The Recall Desk

State

Texas product recalls

73,106 recalls have nationwide distribution and so reach Texas. 12,428 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total
12,428
Critical
1,720
Severe
2,422
Most recent
2026-10-02

Of the 12,428 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 2,422 (19%) are Severe.

These figures cover only the 12,428 recalls whose distribution notice names Texas specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12851–12875 of 85534

  • HighFDA (Devices)·Z-1741-2024·2024-05-08

    RayStation 7.0.0.19 radiation therapy planning software recalled for dose calculation error

    RayStation 7.0.0.19, a radiation therapy treatment planning system, is being recalled due to potential source-to-surface distance (SSD) calculation errors that could affect radiation dose accuracy. The recall affects 14 units distributed worldwide.

    Product
    RayStation 7.0.0.19. Radiation Therapy Treatment Planning System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1748-2024·2024-05-08

    Radiation Therapy Planning System May Calculate Skin Surface Distance Incorrectly

    RayStation radiation therapy planning software versions 11.0.0.951, 11.0.1.29, 11.0.3.116, and 11.0.4.15 may calculate skin surface distance (SSD) values incorrectly, potentially affecting dose calculations. Affected software has been distributed worldwide.

    Product
    RayStation 11.0.0.951, 11.0.1.29, 11.0.3.116 & 11.0.4.15. Radiation Therapy Treatment Planning System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1717-2024·2024-05-08

    Zimmer Periarticular Locking Plate recalled for improper screw mating defect

    Zimmer, Inc. is recalling the ZPLP Distal Lateral Fibular Plate due to a thread form defect that may prevent locking screws from properly mating with the plate, potentially causing surgical delays or loss of fixation.

    Product
    ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 8 Holes, 132 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 47-2357-018-08
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1709-2024·2024-05-08

    Zimmer Distal Lateral Fibular Plate may fail to lock screws securely

    Zimmer's Distal Lateral Fibular Plate has threading defects that may prevent screws from locking properly. The defect could go unnoticed during surgery and cause loss of fixation.

    Product
    ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 4 Holes, 80 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 47-2357-017-04
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1742-2024·2024-05-08

    Radiation therapy planning system may report overly high skin surface doses

    RayStation versions 8.0.0.61 and 8.0.1.10 are subject to a Class II FDA recall due to a potential for calculated skin surface doses to be reported as too high. Healthcare facilities using these versions should contact the manufacturer for guidance and a corrective update.

    Product
    RayStation 8.0.0.61, 8.0.1.10. Radiation Therapy Treatment Planning System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1746-2024·2024-05-08

    RayStation Radiation Therapy Planning Software Recalled for Calculation Error

    RayStation radiation therapy planning software versions 10.0.0.1154, 10.0.1.52, and 10.0.2.10 have been recalled due to a potential calculation parameter issue that could affect treatment planning. The FDA classified this as a Class II recall affecting 213 units worldwide.

    Product
    RayStation 10.0.0.1154, 10.0.1.52 & 10.0.2.10. Radiation Therapy Treatment Planning System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1207-2024·2024-05-08

    Longreen Cordyceps Coffee recalled for undeclared soy and coconut allergens

    BF Suma Pharmaceuticals is recalling Longreen Corporation 4 in1 Cordyceps Coffee due to undeclared soy lecithin and coconut oil allergens. Affected products were distributed to California, Texas, Canada, and Guatemala.

    Product
    Longreen Corporation 4 in1 Cordyceps Coffee, 18.2 grams/sachet, 10 sachets/box
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1705-2024·2024-05-08

    Zirconium oxide dental blocks recalled due to cracking and fracture risk

    IVOCLAR VIVADENT is recalling IPS e.max ZirCAD zirconium oxide blocks nationwide because they may develop cracks after sintering that could cause dental restorations to fracture in patients' mouths.

    Product
    IPS e.max ZirCAD CER/in. Prime A2 C17/5 -A zirconium oxide block for the fabrication of fixed, full-contour restorations in anterior and posterior teeth. Article Number: 758438
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1206-2024·2024-05-08

    Longreen Corporation Reishi Coffee recalled for undeclared soy and coconut allergens

    BF Suma Pharmaceuticals is recalling Longreen Corporation 4 in1 Reishi Coffee because soy lecithin and coconut oil were not declared on the label. Consumers with soy or coconut allergies could have allergic reactions.

    Product
    Longreen Corporation 4 in1 Reishi Coffee, 18.2 grams/sachet, 10 sachets/box
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1756-2024·2024-05-08

    Philips Spectral CT Oncology Imaging System Recall: Laser Reflection Hazard

    Philips recalls 12 units of its Spectral CT Oncology Essentials system because a marking laser could reflect off the gantry cover, potentially causing misdiagnosis and incorrect patient treatment.

    Product
    The Oncology Essentials Package of the Spectral CT imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1704-2024·2024-05-08

    Zirconium oxide dental blocks recalled due to cracking risk

    IVOCLAR VIVADENT AG is recalling 7,445 units of IPS e.max ZirCAD CER/in. Prime zirconium oxide blocks because they may crack during sintering, potentially causing dental restorations to fracture in patients' mouths.

    Product
    IPS e.max ZirCAD CER/in. Prime A1 C17/5 - A zirconium oxide block for the fabrication of fixed, full-contour restorations in anterior and posterior teeth. Article Number: 758437
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1753-2024·2024-05-08

    Hip Cup Removal Instrument Recalled Due to Wrong Blade Assembly

    Innomed is recalling the Cup Removal Starter Instrument due to a manufacturing error where the finisher blade was affixed instead of the starter blade. The wrong blade could compromise surgical performance during hip replacement procedures.

    Product
    INNOMED CUP REMOVAL STARTER INSTRUMENT, REF 520054, Hip cutter blade cup
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Drugs)·D-0478-2024·2024-05-08

    Injectable epinephrine-lidocaine recalled for failing potency specification

    Imprimis NJOF, LLC is recalling epinephrine-lidocaine injectables nationwide because they failed to meet potency specifications. Patients should contact their healthcare provider regarding affected lots.

    Product
    Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL Preservative-Free, 1 mL Single-Use vials, Rx only, Imprimis NJOF, LLC 1705 Route 46 West, Unit 6B, Ledgewood, NJ, 07852, NDC 71384-640-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0481-2024·2024-05-08

    Prescription Valacyclovir Tablets Recalled Due to Missing Imprint

    Viatris Inc is recalling 143,230 bottles of Valacyclovir Hydrochloride 500 mg tablets due to missing imprints on some tablets. The recall is nationwide and affects two lot numbers expiring in June 2024 and May 2025.

    Product
    VALACYCLOVIR HYDROCHLORIDE — VALACYCLOVIR HYDROCHLORIDE (VALACYCLOVIR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0480-2024·2024-05-08

    Fentanyl Injection Bags Recalled Due to Incorrect Barcode Labels

    Hikma Injectables USA Inc. has recalled 1,895 bags of Fentanyl 1000mcg/100mL injection (lot CH0324001) due to incorrect barcodes on the product labeling.

    Product
    Fentanyl 1000mcg/100mL (10mcg/mL) in 0.9% Sodium Chloride Injection, packaged in 100mL bags, Rx only, Compounded by: Hikma Injectables USA Inc. 2 Esterbrook Lane, Cherry Hill, NJ 08003, Distributed by: Hikma Injectables USA Inc. 36 Stults Road, Dayton, NJ 08810, NDC 63037-100-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·24V318000·2024-05-07

    Winnebago motorhomes recalled for airbag system wiring damage

    Winnebago motorhomes are being recalled due to airbag system wiring that can be trapped in the seat mechanism when seats are adjusted. Damaged wires could prevent the airbags from deploying in a crash.

    Product
    WINNEBAGO — WINNEBAGO ADVENTURE WAGON, VITA, REVEL, PORTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V264000·2024-05-06

    Autocar Recalls 2020-2024 Legend Vehicles Due to Wiring Fire Risk

    Autocar is recalling 2020-2024 Legend vehicles because the wiring harness may route fusible links too closely to other components, increasing the risk of a fire during a short circuit.

    Product
    AUTOCAR — AUTOCAR LEGEND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V317000·2024-05-06

    Coach and Equipment Recalls 2024 Phoenix Shuttle Buses for Seat Defect

    Coach and Equipment is recalling 2024 Phoenix shuttle buses because the seat recliner mechanism may not engage, increasing injury risk during a crash.

    Product
    COACH AND EQUIPMENT — COACH AND EQUIPMENT PHOENIX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V316000·2024-05-06

    2024 Mercedes-Benz eSprinter Brake Control Software Defect Recall

    Daimler Vans USA is recalling certain 2024 Mercedes-Benz eSprinter vehicles due to a software error in the electronic stability program that may extend braking distance and increase crash risk. Dealers will provide a free software update.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ ESPRINTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E035000·2024-05-03

    Autoliv Recalls Roof Rail Air Bag Inflators Due to Rupture Risk

    Autoliv is recalling specific roof rail air bag inflators that may fail at the weld joint, potentially causing gas leaks or ruptures that increase injury risk.

    Product
    AIR BAGS:SIDE/WINDOW recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V313000·2024-05-03

    Forest River Recalls Rockport Work Trucks Due to Liftgate Defect

    Forest River is recalling certain Rockport Work Trucks because the rear liftgate may fall if a U-bolt is missing, increasing injury risk.

    Product
    FOREST RIVER — FOREST RIVER ROCKPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V314000·2024-05-03

    Airstream Atlas Motorhome Generator Recalled for Missing Heat Shield

    Certain 2023-2024 Airstream Atlas motorhomes may lack a heat shield on the generator, exposing subflooring to excessive heat. This defect increases the risk of fire and injury.

    Product
    AIRSTREAM — AIRSTREAM ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·24V315000·2024-05-03

    Heartland Recalls 2024 Eddie Bauer Travel Trailers for Incorrect Tire Placards

    Heartland is recalling 2024 Eddie Bauer travel trailers because tire placards list the wrong tire size. This labeling error could lead to incorrect tire installation and increased crash risk.

    Product
    HEARTLAND — HEARTLAND EDDIE BAUER
    Category
    Vehicle
    Distribution
    Distributed nationwide