The Recall Desk

State

Texas product recalls

72,992 recalls have nationwide distribution and so reach Texas. 12,390 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total
12,390
Critical
1,705
Severe
2,407
Most recent
2026-09-16

Of the 12,390 recalls naming Texas we have scored against our rubric, 1,705 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,407 (19%) are Severe.

These figures cover only the 12,390 recalls whose distribution notice names Texas specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8126–8150 of 85382

  • SevereCPSC·25169·2025-03-13

    Sublue Mix Underwater Scooters Recalled for Lithium-Ion Battery Fire Hazard

    Sublue is recalling about 40,370 Mix underwater scooters and batteries with lithium-ion cells that can overheat and catch fire. Reports include 8 fires, 1 injury, and significant property damage.

    Product
    Sublue Mix underwater scooters and replacement batteries (black batteries only)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25182·2025-03-13

    Onasti Toddler Tower Stools Recalled for Fall and Injury Risk

    Onasti Toddler Tower Stools sold on Amazon can collapse or tip over while in use, posing fall and injury risks. Recalls follow four reports of incidents, including injuries.

    Product
    Onasti Toddler Tower Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V156000·2025-03-13

    GM Recalls BrightDrop Zevo Vehicles for Steering Shaft Defect

    General Motors is recalling 2023-2024 BrightDrop Zevo 600 and 2024 Zevo 400 vehicles because a damaged steering shaft may cause the steering to lock up, increasing crash risk.

    Product
    BRIGHTDROP — BRIGHTDROP ZEVO 400, ZEVO 600
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E019000·2025-03-13

    Zoox Robotaxi Recall for Unexpected Hard Braking Software Defect

    Zoox is recalling 2023-2024 Robotaxis because a software defect may cause unexpected hard braking in certain driving scenarios, increasing crash risk.

    Product
    ZOOX — ZOOX ZOOX ROBOTAXI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25178·2025-03-13

    Retractable Safety Gates Recalled for Risk of Child Entrapment

    HabiLife Direct retractable safety gates (model SG021) are recalled due to an entrapment hazard where children's torsos can fit through gaps between the gate and floor. About 880 units sold on Amazon from September 2024 through January 2025.

    Product
    Retractable Safety Gates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25180·2025-03-13

    Chews Life Recalls Silicone Rosary and Decade Teethers for Choking Hazard

    About 5,700 Chews Life Silicone Rosary and Decade teethers are being recalled because the safety snap clasp can detach, posing a choking hazard to infants. No injuries have been reported.

    Product
    Silicone Rosary and Decade teethers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25181·2025-03-13

    Climbing Harness Recalled for Potential Degradation and Fall Risk

    Black Diamond Equipment recalls BD Vision climbing harnesses due to potential degradation that could cause harness failure and falls. No injuries have been reported to date.

    Product
    BD Vision Climbing Harness
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25179·2025-03-13

    Meijer Recalls Konwin Desktop Heaters Due to Fire and Burn Hazards

    Meijer is recalling about 6,050 Konwin desktop heaters because the fan can fail to turn on, causing the unit to overheat and ignite. The company received eight reports of fans burning and melting, but no injuries have been reported.

    Product
    Konwin Desktop Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25177·2025-03-13

    BMC recalls Kaius 01 bicycles and framesets for fork separation hazard

    BMC recalled about 1,300 Kaius 01 bicycles because the fork steerer tube can crack and separate during use, posing a fall hazard. No injuries reported; consumers should stop using them and contact dealers for free fork replacement.

    Product
    BMC-branded Kaius 01 bicycles and framesets
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25183·2025-03-13

    Gerolsteiner Sparkling Water Bottles Recalled Due to Laceration Hazard

    Gerolsteiner 750ml sparkling water bottles sold at Trader Joe's locations are being recalled because the glass bottles can crack, creating a laceration hazard. No injuries have been reported.

    Product
    Gerolsteiner 750ml Sparkling Water Bottles
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1257-2025·2025-03-12

    Insulin pump recall: Medtronic Paradigm models malfunction during airplane flight

    Medtronic MiniMed's Paradigm insulin pumps can malfunction during airplane flight due to air pressure changes, potentially causing dangerously high or low blood sugar levels that could be fatal.

    Product
    Paradigm insulin pump, REF: MMT-754
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1244-2025·2025-03-12

    Rotarex Atherectomy Catheter Recalled for Helix Fracture Risk

    Bard is recalling Rotarex Atherectomy System catheters due to potential helix fracture or breakage that could cause vessel injury and severe bleeding. Updated instructions are being distributed to clarify procedural steps to reduce this risk.

    Product
    Rotarex Atherectomy System and Instructions for Use, BD SET Rotarex: S 6 F x 110 cm, REF: 80236; S 6 F x 135 cm, REF: 80237; S 8 F x 85 cm, REF: 80238; S 8 F x 110 cm, REF: 80239
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0588-2025·2025-03-12

    Watermelon and Cucumber Products Recalled for Potential Salmonella Contamination

    JFE Franchising is recalling watermelon and cucumber products with Tajin seasoning due to potential Salmonella contamination. Affected packages were distributed in TX, LA, WY, and AZ with sell-by dates from October 12 through December 5, 2024.

    Product
    Mixed Melon, Cucumber & Tajin 18 oz Watermelon & Cucumber w/ Tajin 18 oz packed in clamshells
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1245-2025·2025-03-12

    Medtronic Pipeline Vantage Embolization Device Recall for Structural Deformation Risk

    Medtronic is recalling approximately 18,245 unused Pipeline Vantage embolization devices due to incomplete wall apposition and braid deformation that may lead to thrombosis and serious adverse events.

    Product
    Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-027-350-12, PED3-027-350-14, PED3-027-350-16, PED3-027-350-20, PED3-027-350-25, PED3-027-400-12, PED3-027-400-14, PED3-027-400-16, PED3-027-400-18, PED3-027-400-20, PED3-027-400-25, PED3-027-400-30,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V154000·2025-03-12

    BMW X3 rear brake hoses may leak and disable rear braking

    BMW is recalling certain 2025 X3 30 xDrive and X3 M50 xDrive vehicles because the rear brake hoses may leak, causing a loss of rear brake function, ABS and stability control.

    Product
    BMW — BMW X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0606-2025·2025-03-12

    Amazon Fresh Jumbo Sugar Cookies recalled for undeclared egg allergen

    Amazon Retail LLC is recalling Amazon Fresh Jumbo Sugar Cookies nationwide due to undeclared egg, a major allergen. Consumers with egg allergies should not consume the affected cookies.

    Product
    ASIN B084PZ7K98, Amazon Fresh Jumbo Sugar Cookie, 27 oz (12 count), product is baked and packaged in flexible plastic bag. 4-day shelf life. UPC 465712007998. ASIN B084PX9V31, Amazon Fresh Jumbo Sugar Cookie, 2.3 oz (1 count), product is baked and sold from open pastry tray in s
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0586-2025·2025-03-12

    Cucumber Products Recalled Due to Potential Salmonella Contamination

    JFE Franchising Inc. is recalling packaged cucumber products distributed in TX, LA, WY, and AZ due to potential Salmonella contamination. Consumers should not consume these products.

    Product
    Cucumber, Lime & Tajin 19 oz Cucumber with Ranch 9 oz Cucumber Bowl with Ranch 15 oz Cucumber Slices with Tajin 15 oz packed in clamshells
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1205-2025·2025-03-12

    FDA Recalls VARIPULSE Bi-Directional Ablation Catheter Due to Neurovascular Events

    Biosense Webster is recalling VARIPULSE Bi-Directional Ablation Catheters (REF D141201) due to an observed trend of neurovascular events. The FDA issued a Class I recall affecting approximately 497 units distributed worldwide.

    Product
    VARIPULSE Bi-Directional Ablation Catheter REF D141201. The Field Catheter is indicated for use in catheter based cardiac electrophysiological mapping (stimulating and recording) and, when used for TRUPULSE Generator, for the treatment of drug refractory recurrent symptomat
    Category
    Medical Device
    Distribution
    10 states
  • SevereNHTSA·25V046000·2025-03-12

    Freightliner Recalls eCascadia and eM2 Trucks for Power Loss Risk

    Daimler Trucks North America is recalling 2020-2026 Freightliner eCascadia and eM2 trucks because a faulty power module may cause a loss of drive power, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER E-CASCADIA, EM2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V152000·2025-03-12

    Shyft Recalls 2025 Utilimaster Upfit Vehicles for Loose Seat Bolts

    Shyft Group is recalling 2025 Utilimaster Upfit vehicles because passenger jump seat mounting bolts may not be properly tightened, increasing injury risk in a crash.

    Product
    UTILIMASTER — UTILIMASTER UPFIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0587-2025·2025-03-12

    Vegetable trays and bowls recalled for potential Salmonella contamination

    JFE FRANCHISING INC is recalling vegetable bowls and trays sold in TX, LA, WY, and AZ due to potential Salmonella contamination. Consumers should not consume these products.

    Product
    Vegetable Bowl 13 oz Small Vegetable Tray 19.5 oz Vegetable Bowl 26 oz Large Vegetable Tray 42 oz packed in clamshells
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1253-2025·2025-03-12

    Baxter Sigma Spectrum Infusion System Recalled for Missing Mounting Screws

    Baxter Healthcare is recalling 66 units of Sigma Spectrum Infusion System (V6) due to potential missing motor mounting screws that may have occurred during servicing. Missing screws could affect the device's operation.

    Product
    Baxter Sigma Spectrum Infusion System (V6 Platform), Product Code 35700BAX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0607-2025·2025-03-12

    Frozen Sugar Cookie Dough Recalled for Undeclared Egg Allergen

    Amazon Fresh Bake at Home Jumbo Sugar Cookie dough is being recalled due to undeclared egg. Consumers with egg allergies should not consume this product.

    Product
    ASIN B0CY2RDW5T, Amazon Fresh brand, Bake at Home Jumbo Sugar Cookie 30oz, product is frozen dough, and packaged in flexible plastic bag. UPC 446472006995.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1254-2025·2025-03-12

    Baxter Spectrum IQ Infusion System may have missing motor mounting screws

    Baxter Spectrum IQ Infusion Systems may lack motor mounting screws due to a servicing defect. The FDA Class I recall affects 323 units distributed nationwide.

    Product
    Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009
    Category
    Medical Device
    Distribution
    Distributed nationwide