The Recall Desk

State

Texas product recalls

73,495 recalls have nationwide distribution and so reach Texas. 12,437 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total
12,437
Critical
1,720
Severe
2,926
Most recent
2026-10-14

Of the 12,437 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 12,437 recalls whose distribution notice names Texas specifically. The 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24576–24600 of 85932

  • CriticalFDA (Food)·F-0815-2022·2022-03-09

    Vadilal Quick Treat Custard Apple Pulp Recalled for Salmonella

    Vadilal Industries is recalling Quick Treat Custard Apple Pulp (1kg packages, UPC 8901777282168) due to potential Salmonella contamination. Approximately 997 cases were distributed nationwide to retail stores.

    Product
    Vadilal Quick Treat Custard Apple Pulp Net Wt, 1kg/35.27-oz. Product code FPEP44302 UPC:8901777282168 Best Before September 2023
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0680-2022·2022-03-09

    Celltrion DiaTrust COVID-19 Rapid Test Kits Recalled for Unauthorized Clinical Use

    Celltrion USA recalled COVID-19 rapid test kits (DiaTrust) in a Class I action. The kits are labeled for research use only, but the firm assured distributors they could be used for clinical diagnosis, which is not authorized.

    Product
    Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0663-2022·2022-03-09

    Philips Respironics V60 Plus Ventilators with Defective Adhesive Recalled

    Respironics California is recalling 294 V60 Plus ventilators assembled with expired adhesive. The adhesive may fail, causing the bracket to loosen and damage capacitors, potentially stopping ventilation delivery.

    Product
    Philips Respironics V60 Plus Ventilator Part Number 1138747
    Category
    Medical Device
    Distribution
    13 states
  • SevereNHTSA·22V139000·2022-03-09

    Maintainer Recalls 2021-2022 Crane Trucks Due to Fire Risk

    Maintainer is recalling 2021-2022 crane-equipped truck bodies because an inductor may contact the frame, causing an electric arc and increasing fire risk.

    Product
    MAINTAINER — MAINTAINER CRANE W/ SERVICE BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0662-2022·2022-03-09

    Philips V60 Ventilator Recall: Expired Adhesive May Cause Device Failure

    A limited number of Philips Respironics V60 ventilators were assembled with expired adhesive. If the adhesive fails, the ventilator could stop providing ventilation.

    Product
    Philips Respironics V60 Ventilator Part Number 1053617
    Category
    Medical Device
    Distribution
    13 states
  • SevereFDA (Food)·F-0813-2022·2022-03-09

    Enoki Mushrooms Recalled Due to Listeria monocytogenes Contamination Risk

    GOLDEN MEDAL MUSHROOM INC is recalling Xuerong brand enoki mushrooms contaminated with Listeria monocytogenes. The affected product was distributed in California, Texas, and Illinois.

    Product
    Enoki Mushrooms, brand Xuerong, net wt. 150 g/ 5.25200g/7.05-ounce packages, UPC 6953150110157. 34 0er carton.
    Category
    Food
    Distribution
    3 states
  • SevereCPSC·22094·2022-03-09

    Olight M2R Pro and Warrior Mini Flashlights Recalled for Burn Hazard

    Olight is recalling about 215,100 M2R Pro and Warrior Mini flashlights because they can turn on accidentally and overheat while stored in a holster or pocket, creating a burn hazard. The company has received 127 reports of unintended activation with 22 burn injuries, including three second-degree burns.

    Product
    M2R Pro and Warrior Mini Flashlights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0720-2022·2022-03-09

    BUTLER Clear Dip Recalled for Lack of FDA Premarket Clearance

    Sunstar Americas is recalling BUTLER Clear Dip nationwide due to lack of FDA premarket clearance. The product was distributed in 22,514 units across multiple lot codes.

    Product
    BUTLER Clear Dip, 12 bottles/case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0689-2022·2022-03-09

    Titanium Toe Joint Implant Labeling Error: Unvalidated MRI Safety Claims

    BioPro Titanium MPJ toe implants are recalled due to false documentation claiming MRI safety testing that was never performed. Patients should not undergo MRI with this implant until properly evaluated.

    Product
    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC LG, Part ID 17038
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0721-2022·2022-03-09

    Surgical knee navigation implant recalled over sterilization failures

    Orthosoft's NavitrackER knee navigation system may lack proper sterilization. The product was distributed without passing required sterilization tests, risking infection.

    Product
    NavitrackER Kit A: Knee, Model Number 20-8000-000-07,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0688-2022·2022-03-09

    Titanium Toe Joint Implant Contains False MR Compatibility Claims

    BioPro recalled titanium toe implants due to incorrect claims in documentation about magnetic resonance (MR) compatibility testing that was never conducted. The FDA issued a Class II recall to address the misleading safety information.

    Product
    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC M/L, Part ID 17037
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0655-2022·2022-03-09

    Digital Angiography System generator may exceed safe radiation dose rates

    Shimadzu recalled 28 Digital Angiography Systems with Generator Model D150GC-40 due to inadequate installation adjustment criteria that may cause x-ray radiation dose rates to exceed safe fluoroscopic imaging limits.

    Product
    Digital Angiography System Shimadzu Trinias Generator Model: D150GC-40
    Category
    Medical Device
    Distribution
    15 states
  • HighFDA (Devices)·Z-0699-2022·2022-03-09

    Helix Elite Molecular Reference Standard Recall for Failed Shelf-Life Testing

    Microbiologics Inc is recalling Helix Elite Molecular Standards for inactivated RSV A because real-time shelf life testing failed at 24 months, indicating the product may not maintain stability through its claimed expiration date.

    Product
    Helix Elite" Molecular Standards: Inactivated Standard. Inactivated Respiratory Syncytial Virus A Strain Long. Target pathogens are lyophilized in a PCR compatible matrix, and stable at 2¿C-25¿C through the expiration date. Each lyophilized pellet is packaged in a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0712-2022·2022-03-09

    KWIK-STIK Quality Control Kit Recalled for Incorrect Antibiotic Susceptibility

    Microbiologics Inc is recalling KWIK-STIK quality control kits containing Enterococcus faecalis because certain lots are susceptible to Gentamicin Synergy when they should be resistant. The defect could affect laboratory testing accuracy.

    Product
    KWIK-STIK, Quality control kit for culture media, sold as: a. KWIK-STIK 2-pack Enterococcus faecalis derived from ATCC 51299 b. KWIK-STIK 6-pack Enterococcus faecalis derived from ATCC 51299
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0715-2022·2022-03-09

    Stryker medical implant recalled for manufacturing defect in barrier layer

    Stryker is recalling MEDPOR Titan OFW implants after one unit was found with an incorrectly placed barrier layer. The defect resulted from manufacturing error rather than design.

    Product
    MEDPOR Titan OFW - MTB - Right - 1.0mm, Catalog number 81032
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0710-2022·2022-03-09

    Abbott Alinity m reaction units risk detachment during transport

    Abbott Molecular is recalling 3063 kits of Alinity m Integrated Reaction Units due to potential detachment of reaction vessels from the unit cap during transport. No injuries have been reported.

    Product
    Alinity m Integrated Reaction Units (IRU)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0702-2022·2022-03-09

    da Vinci Surgical Cannula Reducer Metal Tip May Dislodge During Surgery

    Intuitive Surgical is recalling the da Vinci Xi and X 12-8 mm Conductive Cannula Reducer because the metal tip may dislodge from the plastic shaft. If unnoticed, additional surgery may be needed, or energy leakage could cause tissue damage.

    Product
    da Vinci Xi and X 12-8 mm Conductive Cannula Reducer, REF: 470381-11
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0686-2022·2022-03-09

    Titanium Toe Implants Recalled for Incorrect MRI Safety Labeling

    BioPro Titanium MPJ toe implants are recalled because labeling incorrectly claims MRI safety without actual testing. Patients should consult their physician before undergoing MRI procedures.

    Product
    Titanium MPJ (Toe Implant)TOE JOINT TITANIUM PC SM, Part ID 17035
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0691-2022·2022-03-09

    Titanium MPJ Toe Implant Recalled for Incorrect MR Safety Labeling

    BioPro is recalling Titanium MPJ toe implants (Lot 125651) with inaccurate labeling claiming MR compatibility when the implant has not been tested for magnetic resonance safety. Patients should consult their physician before MRI.

    Product
    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MS, Part ID 17198
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0681-2022·2022-03-09

    Acorn stairlifts recalled due to inadequate seat structural strength

    Acorn Stairlifts Inc. is recalling multiple stairlift models because the seats may not have adequate strength to consistently support users during continued use, creating a fall hazard.

    Product
    Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0700-2022·2022-03-09

    Helix Elite Molecular Standard Fails FDA Shelf-Life Stability Testing

    Microbiologics Inc. recalls Helix Elite Inactivated Neisseria gonorrhoeae Strain GL0071 molecular standard after real-time shelf life testing failed at 24 months. The product was distributed nationwide and internationally.

    Product
    Helix Elite" Molecular Standards: Inactivated Standard. Inactivated Neisseria gonorrhoeae Strain GL0071.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22096·2022-03-09

    Honda Talon 1000 ROVs recalled for engine failure and crash risk

    Honda is recalling approximately 32,000 Talon 1000 recreational off-highway vehicles from 2019-2021 because a loose intake funnel band screw can enter the engine and cause sudden failure, potentially leading to loss of control and crashes.

    Product
    Honda Talon 1000 ROVs
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0687-2022·2022-03-09

    Titanium Toe Implant Recalled for Incorrect MRI Safety Claims

    BioPro Titanium MPJ toe implant documentation incorrectly claims MRI safety testing that was never conducted. The implant is not proven safe for MRI use.

    Product
    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MD, Part ID 17036
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0690-2022·2022-03-09

    Titanium Toe Implant Recalled for Incorrect MRI Safety Statements

    BioPro is recalling Titanium MPJ toe implants due to false claims of MRI compatibility. The device instruction manual states it is MRI-safe despite not being tested.

    Product
    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MS, Part ID 17197
    Category
    Medical Device
    Distribution
    Distributed nationwide