cayenne Pepper Recalled for Elevated Aflatoxin Contamination
Tampico Spice Company Inc is recalling Cayenne Pepper in 1-pound and 5-pound jars due to elevated aflatoxin levels. The affected lot is #2112245, distributed across eight states.
Product
Cayenne Pepper 1 pound jars, and 5 pound jars
Category
Food
Distribution
8 states
HighFDA (Drugs)·D-0348-2023·2023-03-01
Warfarin Sodium Tablets Recalled Due to Failed Impurity and Degradation Specifications
Rising Pharmaceuticals is recalling Warfarin Sodium Tablets USP 1 mg due to failed impurities and degradation specifications. Approximately 12,216 bottles may have been distributed nationwide.
Product
Warfarin Sodium Tablets, USP 1 mg, 100-count bottle, Rx Only, Distributed by: Rising Health, LLC, Saddle Brook, NJ 07663, NDC# 57237-119-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1166-2023·2023-03-01
Diagnostic Imaging System Recalled for Potential Ceiling and Wall Collision Risk
Siemens Luminos dRF diagnostic imaging system is being recalled nationwide due to potential collision with ceilings, walls, or objects caused by default room configuration parameters. Collisions could result in serious injury to patients or staff.
Product
Luminos dRF with software VD10- A diagnostic imaging system for radiographic and fluoroscopic studies Model Number: 10094200
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1167-2023·2023-03-01
Diagnostic imaging system recalled for collision risk from default settings
Siemens Luminos dRF Max diagnostic imaging systems are being recalled due to a risk of collision with ceiling, walls, or nearby objects caused by default room configuration settings. This could result in serious injury to staff or patients.
Product
Luminos dRF Max with software VE10, VF10, VF11- A diagnostic imaging system for radiographic and fluoroscopic studie Model Number:10762471
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1159-2023·2023-03-01
IV Start Kit Recalled Due to Connector Manufacturing Defect
Cardinal Health Presource Packs IV start kits with ICU MicroClave Clear Connectors are being recalled due to a manufacturing defect that may cause fluid leaks and loss of fluid path integrity.
Product
Cardinal Health Presource Packs IV START KIT-Intended for IV Access CATALOG #: 01A4553E
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1156-2023·2023-03-01
HydroMID 4Fr Peripheral Venous Catheter Kit Recalled for Incorrect Component Labeling
Access Vascular is recalling HydroMID 4Fr Single Lumen Maximal Barrier Kits due to an incorrect component listed on the inner kit label. The error could lead to confusion and improper use of the device.
Product
HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term access (<30days) to the peripheral venous access system for intravenous therapy Product Number: 80004004
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0404-2023·2023-03-01
Cajun Seasoning recalled for elevated aflatoxin levels
Tampico Spice Company is recalling Cajun Seasoning in multiple sizes due to elevated aflatoxin contamination. Affected lots were distributed across eight states.
Product
Cajun Seasoning 1 OZ, 1 LB, 1.5 LBS, 2 LBS, 5 LBS, 6 LBS units
Category
Food
Distribution
8 states
HighFDA (Drugs)·D-0339-2023·2023-03-01
Levothyroxine sodium oral solution recalled due to subpotency
IBSA Pharma Inc. has recalled TIROSINT levothyroxine sodium oral solution nationwide due to subpotency. Some doses may contain less active ingredient than labeled. Patients should contact their healthcare provider.
Product
TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide