The Recall Desk

State

Texas product recalls

72,992 recalls have nationwide distribution and so reach Texas. 12,390 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total
12,390
Critical
1,705
Severe
2,407
Most recent
2026-09-16

Of the 12,390 recalls naming Texas we have scored against our rubric, 1,705 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,407 (19%) are Severe.

These figures cover only the 12,390 recalls whose distribution notice names Texas specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8776–8800 of 85382

  • ModerateFDA (Devices)·Z-0980-2025·2025-01-29

    Stryker Surgical Burs Recalled Due to Package Label Mismatch

    Stryker Corporation is recalling surgical burs that may be packaged with incorrect labels, causing a mismatch between the device model inside and the label. Approximately 491 affected devices were distributed worldwide.

    Product
    The 3.0MM Neuro Match Head Soft Touch bur (5820-107-030) is intended to be used to cut bone and bone cement during neurosurgery, including craniotomy and spinal surgery as well as ear, nose and throat (ENT)/Otology/Neurotology/ Otorhinolaryngology, orthopedic, and general surgic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0967-2025·2025-01-29

    Otological Ventilation Tube Recalled Due to Lack of Regulatory Clearance

    Adept Medical Ltd is recalling otological ventilation tubes distributed without FDA 510(k) clearance. The recall affects approximately 2,190 units in the US.

    Product
    Otological Ventilation Tube - T-Tube 12mm - Silicone; Product Code: NZ3312;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V037000·2025-01-28

    Mitsubishi Fuso Recalls 2024 Rizon Trucks for Wiring Seal Defect

    Mitsubishi Fuso is recalling 233 2024 Rizon trucks because an improperly sealed chassis harness may allow water intrusion, causing loss of drive power and increasing crash risk.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO RIZON FEC9K (E18), RIZON FEC7K (E16)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V038000·2025-01-28

    Freightliner chassis fuel filter hoses can separate causing leak and stall

    Daimler Trucks is recalling certain 2022-2025 Freightliner Custom Chassis vehicles with Cummins L9 diesel engines because remote fuel filter hoses may separate from the fitting, causing a fuel leak and engine stall.

    Product
    FCCC — FCCC XCM, XCS, XCR, XBS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V013000·2025-01-24

    Ducati Recalls 2025 Panigale V4 S for Rear Brake Hose Heat Damage

    Ducati is recalling 2025 Panigale V4 S motorcycles because excessive heat may damage the rear brake hose, causing sudden brake loss and increasing crash risk.

    Product
    DUCATI — DUCATI PANIGALE V4 S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V034000·2025-01-24

    2025 Coachmen Catalina Travel Trailer Recall for Incorrect Weight Label

    Forest River is recalling 2025 Coachmen Catalina travel trailers because the Federal Placard lists an incorrect dry weight, which could lead to unintentional overloading.

    Product
    COACHMEN — COACHMEN CATALINA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V033000·2025-01-23

    Subaru Forester alloy wheels may be improperly attached losing stability

    Subaru is recalling certain 2025 Forester vehicles with 18-inch aluminium alloy wheels because an incorrectly specified lug seat surface can leave the wheel improperly attached.

    Product
    SUBARU — SUBARU FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V031000·2025-01-23

    Honda and Acura fuel injection software error can stall the engine

    Honda is recalling certain 2022-2025 Acura MDX Type-S, 2023-2025 Pilot and 2021-2025 Acura TLX Type-S vehicles because a fuel injection control unit software error may cause an engine stall or loss of power.

    Product
    ACURA — ACURA, HONDA MDX TYPE S, TLX TYPE S, PILOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V030000·2025-01-23

    Mack Trucks Recalls MRU and Terrapro Towing Vehicles for Missing ABS

    Mack is recalling 2010-2025 MRU and Terrapro towing vehicles because they lack the anti-lock brake warning light and circuitry for attached trailers.

    Product
    MACK — MACK MRU, TERRAPRO (TE)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25102·2025-01-23

    Children's Holiday Pajama Sets recalled due to flammability violation

    Duluth Trading recalls about 22,400 children's holiday pajama sets that violate federal flammability regulations for sleepwear, posing a risk of burn injuries to children.

    Product
    Children's Holiday Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25106·2025-01-23

    Teckwe Hair Dryer Brushes Recalled for Electrocution and Shock Hazard

    SHEIN Distribution is recalling about 310 Teckwe hair dryer brushes because they lack immersion protection, posing an electrocution or shock hazard if they fall into water while plugged in. No injuries have been reported.

    Product
    Teckwe Hair Dryer Brushes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25103·2025-01-23

    NQDTPBOR Multi-Purpose Helmets Recalled Due to Head Injury Risk

    NQDTPBOR multi-purpose helmets for teens do not comply with federal bicycle safety standards for impact protection, stability, labeling, and certification. The recalled helmets, sold on Amazon from May to August 2024, can fail to protect wearers in a crash.

    Product
    NQDTPBOR Multi-Purpose Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V032000·2025-01-23

    Acura MDX touchscreen can go blank hiding the rearview camera

    Honda is recalling certain 2025 Acura MDX vehicles because the centre console touchscreen may go blank, so the rearview camera image does not display. This fails FMVSS 111.

    Product
    ACURA — ACURA MDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0830-2025·2025-01-22

    Impella RP Flex Devices Recalled Due to Optical Sensor Damage Risk

    Abiomed is recalling 2,364 units of the Impella RP Flex with SmartAssist due to risk of optical sensor damage from device interaction. Damage may cause temporary or permanent pump stop and loss of vital monitoring signals.

    Product
    Impella RP Flex with SmartAssist; Product Number: 1000323;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0884-2025·2025-01-22

    Welch Allyn Life 2000 Ventilator Battery Charger Defect Causes Inoperability

    The Welch Allyn Life 2000 Ventilator has a battery charger defect that could cause an alarm, rendering it inoperable. 187 units nationwide are affected in this FDA Class I recall.

    Product
    Welch Allyn, Inc., Life 2000 Ventilation System, REF BT-20-0002
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0825-2025·2025-01-22

    ALTRUA 2 DR Pacemaker Models S702 and S722 Safety Mode Risk

    Boston Scientific ALTRUA 2 DR Pacemakers may unexpectedly enter Safety Mode during normal operation due to high battery impedance, potentially affecting device functionality.

    Product
    ALTRUA 2 DR Pacemaker, SL (Model Number S702) and EL (Model Number S722)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0887-2025·2025-01-22

    Life2000 Ventilation System battery charger defect causes device inoperability

    Baxter Healthcare is recalling the Life2000 Ventilation System due to a battery charger defect that can trigger an alarm, rendering the ventilator inoperable and unable to support patients' breathing.

    Product
    Breathe Technologies, Inc., Life2000 Ventilation System, REF BT-20-0002AP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0388-2025·2025-01-22

    Small Veggie Platter Recalled for Potential Salmonella Contamination

    The Kroger Co is recalling Small Veggie Platters (32 oz) because they may contain cut cucumbers previously recalled due to potential Salmonella contamination.

    Product
    SMALL VEGGIE PLATTER, 32 oz., packaged in a plastic container with a plastic lid, UPC 41573-26809
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Devices)·Z-0826-2025·2025-01-22

    CRT-P Pacemakers Recalled for Potential Safety Mode Initiation Risk

    Boston Scientific's ACCOLADE Family pacemakers, including VALITUDE CRT-P models, are recalled due to battery impedance defects that could trigger unintended Safety Mode during normal operation.

    Product
    VALITUDE CRT-P, EL (Model Number U125) and EL MRI (Model Number U128)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0389-2025·2025-01-22

    Boar's Head hummus vegetable platter recalled for Salmonella contamination

    Boar's Head hummus platters are recalled because they may contain cucumbers previously recalled for potential Salmonella contamination. Products were distributed across multiple states.

    Product
    BOAR'S HEAD HUMMUS VEG PLATTER SM, 2.5 lb., packaged in a plastic container with a plastic lid, UPC 42421-61545
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Devices)·Z-0829-2025·2025-01-22

    Impella RP Heart Pump Recalled Due to Optical Sensor Damage Risk

    Abiomed is recalling 1,560 units of the Impella RP with SmartAssist pump due to risk of optical sensor damage from device interactions. Damaged sensors may cause temporary or permanent pump malfunction.

    Product
    Impella RP with SmartAssist; Product Number: 0046-0035;
    Category
    Medical Device
    Distribution
    Distributed nationwide