The Recall Desk

State

Texas product recalls

73,596 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.

Which agencies issued them

These figures cover only the 12,438 recalls whose distribution notice names Texas specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29351–29375 of 86034

  • HighFDA (Devices)·Z-1181-2021·2021-03-17

    Getinge Flow i Anesthesia Systems Recalled for Absorber Docking Failures

    Getinge Group Logistics America is recalling 144 Flow i Anesthesia Systems due to complaints of incorrect FiCO2 readings and System Check Out failures when docking the absorber.

    Product
    Anesthesia gas-machine - Product Usage: intended for use in administering anesthesia while controlling the entire ventilation of patients with no ability to breathe, as well as in supporting patients with limited ability to breathe.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0334-2021·2021-03-17

    Westminster Cracker Inc. Recalls Oyster Crackers Due to Plastic Foreign Object

    Westminster Cracker Inc. is recalling specific oyster cracker products because they may contain hard plastic foreign objects. Consumers should check their pantries for the affected items.

    Product
    Old Cape Cod Soup and Chowder Oyster Crackers - 8oz Box, 12 per case - UPC 093215801005; Westminster Bakers Co. Soup & Snack Crackers - 8oz Box, 12 per case - UPC 093215200426; Westminster Bakers Co. Soup & Snack Crackers - 8oz Box, 6 per case - UPC 093215200426
    Category
    Food
    Distribution
    13 states
  • HighCPSC·21097·2021-03-17

    HOFISH Recalls Mattresses for Federal Flammability Standard Violation

    HOFISH is recalling 10-inch hybrid mattresses sold on Amazon.com because they fail to meet the mandatory federal flammability standard, posing a fire hazard.

    Product
    HOFISH 10-Inch Hybrid Certi-PUR Certified Foam and Pocket Spring Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V185000·2021-03-17

    2021 Hyundai Santa Fe Air Bag Child Detection System Defect

    2021 Hyundai Santa Fe vehicles have a defective Occupant Detection System that may fail to prevent air bag deployment when a child restraint is detected in the front passenger seat, increasing crash injury risk.

    Product
    HYUNDAI — HYUNDAI SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1202-2021·2021-03-17

    Thermo Fisher Recalls Cascadion Clinical Analyzer Due to Software Defect

    Thermo Fisher Scientific is recalling 19 Cascadion Clinical Analyzers because a software defect may cause false Vitamin D deficiency results.

    Product
    Cascadion SM Clinical Analyzer, REF 99990000 SN Type: 9910
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1178-2021·2021-03-17

    Dräger VentStar Basic Breathing Circuits Recalled for Detachment Risk

    Draeger Medical is recalling 1,525 VentStar Basic breathing circuits because a Y-piece may detach, causing a leak that hinders patient ventilation.

    Product
    VentStar Basic (N) 180- Drager Breathing Circuits/Anesthesia Sets Order Number: MP00353 - Product Usage: Breathing circuit for conduction of respiratory gases between anesthesia machine or ventilator and patient. Intended for single use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0337-2021·2021-03-17

    Hu Chocolate-Covered Hunks Recalled for Undeclared Almonds

    Hu Products LLC is recalling Chocolate-Covered Hunks Sour Goldenberries because the product may contain undeclared almonds.

    Product
    Hu***CHOCOLATE-COVERED HUNKS SOUR GOLDENBERRIES***Net Wt. 4 oz (113g); packaged in a black bag; Distributed by: Hu Products LLC, NY, NY 10011
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1187-2021·2021-03-17

    Tosoh Thyroglobulin Antibody Calibrator Recalled for Calibration Failures

    Tosoh Bioscience Inc is recalling specific lots of Thyroglobulin Antibody Calibrators because some combinations with AIA PACKS resulted in unacceptable calibration values.

    Product
    Thyroglobulin Antibody (TgAB) Calibrator - Product Usage: intended for IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of anti-thyroglobulin antibodies (TgAb) in human serum on specific TOSOH AIA System analyzers. Measurements obtained by this device aid in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1189-2021·2021-03-17

    Physio-Control Recalls LIFEPAK CR2 Defibrillators Due to Missing Lid Magnets

    Physio-Control is recalling 89,763 LIFEPAK CR2 defibrillators because missing lid magnets may cause premature battery depletion.

    Product
    PHYSIO CONTROL LIFEPAK CR2 Defibrillator 3321605-xxx The LIFEPAK CR2 defibrillator is designed for indoor and outdoor use in a stationary environment. After the electrode pads are applied, the fully automatic model evaluates the heart rhythm and, if a shockable rhythm is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1188-2021·2021-03-17

    Siemens Dimension Vista HDLC Reagent Cartridges Recalled for Erroneous Results

    Siemens Healthcare Diagnostics is recalling Dimension Vista HDLC reagent cartridges due to discolored reagents that may cause erroneous test results.

    Product
    Dimension Vista HDLC - colorimetric method, lipoproteins - Product Usage: used as an aid in the diagnosis of lipid disorders (such as diabetes mellitus), various liver and renal diseases, and in the assessment of risk for atherosclerosis and cardiovascular disease.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1184-2021·2021-03-17

    MedComp Recalls Power Injectable CT Port Kits with Incorrect Port Size

    Medical Components, Inc. is recalling 96 Power Injectable CT Port kits because they contain 6.6F ports instead of the correct 5F size, which may prolong surgical procedures.

    Product
    Power Injectable CT Port insertion kits - Product Usage: is an implantable access device designed to provide repeated access to the vascular system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0299-2021·2021-03-17

    Ferring Recalls Menopur Due to Out-of-Specification pH in Diluent

    Ferring Pharmaceuticals is recalling Menopur (menotropins) and its 0.9% Sodium Chloride diluent because the diluent failed pH specifications. The recall covers products distributed nationwide in the USA.

    Product
    MENOPUR — MENOPUR (MENOTROPINS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0332-2021·2021-03-17

    One Degree Organic Foods Recalls Gluten Free Sprouted Rolled Oats

    One Degree Organic Foods is recalling 448,720 packages of Gluten Free Sprouted Rolled Oats due to rancidity and packaging integrity defects.

    Product
    One Degree Organic Foods Gluten Free Sprouted Rolled Oats NET WT. 5 lbs (80 oz) 2.27 kg UPC:6 75625 32318 8
    Category
    Food
    Distribution
    11 states
  • LowFDA (Devices)·Z-1183-2021·2021-03-17

    OraSure Methamphetamine Test Kit Recalled for Incorrect Reagent Lot Labeling

    OraSure Technologies is recalling 16 units of Methamphetamine Intercept Microplate kits due to a labeling error where the wrong lot number was printed on the box.

    Product
    Methamphetamine Intercept Microplate kit EIA - IVD qualitative determination of methamphetamine in oral fluid, PN 11041C.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V180000·2021-03-16

    Jayco Recalls 2021 Embark and Reatta Motorhomes Due to Gas Leak Risk

    Jayco is recalling 2021 Embark and Entegra Reatta motorhomes because an incorrectly routed LP furnace hose may cause a gas leak, increasing the risk of fire or explosion.

    Product
    JAYCO — JAYCO, ENTEGRA EMBARK, REATTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V181000·2021-03-16

    Peterbilt 536 Recalled for Engine Control Module Software Defect

    PACCAR is recalling one 2021 Peterbilt 536 truck because incorrect engine software may prevent safety features like braking and stability control from functioning properly.

    Product
    PETERBILT — PETERBILT 536
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V179000·2021-03-16

    Highland Ridge RV Recalls Fifth Wheels and Travel Trailers Due to Gas Leak Risk

    Highland Ridge RV is recalling 2019-2020 fifth wheels and travel trailers because an overtightened bolt may damage the stove's O-ring seal, causing a gas leak and increasing fire risk.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW MESA RIDGE, OPEN RANGE, SILVERSTAR, HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V178000·2021-03-16

    2021 Keystone Cougar Trailers Recalled for Electrical Shock Hazard in Inverter

    Certain 2021 Keystone Cougar trailers equipped with the Off the Grid Solar package may have an incorrectly wired inverter that energizes the shore power connection, posing an electrical shock risk. Keystone will repair the inverter at no charge.

    Product
    KEYSTONE — KEYSTONE COUGAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V176000·2021-03-15

    2021 BMW 430i and M440i side-thorax airbags may fail to deploy

    2021 BMW 430i and M440i models have defective side-thorax airbags that may not deploy during side-impact crashes, increasing injury risk. Owners should contact their dealer for a free software update.

    Product
    BMW — BMW M440I, 430I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V177000·2021-03-15

    Ditch Witch Trailers Recalled for Missing Side Reflectors

    Charles Machine Works is recalling specific Ditch Witch trailers because they may be missing side reflex reflectors, which reduces visibility to other drivers.

    Product
    DITCH WITCH — DITCH WITCH ZS6S, S4S, 745-7900, 025-1020
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V174000·2021-03-12

    ARBOC Specialty Vehicles Recalls 2021 Spirit of Freedom Due to Fuel Leak

    ARBOC is recalling 29 units of the 2021 Spirit of Freedom because a fuel hose may not be secured correctly, creating a fire risk.

    Product
    ARBOC SPECIALTY VEHICLES — ARBOC SPECIALTY VEHICLES SPIRIT OF FREEDOM
    Category
    Vehicle
    Distribution
    Distributed nationwide