The Recall Desk

State

Texas product recalls

73,381 recalls have nationwide distribution and so reach Texas. 12,434 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total
12,434
Critical
1,720
Severe
2,926
Most recent
2026-10-07

Of the 12,434 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 12,434 recalls whose distribution notice names Texas specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20701–20725 of 85815

  • HighFDA (Devices)·Z-0342-2023·2022-12-07

    CMV IgM EIA Diagnostic Test Recalled for Increased False Positives

    Bio-Rad Laboratories is recalling 180 CMV IgM EIA diagnostic test kits due to unusually high rates of false positive results. The recall affects test kits distributed in 14 U.S. states.

    Product
    CMV IgM EIA, in vitro diagnostic.
    Category
    Medical Device
    Distribution
    14 states
  • HighNHTSA·22V902000·2022-12-07

    Nova Bus Recalls LFS Models for Non-Standard Auxiliary Lighting

    Nova Bus is recalling 2009-2021 LFS and LFS Artic transit buses because non-standard color auxiliary lights may distract other drivers and increase crash risk.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0072-2023·2022-12-07

    FDA recalls prescription desmopressin acetate tablets for subpotency

    Heritage Pharmaceuticals' desmopressin acetate tablets (0.2mg) have been recalled nationwide due to subpotency. The voluntary recall affects 13,805 bottles; no illnesses have been reported.

    Product
    DESMOPRESSIN ACETATE — DESMOPRESSIN ACETATE (DESMOPRESSIN ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0071-2023·2022-12-07

    Daytrana transdermal methylphenidate patches recalled for adhesive defect

    Noven Pharmaceuticals recalls 3,977 boxes of Daytrana methylphenidate transdermal patches nationwide due to defective adhesive properties in lot 91316. Affected patches may fail to adhere properly or deliver medication inconsistently.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0179-2023·2022-12-07

    Coolhaus Dairy Free Frozen Dessert Recalled for Coliform Detection

    Coolhaus Dairy Free Cookie Dough Lyfe frozen dessert sandwiches recalled due to coliform detected in lab samples. Product distributed to select retailers in Texas, Maryland, Colorado, and California.

    Product
    Coolhaus Dairy Free Cookie Dough Lyfe Frozen Dessert Sandwich 3 pk units - 8.75 oz (2.9 oz./unit) UPC: 8 5000988328 5 Distributed by Coolhaus 8688 Washington Blvd. Culver City, CA 90232
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0353-2023·2022-12-07

    Laboratory Diagnostic Probe Recalled for Incorrect Chromosome Map Labeling

    Cytocell Ltd. recalls CytoCell BCL11B Proximal probe used in T-cell malignancy testing (lot RD22/230/10). The package insert contains an incorrect chromosome map that doesn't match the probe design.

    Product
    CytoCell BCL11B Proximal in FITC Spectrum-LDT for investigation T-cell related malignancy. This device is an analyte specific reagent probe covering the 14q32.2 locus proximal to the BCL11B gene on chromosome 14. Ref: MPD39781
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0326-2023·2022-12-07

    Surgical Injection Tray Recalled Due to Adhesive Liner Defect

    Busse Hospital Disposables is recalling 40 cases of Busse Spine Injection Trays containing 3M Steri-Drape Surgical Drapes distributed in Texas due to a defective adhesive liner that is difficult to remove without damaging the product.

    Product
    Busse SPINE INJECTION TRAY-Intended as a nerve block REF No. 8563R1
    Category
    Medical Device
    Distribution
    1 state
  • ModerateNHTSA·22V901000·2022-12-07

    Audi Recalls 2023 S3, RS3, and A3 for Missing Weight Label

    Volkswagen Group of America is recalling 2023 Audi S3, RS3, and A3 vehicles because the B-pillar safety label is missing weight capacity information.

    Product
    AUDI — AUDI S3, RS 3, A3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0074-2023·2022-12-07

    Acella Recalls Sodium Sulfacetamide Cleansing Pads for Subpotency

    Acella Pharmaceuticals is recalling Sodium Sulfacetamide 10% Sulfur 4% Cleansing Pads because testing found the drug out of specification for potency at shelf-life expiration. 528 cartons distributed nationwide are affected.

    Product
    Sodium Sulfacetamide 10% Sulfur 4% Cleansing Pads, Net weight 3.7g (60 cleansing pads Net weight 3.7 g each per carton,) Rx Only, Manufactured For: Acella Pharmaceuticals, LLC Alpharetta, GA 300025, NDC 42192-113-60
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0073-2023·2022-12-07

    Allergy Relief D tablets recalled for failed dissolution specifications

    Dr. Reddy's Laboratories is recalling Allergy Relief D extended-release tablets distributed nationwide by Walmart due to failed dissolution specifications. No illnesses or injuries have been reported.

    Product
    Allergy Relief D, Fexofenadine HCL 60mg/Antihistamine, Pseudoephedrine HCL 120mg/Nasal Decongestant, Extended-Release Tablets USP, packaged as (a) 20 count carton NDC 49032-273-20; (b) 30 count carton, NDC49032-273-30; Distributed by: Walmart Inc., Bentonville, AR 72716, Product…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0325-2023·2022-12-07

    3M Steri-Drape Surgical Drapes Recalled Due to Adhesive Liner Defect

    3M is recalling Steri-Drape Surgical Drapes because the liner on the adhesive component is difficult to remove without damaging the product, potentially rendering it unusable.

    Product
    Busse JOINT INJECTION TRAY -Intended as a nerve block REF No. 8561 R1
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0341-2023·2022-12-07

    BCL11B Diagnostic Reagent Recalled for Chromomap Documentation Error

    Cytocell Ltd. is recalling a diagnostic reagent due to an error in the chromomap on the package insert. The nucleotide locations in the text are correct, but the chromosome map was created using incorrect coordinates.

    Product
    CytoCell BCL11B Distal in Texas Red Spectrum- Analyte Specific Reagent Ref: MPD39782
    Category
    Medical Device
    Distribution
    1 state
  • SevereNHTSA·22V899000·2022-12-06

    Kia Recalls 2020 Niro EV Vehicles for EPCU Coolant Leak Risk

    Kia is recalling 2020 Niro EV vehicles because a coolant leak in the Electric Power Control Unit may cause loss of drive power, increasing crash risk.

    Product
    KIA — KIA NIRO EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V898000·2022-12-06

    Hino Recalls 2022-2023 Trucks Due to Fuel Pickup Tube Defect

    Hino is recalling 970 specific 2022-2023 models because a fuel tube may restrict fuel flow, potentially causing engine stalls and increasing crash risk.

    Product
    HINO — HINO NJ7A, NJ7B, NV7A, NE7A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V900000·2022-12-06

    KTM 1290 Super Duke R Motorcycles Recalled for Electrical Wiring Defect

    KTM is recalling 2020-2022 1290 Super Duke R motorcycles because the main wiring harness may be misrouted or missing parts, potentially causing an electrical short-circuit and engine stall.

    Product
    KTM — KTM 1290 SUPER DUKE R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V896000·2022-12-06

    Volvo Recalls 2022-2023 VNL Vehicles for Air Tank Bracket Defect

    Volvo Trucks is recalling certain 2022-2023 VNL vehicles because excessively tightened air tank bracket fasteners may break, allowing the air tank to detach and become a road hazard.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V895000·2022-12-05

    Tesla Recalls 2023 Model Y Vehicles for Suspension Fastener Defect

    Tesla is recalling 2023 Model Y vehicles because front suspension fasteners may not be properly attached, which could cause instability and increase crash risk.

    Product
    TESLA — TESLA MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22T022000·2022-12-05

    Continental Tire Recalls Specific Models Due to Sidewall Break Risk

    Continental Tire is recalling specific 4x4 Contact, PureContact LS, and TerrainContact H/T tires because overcuring may cause sidewall breaks or tread separation, increasing crash risk.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-12052022-001·2022-12-05

    Ground Beef Alert Issued for E. Coli O157:H7 Contamination at Texas Store

    USDA FSIS issued a public health alert for ground beef sold at La Michoacana Meat Market in Greenville, Texas, after testing positive for E. coli O157:H7.

    Product
    FSIS Issues Public Health Alert for Ground Beef Products That Tested Positive for E. Coli O157:H7
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·22V894000·2022-12-05

    Old School Trailers Recalls 2022 Models Due to Awning Seam Defect

    Old School Trailers is recalling 2022 models because a welded seam on the electric retractable awning may separate, causing the awning to drop and increasing injury risk.

    Product
    OLD SCHOOL TRAILERS — OLD SCHOOL TRAILERS OLD SCHOOL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V893000·2022-12-02

    Terex Recalls 2022 Aerial Work Platforms Due to Boom Weld Defect

    Terex is recalling 431 units of 2022 C4000, C5000, C6000, C7000, General, and TL vehicles because a seam in the boom structure may have been improperly welded.

    Product
    TEREX — TEREX C5000, TL, C4000, C7000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V892000·2022-12-02

    Pierce Recalls 2022 Fire Trucks Due to Tie Rod Clamp Cracking

    Pierce Manufacturing is recalling 2022 Saber, Enforcer, and Arrow XT fire trucks because improperly heat-treated tie rod clamps may crack, risking sudden loss of steering.

    Product
    PIERCE — PIERCE ENFORCER, ARROW XT, SABER
    Category
    Vehicle
    Distribution
    Distributed nationwide