State
73,363 recalls have nationwide distribution and so reach Texas. 12,434 additional recalls listed Texas specifically in their distribution scope.
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 2,425 (20%) are Severe.
Which agencies issued them
These figures cover only the 12,434 recalls whose distribution notice names Texas specifically. The 73,363 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
DG Health Sugar Free Daily Fiber is recalled for missing a required phenylalanine warning label. People with phenylketonuria (PKU) require this warning to safely use the product.
BMW is recalling certain 2019–2021 3-series and X3/X4 models because the seat frame may not have been welded properly to the seat rails, risking occupant injury in a crash.
Kinjo Seika Potato Yokan confection is being recalled because coconut, a major allergen, was not declared on the label. Consumers with coconut allergies should not consume this product.
Vapotherm has recalled 5,869 Low Flow Disposable Patient Circuits for the Precision Flow System due to reports of excessive condensation that may lead to rainout.
Noven Pharmaceuticals recalls Daytrana (methylphenidate) 30 mg transdermal patches nationwide due to defective delivery system components that fail shear specifications. Patients should contact their healthcare provider regarding medication alternatives.
Russell Stover Sugar Free Peanut Butter Cups are being recalled for undeclared tree nuts (pecans) on the outer packaging. The mislabeling poses a risk to consumers with tree nut allergies.
Onishi Foods Alpha Rice Mushroom Rice is recalled due to undeclared coconut allergen on the label. Consumers with coconut allergies should not consume this product.
Noven Pharmaceuticals is recalling specific lots of Daytrana (methylphenidate) transdermal patches due to a defective delivery system that is out of specification for shear. Affected lots are Lot 91956 (6/2023) and Lot 92475 (7/2023), distributed nationwide.
DePuy Orthopaedics is recalling 7 units of the Attune Revision Tibial Insert that received excess gamma radiation during manufacturing, which may degrade implant material properties.
Boehringer Ingelheim Pharmaceuticals is recalling Jardiance (Empagliflozin) 25 mg tablets due to a label mix-up affecting 69,375 bottles distributed nationwide.
CareFusion recalls 7,914 units of BD Pyxis automated medication dispensing systems after firmware was inadvertently downgraded during installation, potentially causing drawer failures and medication delivery delays.
MEITO Alphabet Chocolate 50g packages sold in multiple U.S. states and Canada were distributed with undeclared coconut allergen. Consumers with coconut allergies should not consume this product.
BA Sports Nutrition is recalling BODYARMOR SportWater due to potential plastic pieces in the product. The recall affects approximately 21 million bottles distributed across 11 states.
Volkswagen is recalling certain 2022 Taos vehicles because the fuel delivery pump may break and cause a sudden engine stall, increasing the risk of a crash.
DePuy Orthopaedics recalls 7 units of Attune Revision LPS Tibial Inserts (Part 151760118, Lot JP6452) distributed worldwide due to excessive gamma radiation during manufacturing. This overage may result in material property changes.
Onishi Foods Alpha Rice Matsutake Mushroom Rice is being recalled because the label does not declare coconut, a major allergen. The recall affects 733 units distributed in multiple US states and Canada.
DePuy Orthopaedics is recalling 7 units of the Attune Revision Limb Preservation System Tibial Insert (Lot JP9022) that received higher than specified gamma radiation doses. The over-irradiation may cause changes to implant material properties.
Igarashiseimen Kitakata Spicy Umakara Ramen is being recalled because coconut allergen is not declared on the label. Consumers with coconut allergies should not consume this product.
DePuy Orthopaedics is recalling Attune Revision LPS Tibial Insert devices (Lot JP9016) because they received excessive gamma radiation during manufacturing, which may compromise material properties.
Noven Pharmaceuticals is recalling Daytrana methylphenidate transdermal patches for a defective delivery system that fails to meet shear specifications. The recall affects specific lots distributed nationwide.
Withings Scan Monitor/ScanWatch (model hwa09) has a software defect preventing physicians from reviewing ECG recordings, which is critical to the device's FDA clearance requirement for physician-supervised use. Users should discontinue use until the defect is corrected.
Biomet recalled 12 units of its G7 Acetabular System 40mm Size D Liner because the actual implant is a 38mm Size C. The mismatch between outer labeling and the actual implant could result in wrong-size component placement during surgery.
Daiso California Warehouse is recalling Meito Milk Cocoa (12gX5P, UPC 4902757444709) because coconut allergen is not declared on the label. Consumers with coconut allergies should discontinue use and return the product.
DePuy Orthopaedics is recalling Attune Posterior tibial insert implants that received excessive gamma radiation during manufacturing, which may degrade the material properties of the knee replacement component.
DeRoyal SafeLiner Suction Canister model PHESL-1000B is being recalled due to lid shrinkage that prevents proper vacuum seal formation and maintenance. The recall affects 27,200 devices distributed across multiple US states.