The Recall Desk

State

Texas product recalls

73,363 recalls have nationwide distribution and so reach Texas. 12,434 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total
12,434
Critical
1,720
Severe
2,425
Most recent
2026-10-07

Of the 12,434 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 2,425 (20%) are Severe.

These figures cover only the 12,434 recalls whose distribution notice names Texas specifically. The 73,363 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18426–18450 of 85797

  • ModerateCPSC·23757·2023-05-18

    Shimano PRO Vibe Alloy Bicycle Stems Recalled for Crack and Injury Risk

    Shimano is recalling about 400 PRO Vibe Alloy stems for road bicycles because the stems can crack and break during use, causing loss of control and crash risk. Two reports of cracking have been received in the U.S., but no injuries have been reported.

    Product
    Shimano PRO Vibe Alloy stems for road bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23758·2023-05-18

    Cole & Mason Pepper Mills Recalled for Metal Shard Laceration Hazard

    DKB Household is recalling Cole & Mason 505WEG Pepper Mills due to a metal grinding mechanism that sheds metal shards during initial use, posing a laceration risk. No injuries have been reported.

    Product
    Cole & Mason 505WEG Pepper Mills Item Number H50501PWE
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1427-2023·2023-05-17

    Blue Rhino G2 Tracheostomy Introducer Sets Recalled for Unsecure Connections

    Cook Incorporated is recalling Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Sets due to unsecure connections with 15mm caps and circuit components that may disconnect during medical procedures.

    Product
    Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set, Reference Part Numbers C-PTIS-100-HC-G-EU-FLEX7.5 (G57695), C-PTIS-100-HC-G-EU-FLEX8.5 (G57696), C-PTIS-100-HC-G-NA-FLEX7.5 (G57691), C-PTIS-100-HC-G-NA-FLEX8.5 (G57692)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0871-2023·2023-05-17

    Takuma Herb Salt Peanuts Recalled for Undeclared Fish Allergen

    Daiso California Warehouse is recalling Takuma food herb salt peanuts because the product contains fish (Bonito, Sardines, Tuna) but does not list it on the label. Consumers with fish allergies could unknowingly consume the product.

    Product
    Takuma food herb salt peanut 80g UPC: 4962679652767
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0876-2023·2023-05-17

    FDA Recalls Kimura Burdock Salt for Undeclared Fish Allergen

    Daiso California Warehouse is recalling Kimura burdock salt because it contains fish (sardines, bonito, tuna) not listed on the label. People with fish allergies may have a serious allergic reaction.

    Product
    Kimura burdock salt 40g UPC: 4972304293524
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0841-2023·2023-05-17

    Vitamin B Capsules Recalled for Undeclared Milk Allergen

    EuroMedica and Terry Naturally vitamin B complex capsules are being recalled nationwide due to undeclared milk allergen. Consumers with milk allergies should not use these products.

    Product
    Multiple Vitamin B Capsules, 60 Capsules, Biologically Active Forms of Vitamin B12, Folate, B6. Packaged in bottles under the following brands: 1. EuroMedica Active B Complex, Product #68006, UPC 3 67703 68006 0. Manufactured by a cGMP compliant facility exclusively for…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0567-2023·2023-05-17

    Atovaquone Oral Suspension Recalled for Bacillus cereus Contamination

    Camber Pharmaceuticals is recalling Atovaquone Oral Suspension due to contamination by Bacillus cereus bacteria. The contamination was discovered during testing of repackaged medication.

    Product
    ATOVAQUONE — ATOVAQUONE (ATOVAQUONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1428-2023·2023-05-17

    Cook Blue Rhino G2 Tracheostomy Introducer Trays Recalled for Connection Defect

    Cook Incorporated is recalling Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Trays because the device connectors are not making secure connections with 15mm caps and other circuit components, resulting in unsecure connections.

    Product
    Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray, Reference Part Numbers C-PTISYJ-100-HC-G-EU-FLEX8.5 (G57725), C-PTISYJ-100-HC-G-NA-FLEX7.5 (G57720), C-PTISYJ-100-HC-G-NA-FLEX8.5 (G57721), C-PTISY-100-HC-G-NA-FLEX8.5 (G57717), C-PTISY-100-HC-G-NA-FLEX7.5 (G57716)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V349000·2023-05-17

    Foretravel Recalls 2022-2024 Motorhomes Due to Software Error

    Foretravel is recalling 2022-2024 Realm, FS450, and Realm Presidential motorhomes because a software error may cause loss of drive power or disable safety systems.

    Product
    FORETRAVEL — FORETRAVEL REALM, FS450, REALM PRESIDENTIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1564-2023·2023-05-17

    Bard Mission Biopsy Instrument Kit cannula and needle incompatibility

    Bard Mission Disposable Biopsy Instrument Kit has an incompatibility defect where the cannula is oversized relative to the needle, preventing proper insertion and tissue access. This could cause procedure delays and insufficient tissue collection.

    Product
    Bard Mission Disposable Core Biopsy Instrument Kit: REF: 2010MSK, 20G x 10CM; REF: 2016MSK, 20G x 16CM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1577-2023·2023-05-17

    STA Compact Max analyzer firmware bug causes inaccurate test results

    A firmware bug in Diagnostica Stago's STA Compact Max analyzer causes intermittent shortened coagulation times and frequent technical errors that produce inaccurate lab test results. Five units were distributed to clinical laboratories nationwide.

    Product
    STA Compact Max fully automatic clinical analyzer, Reference Numbers 58602 and 58612
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0830-2023·2023-05-17

    Ziyad Cinnamon Powder Recalled for Elevated Lead Levels

    ZB Importing LLC is recalling Ziyad cinnamon powder (4.5 oz jars) from lot 21321G2 due to elevated lead levels. The recall affects 3,456 units distributed across multiple U.S. states and territories.

    Product
    Ziyad cinnamon powder, retail 4.5oz plastic jar with shaker cap UPC 074265007432, 12 retail jars per wholesale case
    Category
    Food
    Distribution
    35 states
  • HighFDA (Devices)·Z-1575-2023·2023-05-17

    STA R Max Analyzer Firmware Bug Produces Inaccurate Coagulation Test Results

    Diagnostica Stago is recalling the STA R Max fully automatic clinical analyzer due to a firmware bug that causes intermittent shortened coagulation times and increased technical errors, potentially producing inaccurate blood clotting test results.

    Product
    STA R Max fully automatic clinical instrument designed to perform tests on human plasmas, Reference Numbers 59013 and 59026
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1572-2023·2023-05-17

    APLS IgM Diagnostic Reagent Packs Recalled Due to Incorrect Conjugate

    Bio-Rad Laboratories is recalling 932 BioPlex 2200 APLS IgM Reagent Packs (Lot 301538) nationwide because they were packaged with incorrect conjugate. This could result in false-positive and false-negative test results.

    Product
    BioPlex 2200 REF 665-2050, APLS IgM Pack, APLS IgM Reagent Pack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0860-2023·2023-05-17

    Ajikal Age Ichiban Snack Recalled for Undeclared Coconut Allergen

    Ajikal Age Ichiban 97g snacks are being recalled due to undeclared coconut, a tree nut allergen that can cause allergic reactions. The affected product was distributed across multiple US states and Canada.

    Product
    Ajikal Age Ichiban 97g UPC: 4510656600906
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1579-2023·2023-05-17

    BD Pyxis MedStation ES software failure causes patient data loss

    BD Pyxis automated dispensing cabinet software versions 1.7.0 through 1.7.4 experience download failures causing partial loss of patient information and transaction data. This may result in dispensing incorrect medication doses, allergenic medications, or discontinued medications.

    Product
    BD Pyxis MedStation ES (Med ES Main), REF: 323; BD Pyxis MedStation ES (Med ES Main Tower), REF: 352; BD Pyxis Anesthesia Station ES, REF: 327; BD Pyxis CII Safe ES Tower Main, REF: 1116-00; BD Pyxis CII Safe ES, Desktop PC, W-LESS SCNR, BIO, REF: 107-255-01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0874-2023·2023-05-17

    Kajitani Food Congeri Crispy recalled due to undeclared coconut allergen

    Kajitani Food Congeri Crispy crackers (104g, UPC 4901332108661) contain coconut but do not list it in the ingredients or allergen statement. Consumers with coconut allergies may be at risk; approximately 2,199 units were distributed to retail locations across multiple US states and Canada.

    Product
    Kajitani Food Congeri Crispy 104g UPC: 4901332108661
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1576-2023·2023-05-17

    STA Compact Analyzer Firmware Bug Causes Inaccurate Test Results

    Diagnostica Stago is recalling STA Compact Analyzers due to a firmware bug causing intermittent shortened coagulation times and increased technical errors. No illnesses or injuries have been reported.

    Product
    STA Compact Automated Multi-Parametric Analyzer, Reference Numbers 58602 and 58612
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0873-2023·2023-05-17

    Kanro Non-Sugar Tea House Recalled for Undeclared Coconut Allergen

    Kanro Non-Sugar Tea House 40g has been recalled because coconut allergen is not listed in the product ingredients. Consumers with coconut allergies should not consume this product.

    Product
    Kanro Non-Sugar Tea House 40g UPC: 4901351013144
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0872-2023·2023-05-17

    Mini Pound Cake Recalled for Undeclared Coconut Allergen

    Saint Lavian mini pound cake chocolate is being recalled because coconut is not listed on the ingredients label. Consumers with coconut allergies are at risk.

    Product
    Saint Lavian mini pound cake chocolate 2 pieces UPC: 4973341408841
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0875-2023·2023-05-17

    Kajitani Food Cigar Fry Recalled for Unlabeled Coconut

    Kajitani food cigar fry (110g, UPC 4901332108289) contains coconut that is not declared on the label. The undeclared allergen poses a health risk to consumers with coconut allergies.

    Product
    Kajitani food cigar fry 110g UPC: 4901332108289
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0861-2023·2023-05-17

    Ajikal Kotsubukko Snack Recalled for Undeclared Coconut

    Ajikal 44g Kotsubukko snacks containing undeclared coconut were distributed across multiple US states and Canada. Consumers with a coconut allergy should not consume this product.

    Product
    Ajikal 44g Kotsubukko 4 series UPC: 4510656600708
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1569-2023·2023-05-17

    Aesculap Caiman Articulating Surgical Device Recalled for Loose Spring

    Aesculap Caiman Articulating electrosurgical devices are being recalled because a spring may become loose and fall out during surgery, potentially entering the patient's body.

    Product
    Aesculap Caiman Articulating D5/360MM - An electrosurgical cutting and coagulation device for cutting/coagulation/ablation during endoscopic (including laparoscopic, arthroscopic) surgery, and may in addition be intended for open surgery. Product Code: PL771SU
    Category
    Medical Device
    Distribution
    Distributed nationwide