The Recall Desk

State

Texas product recalls

73,213 recalls have nationwide distribution and so reach Texas. 12,431 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total
12,431
Critical
1,720
Severe
2,423
Most recent
2026-10-06

Of the 12,431 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 2,423 (19%) are Severe.

These figures cover only the 12,431 recalls whose distribution notice names Texas specifically. The 73,213 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15576–15600 of 85644

  • HighFDA (Devices)·Z-0208-2024·2023-11-08

    POC Analyzer Risk of Erroneous Creatinine Results During Cartridge Startup

    Nova Biomedical's Stat Profile Prime Plus POC analyzer may report inaccurate creatinine results during the first 2-4 hours after sensor cartridge installation. Standard quality control checks may not detect these errors.

    Product
    Nova Stat Profile Prime Plus POC Analyzer (CE)-Intended to measure certain gases in blood, serum, plasma or pH of blood, serum, and plasma. (1) PN 63368 Stat Profile Prime Plus POC Analyzer (2) PN 63369 Stat Profile Prime Plus POC Analyzer, Remanufactured P/N: 57400…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0081-2024·2023-11-08

    Gynazole 1 Butoconazole Vaginal Cream Recalled for Formulation Error

    Padagis US LLC is recalling Gynazole 1 butoconazole nitrate vaginal cream nationwide due to a manufacturing error where hydrophilic colloidal silica was used instead of hydrophobic colloidal silica.

    Product
    GYNAZOLE 1 — GYNAZOLE 1 (BUTOCONAZOLE NITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0216-2024·2023-11-08

    Cepheid Xpert Xpress Strep A test kits may produce invalid results

    Cepheid is recalling 1,413 Xpert Xpress Strep A test kits due to a defect in the included pipettes. Defective pipettes may fail to dispense adequate sample volume, resulting in invalid test results or no test result.

    Product
    Xpert Xpress Strep A, REF:Xprstrepa-CE-10, CE IVD,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0080-2024·2023-11-08

    Opium Tincture recalled for subpotent morphine content nationwide

    Edenbridge Pharmaceuticals recalled opium tincture nationwide because the morphine concentration fell below labeled potency. The voluntary recall affected 4,548 bottles.

    Product
    OPIUM TINCTURE DEODORIZED — OPIUM TINCTURE DEODORIZED (MORPHINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0085-2024·2023-11-08

    Bisoprolol Fumarate and Hydrochlorothiazide Tablets Recalled for Failed Quality Specifications

    Glenmark Pharmaceuticals is recalling Bisoprolol Fumarate and Hydrochlorothiazide Tablets due to failed impurities and degradation specifications. The recall affects 480 bottles distributed nationwide.

    Product
    BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE — BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE (BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0212-2024·2023-11-08

    Hillrom Progressa+ Hospital Beds Recalled for Static Electricity Risk

    Hillrom Progressa+ hospital beds (499 units) are being recalled due to potential static electricity buildup that could cause mild shock to operators during transport. The affected units were distributed nationwide.

    Product
    HILLROM PROGRESSA+ BED, Product Codes: P7501A000016, P7501A000019, P7501A000031, P7501A000032, P7501A000033, P7501A000052, P7501A000053, P7501A000054, P7501A000055, P7501A001851, P7501A001972, P7501A001973, and P7501A001974
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0204-2024·2023-11-08

    Coapt ControlSeal Electrode Recalled Due to Burn and Blistering Risk

    Coapt LLC is recalling 109 ControlSeal Electrodes due to risk of minor burns or blistering if exposed to direct sunlight or warm temperatures exceeding 12 hours, or if the battery is damaged.

    Product
    Coapt ControlSeal Electrode, cutaneous EMG Electrode
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0217-2024·2023-11-08

    DBS Lead Device Recall: Use By Date Label Discrepancy

    Medtronic is recalling a small number of LEAD 3387S-40 deep brain stimulation devices due to discrepancies in the Use By Date printed on the outer package versus the individual product label.

    Product
    LEAD 3387S-40 STIMLOC DBS, Model Number 3387S-40. Electrical implantable device.
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0197-2024·2023-11-08

    Quest Medical Recalls Q2 Multiport Intravenous Extension Sets

    Quest Medical is recalling 17,700 Q2 Multiport Extension Sets distributed in the US and Canada. The nature of the defect is not detailed in available source documentation.

    Product
    Q2 Multiport Extension set, REF: 9520, Rx Only Sterile, single use non-pyrogenic intravenous fluid administration sets with a multiport IV manifold and integrated back-check valves, pre-attached needleless injection sites, drip chamber and roller clamps.
    Category
    Medical Device
    Distribution
    19 states
  • ModerateFDA (Devices)·Z-0210-2024·2023-11-08

    Endoscopic Vessel Harvesting System Recalled for Incorrect Outer Box Packaging

    Vasoview 6 Pro endoscopic vessel harvesting systems were packaged in incorrect outer boxes displaying artwork for a different device (Vasoview Hemopro 2). The inner labels and product documentation are correct.

    Product
    Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System, Model VH-2400 printed on outer label, inner label and IFU, outer box artwork for Vasoview Hemopro 2 (HP2).
    Category
    Medical Device
    Distribution
    13 states
  • ModerateFDA (Devices)·Z-0205-2024·2023-11-08

    Pediatric Tracheostomy Tube Recalled Due to Incorrect Box Expiration Date Label

    Smiths Medical recalls a pediatric tracheostomy tube because the outer box shows an incorrect expiration date (3/17/2021) while the actual product has the correct date (3/17/2026). The discrepancy could cause confusion about product validity.

    Product
    Smiths Medical Portex Bivona Pediatric Tracheostomy Tube, Cuffless, Model 60P045, Sterile.
    Category
    Medical Device
    Distribution
    18 states
  • ModerateFDA (Drugs)·D-0082-2024·2023-11-08

    Iodine Solution Recalled for Manufacturing Compliance Deviations

    Safecor Health recalls Strong Iodine Solution nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The prescription product was distributed in multiple lots across the U.S.

    Product
    STRONG IODINE SOLUTION — STRONG IODINE SOLUTION (STRONG IODINE SOLUTION)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V748000·2023-11-07

    Alexis Fire Equipment Recalls Fire Apparatus Due to Parking Brake Defect

    Alexis Fire Equipment is recalling 2021-2024 Fire Apparatus vehicles because a defect in the inversion valve may delay parking brake engagement, increasing the risk of unintentional vehicle movement.

    Product
    ALEXIS FIRE EQUIPMENT — ALEXIS FIRE EQUIPMENT FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V746000·2023-11-07

    Mack Recalls 2024 MD Trucks Due to Steering Wheel Bolt Issue

    Mack Trucks is recalling 2024 MD trucks because the steering wheel attachment bolt may loosen and separate, potentially causing the steering wheel to detach.

    Product
    MACK — MACK MD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E086000·2023-11-07

    Cruise Recalls 950 Vehicles for Automated Driving System Software Defect

    Cruise LLC is recalling 950 vehicles because a software defect in the Collision Detection Subsystem may cause the vehicle to move after a crash.

    Product
    ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V747000·2023-11-07

    Spartan Fire Emergency Vehicles Recalled for Parking Brake Defect

    Custom Fire Apparatus is recalling 2021-2024 Spartan emergency vehicles because a parking brake defect may allow unintentional movement, increasing crash risk.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR, FC-94, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V749000·2023-11-07

    Peterbilt Recalls 2024 520 Trucks Due to Engine Bracket Risk

    PACCAR is recalling 2024 Peterbilt 520 vehicles because a rear lifting bracket may detach, posing an injury risk during engine lifting.

    Product
    PETERBILT — PETERBILT 520
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V744000·2023-11-06

    2024 Buick Envista Software Update: Instrument Panel Display Blanking Issue

    General Motors recalls certain 2024 Buick Envista vehicles for a software defect that may cause the instrument panel display to go blank, preventing visibility of critical safety information like vehicle speed and warning lights.

    Product
    BUICK — BUICK, CHEVROLET ENCORE GX, TRAX, ENVISTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·23C005000·2023-11-06

    Evenflo Titan 65 Child Seat Recalled for Missing Warning Labels

    Evenflo is recalling one Titan 65 child seat because it is missing required warning labels, which may increase the risk of injury to the occupant.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V743000·2023-11-03

    Tesla Model S and Model X Incorrect Air Bag Recall

    Tesla is recalling 2021-2024 Model S and Model X vehicles because an incorrect air bag was installed when the steering wheel was replaced. The incompatible air bag could deploy incorrectly during a crash, increasing the risk of injury.

    Product
    TESLA — TESLA MODEL S, MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V739000·2023-11-03

    Forest River Travel Trailers Electrical Wire Gauge Defect Recall

    Forest River is recalling 2023-2024 Sandstorm, Stealth, and 2024 Shockwave travel trailers. The electrical wire from the 50-amp inlet has incorrect gauge and may melt, creating a fire hazard.

    Product
    FOREST RIVER — FOREST RIVER SANDSTORM, STEALTH, SHOCKWAVE
    Category
    Vehicle
    Distribution
    Distributed nationwide