The Recall Desk

State

Texas product recalls

73,509 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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26351–26375 of 85946

  • ModerateFDA (Drugs)·D-0070-2022·2021-11-03

    PainAway II Acetaminophen/Aspirin/Caffeine Tablets Recalled for Failed Stability

    Ultra Seal Corporation is recalling PainAway II tablets nationwide due to failed stability specifications. Testing found out-of-specification levels of Salicylic Acid, an aspirin-related compound.

    Product
    PainAway II (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets , 2 tablets/pk, packaged in 12,000 Packets/Case, Material # 11161, Mfg. for Respond Industries First Aid, Mason, OH 45040 (Shipping Label)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0166-2022·2021-11-03

    GORE CARDIOFORM Septal Occluders Recalled for Incorrect Expiration Date

    W. L. Gore & Associates is recalling GORE CARDIOFORM Septal Occluders labeled with incorrect 3-year expiration dates instead of 2-year dates. This labeling error affects devices distributed across the United States and internationally.

    Product
    REF/Catalogue Number GSX0025A, GORE CARDIOFORM SEPTAL OCCLUDER 25 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132631025 *Not distributed within the US
    Category
    Medical Device
    Distribution
    47 states
  • ModerateFDA (Devices)·Z-0167-2022·2021-11-03

    GORE CARDIOFORM SEPTAL OCCLUDER Recalled for Incorrect Expiration Date Labeling

    GORE CARDIOFORM SEPTAL OCCLUDER devices are recalled for labeling errors: 95 units marked with 3-year expiration instead of correct 2-year date. Affected units distributed across US and international locations.

    Product
    REF/Catalogue Number GSXE0020, GORE CARDIOFORM SEPTAL OCCLUDER 20 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132617630 *Not distributed within the US
    Category
    Medical Device
    Distribution
    47 states
  • LowFDA (Drugs)·D-0072-2022·2021-11-03

    ZEE+ Painaid ESF Tablets Recalled for Failed Stability Specifications

    Ultra Seal Corporation is recalling ZEE+ Painaid ESF Extra-Strength Formula tablets nationwide due to out-of-specification results for Salicylic Acid, an aspirin-related compound. The recall affects 50-count and 125-count packages with lot numbers AK-9547 (exp. April 22) and AK-9941 (exp. December 22).

    Product
    ZEE+ painaid ESF Extra-Strength Formula (Acetaminophen 250 mg, Aspirin 250 mg (NSAID), Caffeine 65 mg) tablets, 2 Tablets per/package, Packaged in a) 50-count packages/carton, b) 125-count packages/carton, PA-ESF 1414Z, Dist. by: Zee Medical Distributors, LLC Mason, OH 45040…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0069-2022·2021-11-03

    Kirkland Signature AllerClear D 24 HR Tablets Recalled for Moisture Failure

    SUN PHARMACEUTICAL INDUSTRIES INC is recalling Kirkland Signature AllerClear D 24 HR (Loratadine and Pseudoephedrine Sulfate) tablets nationwide because the product failed to meet moisture content limits.

    Product
    KIRKLAND SIGNATURE ALLERCLEAR D 24 HR — KIRKLAND SIGNATURE ALLERCLEAR D 24 HR (LORATADINE AND PSEUDOEPHEDRINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0071-2022·2021-11-03

    Vica-Cet Back Pain Relief tablets recalled for stability specification failure

    Ultra Seal Corporation is recalling Vica-Cet Back Pain Relief tablets nationwide because certain lots failed stability testing and contain out-of-specification levels of Salicylic Acid, an aspirin-related compound.

    Product
    Vica-Cet BACK PAIN RELIEF (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets, 2 tablets/pk, packaged in 10,000 packets, PO# 8967, Mfg. for Tellus/The Provision First Aid Line (Shipping Label)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V850000·2021-11-02

    Thomas Built Buses Recalling 2020-2022 Models for Alternator Fire Risk

    Daimler Trucks is recalling 1,434 Thomas Built school buses because a loose alternator cable connection may cause electrical arcing and increase the risk of a fire.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX, SAF-T-LINER EFX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V848000·2021-11-02

    Alfa Romeo Giulia Recalled for Tires with Incorrect Load Rating

    FCA US is recalling 2020 Alfa Romeo Giulia vehicles because some may have tires with a lower load rating than intended, increasing crash risk.

    Product
    ALFA ROMEO — ALFA ROMEO GIULIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V851000·2021-11-02

    Oshkosh Recalls 2020-2021 S-Series Vehicles for Power Steering Defect

    Oshkosh is recalling 2020-2021 S-Series vehicles because a machining defect may cause the power steering pump shaft seal to break, resulting in a loss of steering assist.

    Product
    OSHKOSH — OSHKOSH S-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V849000·2021-11-01

    Heartland Cyclone and Road Warrior RVs recalled for loose electrical wires

    Heartland Recreational Vehicles is recalling 2019-2021 Road Warrior and 2020-2021 Cyclone trailers because wire securement lugs may be improperly tightened. Loose wires can cause electrical arcing and increase fire risk.

    Product
    HEARTLAND — HEARTLAND CYCLONE, ROAD WARRIOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V844000·2021-10-29

    Kia Recalls 2017-2018 Optima Hybrid Vehicles for Engine Bearing Wear

    Kia is recalling 2017-2018 Optima Hybrid and Plug-In Hybrid vehicles because premature engine bearing wear can cause engine damage, increasing the risk of fire or a crash.

    Product
    KIA — KIA OPTIMA HYBRID, OPTIMA PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E092000·2021-10-29

    Windshield Fastener Recall: Axalta Coating Systems Bonding Defect

    Axalta Coating Systems is recalling windshields that may not be adequately bonded to Ford and Chrysler vehicles due to a coating defect.

    Product
    VISIBILITY:WINDSHIELD:CRITICAL FASTENERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V843000·2021-10-29

    Mercedes-Benz Recalls 2021 S 580 for Engine Stall Risk

    Mercedes-Benz is recalling 2021 S 580 and Maybach S 580 vehicles because a software error may cause the engine to stall without restarting, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ S 580
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V845000·2021-10-29

    Thor Motor Coach Recalls 2017 Outlaw, Challenger, and Miramar Motorhomes

    Thor Motor Coach is recalling 2017 Outlaw, Challenger, and Miramar motorhomes because external compartment door skins may separate during transit, creating a road hazard.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH CHALLENGER, MIRAMAR, OUTLAW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-10292021·2021-10-29

    USDA Issues Public Health Alert for Citterio Salame Sticks Due to Salmonella

    USDA FSIS issued a public health alert for Citterio Premium Italian-Style Salame Sticks due to possible Salmonella contamination linked to a multistate outbreak.

    Product
    FSIS Issues Public Health Alert for Salame Stick Products Due to Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V846000·2021-10-29

    Tesla Model 3 Forward Collision Avoidance System Software Error

    Tesla is recalling certain 2017-2021 Model 3, S, X, and Y vehicles due to a software error that may cause false forward-collision warnings or unexpected automatic emergency brake activation. No injuries have been reported.

    Product
    TESLA — TESLA MODEL S, MODEL X, MODEL 3, MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V842000·2021-10-28

    2021 Dodge Durango Rear Spoiler May Detach, Becoming Road Hazard

    Chrysler is recalling 2021 Dodge Durango vehicles because the rear spoiler may not be properly aligned and could detach during liftgate use, creating a road hazard. Dealers will replace the spoiler free of charge.

    Product
    DODGE — DODGE DURANGO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22704·2021-10-28

    Design Within Reach Arc Collection Furniture Recalled for Excess Lead Paint

    Design Within Reach is recalling its Arc Collection furniture (chairs, tables, and barstools) because the surface paint contains lead levels exceeding the federal lead paint ban, posing a risk of lead poisoning to young children.

    Product
    Arc Collection Furniture
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21E091000·2021-10-28

    American Chrome Company Recalls One Piece Hub Cap Kits for Road Hazard Risk

    American Chrome Company is recalling specific One Piece Hub Cap Kits for Volvo and Mack vehicles because a compression spring defect can cause the hubcap to separate, creating a road hazard.

    Product
    WHEELS:HUBCAP/COVER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0010-2022·2021-10-27

    Coppertone Pure & Simple 50 Sunscreen Spray Recalled for Benzene Contamination

    Beiersdorf Inc. is recalling Coppertone Pure & Simple 50 Sunscreen Spray due to the presence of benzene, a chemical contaminant. The recall affects 38,328 cans distributed nationwide.

    Product
    Coppertone Pure & Simple 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02880 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0064-2022·2021-10-27

    Lightly Salted Cashew Halves & Pieces recalled for glass contamination

    Suntree Snack Foods is recalling Lightly Salted Cashew Halves & Pieces (16 oz., UPC 842379195341) due to the presence of glass pieces in the product. The recall affects approximately 4,200 bags distributed across 11 states and Washington, D.C.

    Product
    Lightly Salted Cashew Halves & Pieces, 16 oz., UPC 842379195341. 6 bags/case.
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Food)·F-0020-2022·2021-10-27

    Kalona Supernatural Organic Whipping Cream Recalled for Improper Pasteurization

    Kalona Supernatural Organic Whipping Cream was shipped without proper pasteurization, creating a potential food safety risk. The recall affects 16 FL OZ and 32 FL OZ bottles distributed to retailers in multiple states.

    Product
    Kalona Supernatural Organic Whipping Cream, Manufactured in Iowa for Kalona Organics, LLC. Kalona IA in 16 FL OZ (UPC 8-81245-12016-2, 8 bottles per case) and 32 FL OZ (UPC 8-81245-12032-2, 6 bottles per case)
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-0057-2022·2021-10-27

    Tropical Trail Mix recalled for glass contamination

    Suntree Snack Foods is recalling Tropical Trail Mix (15 oz bags, UPC 072036735003) because the product may contain glass pieces. Affected lots were distributed across multiple southeastern and mid-Atlantic states.

    Product
    Tropical Trail Mix, 15 oz. , UPC 072036735003. 8 bags/case.
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Drugs)·D-0012-2022·2021-10-27

    Coppertone Pure & Simple Baby Sunscreen Spray Recalled for Benzene Contamination

    Beiersdorf Inc. is recalling Coppertone Pure & Simple Baby 50 Sunscreen Spray nationwide due to the presence of benzene, a chemical contaminant. Consumers should stop using affected products immediately.

    Product
    Coppertone Pure & Simple baby 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02881 7
    Category
    Drug
    Distribution
    Distributed nationwide