The Recall Desk

State

Texas product recalls

73,596 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
1,716
Severe
2,930
Most recent
2026-10-21

Of the 12,438 recalls naming Texas we have scored against our rubric, 1,716 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,930 (24%) are Severe.

Which agencies issued them

These figures cover only the 12,438 recalls whose distribution notice names Texas specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

651–675 of 86034

  • ModerateFDA (Devices)·Z-3188-2026·2026-09-23

    Boston Scientific StoneSmart Connect Console Power Adapter Recall

    Boston Scientific is recalling StoneSmart Connect Console power adapters that may fail electrical safety testing due to high grounding resistance.

    Product
    Boston Scientific Corporation StoneSmart Connect Console Contents: (1) Power Cord, (1) Power Adaptor, (1)DVI Cable, (1) DVI to HDMI Cable, (1) DisplayPort Cable REF: M0067933000, M006793300H0, M006793300R0, M006793300D0, M006793300Z0, M0067930000, M006793000R0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3172-2026·2026-09-23

    SunMed Tracheal Tube Recalled Due to Suction Catheter Passage Issues

    Well Lead Medical Co. Ltd is recalling SunMed Tracheal Tubes because a 6Fr suction catheter could not pass through the samples smoothly.

    Product
    SunMed Tracheal Tube, Size 2.5; Model Number: 1-7333-25
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0842-2026·2026-09-23

    Safecor Health Recalls Fluphenazine HCl Elixir Due to Stability Failures

    Safecor Health is recalling Fluphenazine HCl Elixir because it failed stability specifications. The product is distributed nationwide.

    Product
    Fluphenazine HCl Elixir, USP, 5 mg per 1 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use Only, Rx Only, Pkg by: Safecor Health, Woburn, MA 01801. NDC: 00121-0653-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3157-2026·2026-09-23

    ICU Medical Recalls IV Administration Sets with Drip Chamber Specks

    ICU Medical is recalling IV Non-Dedicated Gravity Administration Sets because black specks in the drip chamber may cause healthcare providers to delay therapy.

    Product
    IV Non-Dedicated Gravity Administration Sets with drip chambers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3180-2026·2026-09-23

    Embecta Medical Recalls Pen Needles Labeled for Investigational Use Only

    Embecta Medical II LLC is recalling pen needles labeled 'For Investigational Use Only' that were inadvertently distributed as commercially marketed devices.

    Product
    EWO_02513 (Catalog number 320122) For Investigational Use Only Nano Un-Cannulated Demo Samples Quantity 100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0844-2026·2026-09-23

    Safecor Health Recalls Fluphenazine HCl Elixir Due to Stability Failures

    Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product is distributed nationwide.

    Product
    Fluphenazine HCl Elixir, USP, 10 mg per 2 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use Only, Rx Only, Pkg by: Safecor Health, Woburn, MA 01801. NDC: 00121-0653-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3158-2026·2026-09-23

    ICU Medical Recalls Oncology Sets with Drip Chamber Discoloration

    ICU Medical is recalling 107,800 oncology sets because drip chambers may contain black specks from the molding process, which could lead to product replacement and therapy delays.

    Product
    Oncology sets with drip chambers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0846-2026·2026-09-23

    Safecor Health Recalls Fluphenazine HCl Elixir Due to Stability Failures

    Safecor Health is recalling Fluphenazine HCl Elixir because it failed stability specifications. The product was distributed nationwide in the USA.

    Product
    Fluphenazine HCl Elixir, USP, 20 mg per 4 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use Only, Rx Only, Pkg by: Safecor Health, Woburn, MA 01801. NDC: 00121-0653-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3159-2026·2026-09-23

    ICU Medical Recalls Oncology Sets with Potential Drip Chamber Discoloration

    ICU Medical is recalling 28,550 oncology sets because drip chambers may contain black specks from the molding process. The discolored material does not enter the fluid path but may cause therapy delays.

    Product
    Oncology sets with drip chambers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0843-2026·2026-09-23

    Safecor Health Recalls Fluphenazine HCl Elixir Due to Stability Failures

    Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product is distributed nationwide in the USA.

    Product
    Fluphenazine HCl Elixir, USP, 5 mg per 10 mL, Delivers: 10 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use Only, Rx Only, Pkg by: Safecor Health, Woburn, MA 01801. NDC: 00121-0654-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0841-2026·2026-09-23

    Safecor Health Recalls Fluphenazine HCl Elixir Due to Stability Failures

    Safecor Health is recalling specific lots of Fluphenazine HCl Elixir because they failed stability specifications. The product was distributed nationwide.

    Product
    Fluphenazine HCl Elixir, USP, 2.5 mg per 5 mL, Delivers: 5 mL, Oral Elixir, PAI, Alcohol 14% by volume, For Oral Use Only, Rx Only, Pkg by: Safecor Health, Woburn, MA 01801. NDC: 00121-0654-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·022-2026·2026-09-22

    Star Meat Delivery Recalls Raw Pork, Beef, and Goat Products

    Star Meat Delivery Inc. is recalling raw pork, beef, and goat products produced without federal inspection and bearing false USDA marks.

    Product
    Star Meat Delivery Inc. Recalls Raw Pork, Beef, and Goat Products Produced Without the Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V604000·2026-09-22

    Nova Bus Recalls 2024-2025 LFS Transit Buses for Parking Brake Defect

    Nova Bus is recalling 2024-2025 LFS transit buses because an improperly tightened emergency brake valve may cause air leaks and unintentional parking brake activation.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E065000·2026-09-22

    Ford Recalls 2024-2026 Ranger Vehicles for Rearview Camera Display Failure

    Ford is recalling 2024-2026 Ranger vehicles with 10.1-inch center stack screens that may lose power and fail to display the rearview camera image, increasing crash risk.

    Product
    BACK OVER PREVENTION:DISPLAY FUNCTION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V606000·2026-09-22

    Ford Recalls 2025-2027 Vehicles for Contaminated Headlight LED Chips

    Ford is recalling specific 2025-2027 Expedition and F-Series Super Duty vehicles because contaminated LED chips in the headlights may cause a loss of exterior lighting, increasing crash risk.

    Product
    FORD — FORD F-550 SD, EXPEDITION, F-250 SD, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V605000·2026-09-22

    Ford Recalls 2026 Rangers for Rearview Camera Display Failure

    Ford is recalling 2026 Ranger vehicles because the center screen may lose power, preventing the rearview camera image from displaying and increasing crash risk.

    Product
    FORD — FORD RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V603000·2026-09-21

    Forest River Recalls 2026-2027 Dynamax Grand Sport GT Recreational Vehicles

    Forest River is recalling 2026-2027 Dynamax Grand Sport GT recreational vehicles because an improperly installed engine pre-heat pump may cause coolant hose failure and engine overheating.

    Product
    DYNAMAX — DYNAMAX GRAND SPORT GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V600000·2026-09-18

    Volvo Bus 9700 Recall for Missing Emergency Exit Instructions

    Volvo Bus is recalling 2009-2025 9700 buses because the emergency exit label on the entrance door is missing operating instructions, which may delay evacuation.

    Product
    VOLVO BUS — VOLVO BUS 9700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26779·2026-09-17

    LANCHEZ Pressure Washers Recalled for Shock and Electrocution Hazards

    LANCHEZ pressure washers are recalled because they lack a ground-fault circuit-interrupter and adequate power cord, posing risks of shock or electrocution.

    Product
    LANCHEZ Pressure Washers
    Category
    Consumer Product
    Distribution
    Distributed nationwide