The Recall Desk

State

Texas product recalls

73,584 recalls have nationwide distribution and so reach Texas. 12,438 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total
12,438
Critical
1,716
Severe
2,930
Most recent
2026-10-21

Of the 12,438 recalls naming Texas we have scored against our rubric, 1,716 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,930 (24%) are Severe.

These figures cover only the 12,438 recalls whose distribution notice names Texas specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29026–29050 of 86022

  • HighNHTSA·21V267000·2021-04-16

    Pioneer Recalls Prevost H3 and X3 Buses for Fire Risk

    Pioneer Coach Interiors is recalling 2019-2020 Prevost H3 and X3 vehicles because a damaged circuit board increases the risk of a fire.

    Product
    PREVOST — PREVOST H3, X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V266000·2021-04-15

    2022 Thomas Built Buses Minotour Recalled for Electrical Fire Risk

    Daimler Trucks North America is recalling 2022 Thomas Built Buses Minotour vehicles because battery cable terminals may contact a fuse block, causing an electrical short circuit and increasing fire risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V263000·2021-04-15

    Subaru Recalls Crosstrek and Forester for Rear Stabilizer Bolt Defect

    Subaru is recalling 2018-2019 Crosstrek and 2019 Forester vehicles because rear stabilizer bracket bolts may loosen and detach, increasing crash risk.

    Product
    SUBARU — SUBARU CROSSTREK, FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V265000·2021-04-15

    2021 Tiffin Phaeton Motorhomes: Roof Panel Detachment Hazard

    Tiffin is recalling certain 2021 Phaeton motorhomes with roof-mounted awnings. A roof mounted body panel may be improperly attached and could detach, becoming a road hazard and increasing crash risk.

    Product
    TIFFIN — TIFFIN PHAETON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V264000·2021-04-15

    Subaru Recalls Impreza and Crosstrek for Ignition Coil Short Circuit Risk

    Subaru is recalling 2017-2019 Impreza and 2018-2019 Crosstrek vehicles because the engine control module may keep the ignition coil powered after shutdown, causing a short circuit and potential stall.

    Product
    SUBARU — SUBARU CROSSTREK, IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1332-2021·2021-04-14

    Tenacore Alaris Infusion Pump Bezel Recall for Cracking Risk

    Tenacore LLC is recalling Alaris Infusion Pump 8100 bezels because they may crack or separate, potentially causing infusion errors.

    Product
    Alaris Infusion Pump 8100 Bezel (plastic piece only), Part: TIPA-8100-4410
    Category
    Medical Device
    Distribution
    16 states
  • SevereFDA (Devices)·Z-1331-2021·2021-04-14

    Tenacore Recalls Alaris Infusion Pump Modules with Impacted Bezel Repair Parts

    Tenacore LLC is recalling 474 Alaris Infusion Pump Modules, Model 8100, serviced with non-original bezel repair parts. The parts may crack or separate, potentially causing infusion errors.

    Product
    Alaris Infusion Pump Module, Model 8100, serviced/repaired by Tenacor with an impacted bezel repair part
    Category
    Medical Device
    Distribution
    16 states
  • SevereFDA (Food)·F-0383-2021·2021-04-14

    Bobo's Maple Pecan Oat Bars Recalled for Peanut Complaints

    Simply Delicious Inc. is recalling Bobo's Maple Pecan Oat Bars due to consumer complaints regarding the presence of peanuts.

    Product
    Bobo's Maple Pecan Oat Bars, 3 oz., UPC 8 2926200021 0, Best By 7/30/21 or 7/31/21.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0326-2021·2021-04-14

    Alembic Pharmaceuticals Recalls Telmisartan Tablets Due to Labeling Error

    Alembic Pharmaceuticals is recalling 12,288 bottles of Telmisartan 20 mg tablets due to a label mixup. The product was distributed nationwide in the United States.

    Product
    TELMISARTAN — TELMISARTAN (TELMISARTAN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1343-2021·2021-04-14

    Fenwal Recalls Amicus MNC Apheresis Kits Due to Centrifuge Pack Leaks

    Fenwal Inc is recalling specific lots of Amicus MNC Apheresis Kits because centrifuge packs may leak blood during therapeutic procedures.

    Product
    Amicus MNC Apheresis Kit - Double Needle - Product Usage: intended for use in the collection of blood components and mononuclear cells.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1378-2021·2021-04-14

    Becton Dickinson Recalls Martin-Lewis Agar Due to Fungal Growth

    Becton Dickinson is recalling Martin-Lewis Agar plates because they show heavy fungal growth, which may delay the diagnosis of Neisseria infections.

    Product
    BD BBL Martin-Lewis Agar 20 Ea - Product Usage: use for the isolation of pathogenic Neisseria from specimens containing mixed flora of bacteria and fungi. Catalog Number: 221557
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1374-2021·2021-04-14

    Arrow OnControl Bone Lesion Biopsy System Recalled for Insertion Defect

    Arrow International is recalling OnControl Bone Lesion Biopsy Systems because the ejector rod may not insert properly, preventing sample collection.

    Product
    Arrow OnControl Bone Lesion Biopsy System Tray-11 ga 10 cm Access/13 ga 14 cm Biopsy, Product Code: 9464-VC-006 (US) Product Code: 9464-EU-001 (sold in European Regions only) - Product Usage: intended for bone biopsy of the vertebral body and bone lesions.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21111·2021-04-14

    Target Recalls Cat & Jack Baby Rompers Due to Choking Hazard

    Target is recalling Cat & Jack Baby Heart Ears Rompers because heart-shaped graphics on the knees can detach, posing a choking hazard to children.

    Product
    Cat & Jack Baby Heart Ears Rompers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0389-2021·2021-04-14

    Trident Seafoods Pacific Salmon Burgers Recalled for Metal Fragment

    Trident Seafoods is recalling frozen Pacific Salmon Burgers sold at Costco due to a metal fragment found in the product.

    Product
    Trident Seafoods Pacific Salmon Burgers (# 414469), frozen. Costco item #502497. Each retail bag contains of 12/4oz. pieces. Retail bag net wt. 48 oz (3 lb or 1.36 kg). Retail bag UPC 0 28029 14469 7. Each Master case contains of 12/3 lbs. packages. The MASTER CASE label is…
    Category
    Food
    Distribution
    3 states
  • HighCPSC·21112·2021-04-14

    Playgro Recalls Clip Clop Infant Activity Rattles Due to Choking Hazard

    Playgro is recalling Clip Clop infant activity rattle toys because the abacus ring can dislodge and release small beads, posing a choking hazard to small children.

    Product
    Clip Clop Infant Activity Rattles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1366-2021·2021-04-14

    Sharp Medical Reactor and Sleeve Recalled for Sterile Barrier Defects

    Sharp Medical Products is recalling 129 units of Reactor and Sleeve REF 100-36-01 due to holes, punctures, or deep creases in the sterile barrier.

    Product
    SHARP MEDICAL PRODUCTS, LLC Reactor and Sleeve REF 100-36-01 Size: Adult
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-1379-2021·2021-04-14

    Howmedica Recalls Specialty Triathlon TS Trial Cutting Guides Due to Fracture Risk

    Howmedica Osteonics Corp. is recalling Specialty Triathlon TS Trial Cutting Guides because the posterior condyle may fracture during transport or surgery.

    Product
    Trial Cutting Guide for Triathlon Total Knee System, Triathlon PKR System, Restoris MCK Knee System, prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer/metal/polymer. Catalog Number: I-K3834CG00 Specialty Triathlon TS Trial Cutting Guide Set…
    Category
    Medical Device
    Distribution
    7 states
  • HighFDA (Devices)·Z-1344-2021·2021-04-14

    Fenwal Recalls Amicus Exchange Kits Due to Centrifuge Pack Leaks

    Fenwal Inc is recalling 2,466 Amicus Exchange Kits because centrifuge packs may leak blood during therapeutic procedures.

    Product
    Amicus Exchange Kit - Product Usage: intended for use in the collection of blood components and mononuclear cells.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1372-2021·2021-04-14

    Beckman Coulter MicroScan WalkAway-40 Plus Reconditioned Instruments Recalled

    Beckman Coulter is recalling six reconditioned MicroScan WalkAway-40 Plus instruments due to a shortened reagent draw straw that may cause reagent dispensing failures and organism misidentification.

    Product
    MicroScan WalkAway-40 plus Reconditioned Instrument
    Category
    Medical Device
    Distribution
    15 states
  • HighCPSC·21109·2021-04-14

    Battat Recalls Firefly Frank Infant Teethers Due to Choking Hazard

    Battat is recalling B. toys Firefly Frank infant teethers sold at Target because plastic wings can detach, posing a choking hazard to young children.

    Product
    B. toys Firefly Frank Infant Teethers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1376-2021·2021-04-14

    ROi CPS Recalls Regard Custom Cardiovascular Procedure Kits

    ROi CPS LLC is recalling 16 Regard custom cardiovascular procedure kits because drape slits may breach the sterile barrier.

    Product
    Regard, Item Number 830067009, custom cardiovascular procedure kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1345-2021·2021-04-14

    Fenwal Recalls Amicus Exchange Kits Due to Centrifuge Pack Leaks

    Fenwal Inc is recalling 24 units of Amicus Exchange Kits because centrifuge packs may leak blood during therapeutic procedures.

    Product
    Amicus Exchange Kit Therapeutics - Product Usage: intended for use in the collection of blood components and mononuclear cells.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1346-2021·2021-04-14

    Siemens Ysio X.pree Digital X-Ray System Recalled for Image Mismatch

    Siemens is recalling 12 Ysio X.pree digital X-ray systems because a software issue may display a previous patient's image during recovery, potentially impacting diagnosis.

    Product
    Ysio X.pree, Model Number: 11107464 - Product Usage: A Digital X-Ray System generate Xray images from the whole body including the skull, chest, abdomen, and extremities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1370-2021·2021-04-14

    Beckman Coulter Recalls MicroScan WalkAway-40 plus Instruments

    Beckman Coulter is recalling 16 MicroScan WalkAway-40 plus instruments because a shortened reagent straw may cause reagent dispensing failures, leading to organism misidentification or quality control failures.

    Product
    MicroScan WalkAway-40 plus Instrument
    Category
    Medical Device
    Distribution
    15 states
  • HighCPSC·21110·2021-04-14

    Audio-Technica Recalls Wireless Headphone Charging Cases Due to Fire Hazard

    Audio-Technica is recalling charging cases for ATH-CK3TW wireless headphones because they can overheat and pose a fire hazard. No injuries have been reported.

    Product
    Charging Cases Sold with Audio-Technica Wireless Headphones, Model ATH-CK3TW
    Category
    Consumer Product
    Distribution
    Distributed nationwide