The Recall Desk

State

Texas product recalls

72,940 recalls have nationwide distribution and so reach Texas. 12,389 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total
12,389
Critical
1,705
Severe
2,407
Most recent
2026-09-09

Of the 12,389 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 12,389 recalls whose distribution notice names Texas specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4751–4775 of 85329

  • SevereNHTSA·25E076000·2025-11-13

    Eaton Recalls Differentials With Oversized Gear Teeth That May Lock

    Eaton is recalling specific differentials that may lock due to oversized gear teeth, increasing crash risk. Owners should not drive until repaired.

    Product
    POWER TRAIN:DRIVELINE:DIFFERENTIAL UNIT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V784000·2025-11-13

    Fifth wheel trailers recalled over propane lines that can crack and leak

    Grand Design RV is recalling 95 model year 2022-2023 Solitude and 2023 Momentum fifth wheel trailers because loose or missing fasteners can let the refrigerator move and crack the propane line.

    Product
    GRAND DESIGN — GRAND DESIGN MOMENTUM, SOLITUDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26090·2025-11-13

    Power banks and charging stands recalled after overheating fires reported

    About 83,500 Belkin power banks and wireless charging stands are being recalled because the lithium-ion battery can overheat; one US fire and 15 international reports have been received.

    Product
    Portable Power Banks and Wireless Charging Stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26092·2025-11-13

    Home battery systems recalled after overheating smoke and fire reports

    About 10,500 Tesla Powerwall 2 units are being recalled because battery cells can cause the unit to stop working and overheat; 22 overheating reports include five fires.

    Product
    Certain Tesla Powerwall 2 AC Battery Power System
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26086·2025-11-13

    Silicone activity toys recalled after a child gagged and choked on one

    About 117,500 Zippee children's silicone activity toys are being recalled because the spherical string ends can reach the back of the throat; one child gagged, vomited and choked.

    Product
    Zippee Activity Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V783000·2025-11-13

    School buses recalled because the weight rating may be exceeded when full

    International Motors is recalling 142 model year 2023-2027 IC Bus CESB school buses because the bus may exceed its Gross Vehicle Weight Rating when fully occupied with full tanks.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V780000·2025-11-13

    Forest River Bus Recalls Transit Buses With Defective Wheelchair Restraints

    Forest River Bus is recalling 2025-2026 transit buses because wheelchair restraints may fail to lock, increasing injury risk.

    Product
    FOREST RIVER BUS — FOREST RIVER BUS GLAVAL ENTOURAGE, ELDORADO, ELKHART COACH, FOREST RIVER VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V785000·2025-11-13

    Accord Hybrids recalled because a control module reset can cut drive power

    Honda is recalling 256,603 model year 2023-2025 Accord Hybrid vehicles because a software error may reset the integrated control module CPU while driving, causing a loss of drive power.

    Product
    HONDA — HONDA ACCORD HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26088·2025-11-13

    Trek and Electra bicycles recalled because coaster brakes can fail to engage

    About 68,000 Trek and Electra bicycles with coaster brakes, plus replacement rear wheels, are being recalled because the coaster brakes can fail to engage.

    Product
    Trek and Electra-branded Bicycles with Coaster Brakes and Replacement Rear Wheels with Coaster Brakes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26089·2025-11-13

    Coin battery packs recalled for missing child resistant packaging and warnings

    About 32,600 Great Lakes Select button cell and coin battery packs are being recalled because they lack the child-resistant packaging and warning labels required under Reese's Law.

    Product
    Great Lakes Select Button Cell and Coin Batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V779000·2025-11-13

    Forest River Recalls School Buses with Defective Wheelchair Restraints

    Forest River Bus is recalling certain 2025-2027 school buses because wheelchair restraints may fail to lock, increasing injury risk.

    Product
    FOREST RIVER BUS — FOREST RIVER BUS COLLINS SCHOOL BUS, TRANS TECH SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26085·2025-11-13

    Doll sets recalled over button cell batteries children can easily reach

    About 380 Bettina Doll Sets with Magic Light Unicorn are being recalled because the unicorn's battery compartment lets children easily access button cell batteries.

    Product
    Bettina Doll Set with Magic Light Unicorn
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0374-2026·2025-11-12

    Cranial perforators recalled as inadequate weld recall expands to smaller sizes

    Integra LifeSciences is recalling 5,109 CODMAN Disposable Perforators, 9mm, extending an existing 14 mm recall for inadequate welds. The FDA has classified it Class I.

    Product
    CODMAN Disposable Perforator 9mm. Cranial Perforator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0170-2026·2025-11-12

    Pastured large eggs recalled over potential Salmonella contamination in Texas

    Kenz Henz is recalling 16,400 dozen Pastured Grade AA Large Eggs distributed in Texas because the eggs may be contaminated with Salmonella. The FDA has classified the recall as Class I.

    Product
    " Product Name: Pastured Grade AA Large Eggs " Product Description: Egg Carton, 12 eggs per dozen " Pack/Julian Date(s): Julian date 241(Aug 30) to 244 (Sep 2) and 246 (Sep 4) to 247 (Sep 5), Best by Dates 10/11 to 10/14/25 and 10/16 to 10/17.
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Devices)·Z-0427-2026·2025-11-12

    Insulin pumps recalled over false vibration motor failure stopping delivery

    Tandem Diabetes Care is recalling 17,745 Tandem Mobi insulin pumps because a software issue can trigger a false vibration motor failure that halts insulin delivery. The FDA classified it Class I.

    Product
    Tandem Mobi Insulin Pump: Description/Catalog: Tandem insulin pumps are battery-operated infusion pumps capable of both basal and bolus delivery of insulin. The pumps utilize a motor-driven mechanism to deliver insulin from within a disposable cartridge, through an infusion set,
    Category
    Medical Device
    Distribution
    53 states
  • CriticalFDA (Devices)·Z-0373-2026·2025-11-12

    Eleven millimetre cranial perforators recalled over inadequate welds

    Integra LifeSciences is recalling 16,251 CODMAN Disposable Perforators, 11mm, extending an existing 14 mm recall for inadequate welds. The FDA has classified it Class I.

    Product
    CODMAN Disposable Perforator 11mm. Cranial Perforator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V777000·2025-11-12

    Audi SUVs recalled because seat belt buckles may be missing a rivet

    Volkswagen Group of America is recalling certain 2025 Audi Q7, Q8, SQ8 and RS Q8 vehicles because the front seat belt buckles may be missing a rivet that secures the buckle to the stalk.

    Product
    AUDI — AUDI Q8, Q7, RS Q8, SQ8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0421-2026·2025-11-12

    Curved extension catheter trays recalled over header bag seal integrity

    Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays, 12 Fr x 13 cm, over a potential issue with the seal integrity of the header bag packaging.

    Product
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 13 cm;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0162-2026·2025-11-12

    Frozen raw white shrimp recalled over potential Cesium-137 contamination

    AquaStar is recalling 7,200 cases of AquaStar 16/20 Frozen Raw EZ-Peel White Shrimp, sold at WinCo, because the shrimp may be contaminated with Cesium-137.

    Product
    AquaStar 16/20 Frozen Raw EZ-Peel White Shrimp, net wt. 5 lbs. UPC 731149654075. Product was sold at WinCo.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0416-2026·2025-11-12

    Cardiology records system recalled over data saved to the wrong patient

    Spacelabs Healthcare is recalling 142 Sentinel V11 cardiology information systems because patient demographics may default to a previous patient and test data may be saved under another patient's record.

    Product
    Brand Name: Sentinel V11 Product Name: Sentinel V11 Model/Catalog Number: 92810 Software Version: 11.6.0 Product Description: Cardiology Information Management System Component: No The Sentinel Cardiology Information Management System is intended to connect to supported m
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0425-2026·2025-11-12

    Straight extension catheter trays 24 cm recalled over header bag seals

    Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays with straight extensions and IC components, 12 Fr x 24 cm, over header bag seal integrity.

    Product
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 24 cm;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0154-2026·2025-11-12

    Clomipramine 75 mg capsules recalled over nitrosamine above the intake limit

    Zydus Pharmaceuticals is recalling clomiPRAMINE Hydrochloride Capsules USP 75 mg after N-Nitroso Desmethyl-Clomipramine was found above the FDA acceptable intake limit.

    Product
    CLOMIPRAMINE HYDROCHLORIDE — CLOMIPRAMINE HYDROCHLORIDE (CLOMIPRAMINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0426-2026·2025-11-12

    Straight extension catheter trays recalled over header bag seal integrity

    Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays with straight extensions, 12 Fr x 24 cm, over header bag seal integrity.

    Product
    MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Straight Extensions with IC Safety Components: 12 Fr/Ch (4.0 mm) x 24 cm;
    Category
    Medical Device
    Distribution
    Distributed nationwide