The Recall Desk

State

Texas product recalls

73,570 recalls have nationwide distribution and so reach Texas. 12,438 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total
12,438
Critical
1,720
Severe
2,926
Most recent
2026-10-21

Of the 12,438 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.

These figures cover only the 12,438 recalls whose distribution notice names Texas specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27626–27650 of 86008

  • HighFDA (Devices)·Z-2154-2021·2021-08-04

    Daily Toric Contact Lenses Recalled for Misaligned Axis Mark

    CooperVision is recalling SOFMED BREATHABLES 1 DAY TORIC contact lenses (Lot W0106167) due to misaligned axis marks that can cause blurred vision. Affected lenses were distributed in the US and internationally.

    Product
    SOFMED BREATHABLES 1 DAY TORIC Power-07.00 -1.75/ 170 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2135-2021·2021-08-04

    Medtronic Endurant II Stent Graft Marker Detachment During Deployment

    Medtronic recalls Endurant II stent graft systems: the radiopaque marker bond may detach during deployment. The recall affects 18 devices in U.S. and international distribution. No illnesses or injuries reported.

    Product
    Endurant II/Endurant IIs Stent Graft System: Medtronic Endurant II Stent Graft System REF ETUF3214C102EE, ETCF3636C49EE, ETBF3216C166EE, and ETUF3614C102E. Used to treat infrarenal abdominal aortic or aortoiliac aneurysms using an endovascular approach.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-2148-2021·2021-08-04

    Contact Lens Recall: Misaligned Axis Mark May Cause Blurred Vision

    CooperVision is recalling SPECSAVERS UMERE TORIC daily disposable contact lenses with UV blocker due to a manufacturing defect in which misaligned axis marks may cause blurred vision.

    Product
    SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2139-2021·2021-08-04

    GE CARESCAPE PDM monitor SpO2 display freezes during extended use

    GE Healthcare's CARESCAPE PDM-Masimo SpO2 physiological monitor displays can freeze after extended use without power down, preventing real-time oxygen saturation monitoring.

    Product
    CARESCAPE PDM-Masimo SpO2. Physiological data monitor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2143-2021·2021-08-04

    Contact Lens Recall: Misaligned Axis Mark May Cause Blurred Vision

    CooperVision is recalling CLARITI 1 DAY TORIC contact lenses with misaligned axis marks that may cause blurred vision. The defective lenses were distributed worldwide including multiple U.S. states.

    Product
    CLARITI 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2136-2021·2021-08-04

    Medtronic Endurant IIs stent graft system marker detachment recall

    Medtronic is recalling 21 Endurant IIs stent graft systems due to radiopaque marker bond detachment during device deployment. The defect could affect surgical visualization and device positioning.

    Product
    Medtronic Endurant IIs Stent Graft System Medtronic Endurant IIs Stent Graft System REF ESBF3614C103EE and ESBF3214C103E. Used to treat infrarenal abdominal aortic or aortoiliac aneurysms using an endovascular approach.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-2147-2021·2021-08-04

    CooperVision CLARITI Contact Lenses Recalled for Misaligned Axis Marks

    CooperVision is recalling CLARITI 1 DAY TORIC contact lenses (Lot U0108940) because misaligned axis marks can cause blurred vision in patients.

    Product
    CLARITI 1 DAY TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2145-2021·2021-08-04

    Contact lens recall due to misaligned axis marking

    CooperVision Inc. is recalling FRESH DAY 1 DAY TORIC contact lenses (Lot R0121629) due to misaligned axis marks that may cause blurred vision in wearers.

    Product
    FRESH DAY 1 DAY TORIC Power -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0797-2021·2021-08-04

    Amy's Tortilla Casserole Bowls Recalled for Rubber Gasket Pieces

    Amy's Kitchen is recalling Amy's Bowls Tortilla Casserole & Black Beans due to the potential presence of rubber gasket pieces from production equipment. Consumers should not eat the product and should dispose of it or return it to the store.

    Product
    Amy's Bowls, Tortilla Casserole & Black Beans; Made with organic tomatoes & Black Beans. NET WT 9.5 oz. (269g); gluten Free - Perishable - keep frozen; UPC: 0 42272 00168 2 (individual box) Case UPC: 1-00-42272-00168-9 Microwave or regular oven. In trays with plastic overlay…
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-2142-2021·2021-08-04

    ThermoScientific Oxoid Antimicrobial Susceptibility Discs Recalled for Out-of-Specification Performance

    Remel Inc. is recalling certain lots of ThermoScientific Oxoid Antimicrobial Susceptibility Discs because they were manufactured out of specification, potentially affecting laboratory test accuracy. The recall involves 327 units distributed nationwide and to Bermuda.

    Product
    ThermoScientific Oxoid Antimicrobial Susceptibility Discs Rx only Made in the United Kingdom
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2152-2021·2021-08-04

    CooperVision CLARITI 1 DAY TORIC contact lenses recalled for axis misalignment

    CooperVision is recalling CLARITI 1 DAY TORIC contact lenses (Lot W0106186) due to misaligned placement of the axis mark, which can cause blurred vision.

    Product
    CLARITI 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2153-2021·2021-08-04

    Contact Lens Axis Mark Misalignment Causes Blurred Vision

    CooperVision's FRESH DAY 1 DAY TORIC contact lenses (lot W0106186) are recalled because misaligned axis marks can cause blurred vision. Affected lenses were distributed worldwide, including in the US, France, Brazil, and other countries.

    Product
    FRESH DAY 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0869-2021·2021-08-04

    Now Real Food Organic Steel Cut Oats Mislabeled with Wrong Product

    NOW Health Group Inc. is recalling a specific lot of Organic Steel Cut Oats that may contain Organic Beet Sugar instead of the labeled product. Affected consumers should not consume the product.

    Product
    Now Real Food Organic Steel Cut Oats, 2 lb bag, code 6295, UPC 733739062956, packed 8 bags per case; case packaging is for Now Real Food Organic Beet Sugar 3lbs bags
    Category
    Food
    Distribution
    45 states
  • SevereNHTSA·21V601000·2021-08-03

    Fuel hose leak recall in 2021-2022 Kenworth and Peterbilt trucks

    PACCAR is recalling 688 commercial trucks due to a fuel hose leak between the fuel pump and remote fuel filter head that increases fire risk. Free fuel hose replacement is being offered.

    Product
    KENWORTH — KENWORTH, PETERBILT T480, T280, T380, T370
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E070000·2021-08-03

    Bendix Intellipark Electronic Control Unit Software Recall

    Bendix is recalling Intellipark Dash Electronic Control Units that may fail to activate the parking brake, causing vehicles to move unintentionally.

    Product
    PARKING BRAKE:ELECTRICAL:CONTROL MODULE:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V595000·2021-08-02

    2021 Audi E-Tron: Unsecured glove box may interfere with air bag

    Volkswagen is recalling certain 2021 Audi E-Tron vehicles because the right hinge pin for the glove box cover may not be properly secured, potentially interfering with knee air bag deployment in a crash.

    Product
    AUDI — AUDI E-TRON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V599000·2021-08-02

    Software error may deactivate rear-view display in 2021 INFINITI Q60 vehicles

    A software error may disable the rear-view camera display in 2021 INFINITI Q60 vehicles, reducing rear visibility and increasing crash risk. Nissan will update the software at no cost.

    Product
    INFINITI — INFINITI Q50, QX80, Q60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V596000·2021-08-02

    2022 Mitsubishi Outlander seat belt retractor defect affects child restraints

    Mitsubishi is recalling certain 2022 Outlander vehicles due to seat belt retractors that may deactivate early, preventing child restraint systems from securing properly. Owners should contact MMNA at 1-888-648-7820 for free replacement.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V598000·2021-08-02

    2020 BMW X4 Engine Software Defect Disables Braking Assist

    BMW is recalling multiple 2020-2021 models, including the X4, due to engine management software that may disable braking assist. Owners should contact BMW at 1-800-525-7417 for a free software update.

    Product
    BMW — BMW, TOYOTA 745LE, X4, X3, M340I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V594000·2021-07-30

    Kawasaki Recalls Ninja H2 SX Motorcycles Due to Rear Wheel Lockup Risk

    Kawasaki is recalling 2018-2021 Ninja H2 SX motorcycles because insufficient grease in the rear hub needle-bearing may cause failure, leading to rear wheel lock-up and increased crash risk.

    Product
    KAWASAKI — KAWASAKI NINJA H2 SX, ZX1002A, ZX1002D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V593000·2021-07-30

    Kawasaki Recalls 2020-2021 Motorcycles Due to Engine Oil Valve Defect

    Kawasaki is recalling certain 2020-2021 motorcycles because an engine oil pressure relief valve may fail, causing a loss of oil pressure and potential engine stall.

    Product
    KAWASAKI — KAWASAKI Z H2, ZX1002L, NINJA H2, ZX1002N
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V590000·2021-07-30

    Airstream Recalls 2022 Interstate 24X RVs Due to Inverter Wiring Fire Risk

    Airstream is recalling 2022 Interstate 24X recreational vehicles because improperly wired inverters may increase the risk of fire. Dealers will install additional wiring and circuit breakers free of charge.

    Product
    AIRSTREAM — AIRSTREAM INTERSTATE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V591000·2021-07-30

    Entegra Coach Motorhomes Recalled for Fuel Rail Sealing Defect

    Entegra Coach is recalling certain 2018-2022 Anthem, Aspire, Insignia, and Reatta XL motorhomes. A faulty sealing washer in the fuel rail assembly may leak, creating a fire risk. Contact Entegra Coach at 1-800-517-9137 for repairs.

    Product
    ENTEGRA — ENTEGRA REATTA XL, INSIGNIA, ASPIRE, ANTHEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V592000·2021-07-30

    Ford Transit vehicles recalled for defective seat belt locking system

    Ford is recalling 2021-2022 Transit and 2021 Transit Connect vehicles because the front passenger seat belt locking retractor may deactivate, preventing child restraint securement. Unsecured child restraints increase crash injury risk.

    Product
    FORD — FORD TRANSIT CONNECT, TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide