The Recall Desk

State

Texas product recalls

72,971 recalls have nationwide distribution and so reach Texas. 12,390 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total
12,390
Critical
1,705
Severe
2,407
Most recent
2026-09-16

Of the 12,390 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 12,390 recalls whose distribution notice names Texas specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6226–6250 of 85361

  • HighCPSC·25430·2025-08-14

    Remington hair dryers lack an immersion protection device against electrocution

    Remington brand hair dryers, model D3190DCDN, are being recalled because they lack an immersion protection device, posing a risk of electrocution or shock if dropped into water. About 56,300 units affected.

    Product
    Hair Dryers sold under the "Remington" brand, model number D3190DCDN
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25433·2025-08-14

    Children's spiral tower toys contain small balls banned for toddlers

    Three-tiered spiral children's tower toys are being recalled because the toy contains small balls and is intended for children under three, violating the small ball ban. About 260 units affected.

    Product
    Children's Spiral Tower Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25434·2025-08-14

    Firefly Safe and Green fuel bottles have a non child-resistant applicator

    Firefly Safe & Green 32 oz fuel bottles are being recalled because the nozzle applicator is not child-resistant as required for hydrocarbons, and the fuel is incorrectly labeled "Non-Toxic".

    Product
    Firefly Safe & Green 32 oz. Fuel Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2182-2025·2025-08-13

    BritePro Solo mini handles and blades may not illuminate as intended

    BritePro Solo Single-Use Fiber Optic Mini Handles and Blades in Macintosh and Miller sizes are being recalled because the handles may not illuminate as intended.

    Product
    BritePro Solo Single-Use Fiber Optic Mini Handle and Blade Ref: 040-02-0110U (Mac 1), 040-02-0120U (Mac 2), 040-02-0130U (Mac 3), 040-02-0131U (Mac 3 Strong Curve) 040-02-0140U (Mac 4), 040-02-0400U (Miller 00), 040-02-0410U (Miller 1), 040-02-0420U (Miller 2), 040
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0394-2025·2025-08-13

    Member's Mark freeze dried fruit packs tested positive for Listeria monocytogenes

    Member's Mark Freeze Dried Fruit Variety Pack 15 count is being recalled after the firm received positive test results for Listeria monocytogenes during routine testing. 21,552 boxes affected.

    Product
    Member's Mark FREEZE DRIED FRUIT VARIETY PACK 15 COUNT 5-0.35OZ (10g) STRAWBERRY POUCHES 5-0.42OZ (12g) BANANA POUCHES 5-0.25 OZ (10g) APPLE POUCHES NET WT 5.6OZ (160g) NO ADDED SWEETENERS ONE INGREDIENT ONLY PER PACK UPC 1 93968 50900 2
    Category
    Food
    Distribution
    44 states
  • SevereFDA (Devices)·Z-2179-2025·2025-08-13

    BD Alaris pump modules may perform outside established flow rate ranges

    BD Alaris Pump Module Model 8100 with Guardrails Suite MX software is being recalled because it may perform outside the established ranges for flow rate, bolus accuracy and occlusion alarm timing.

    Product
    BD Alaris Pump Module Model, 8100 with Guardrails, Suite MX software versions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2187-2025·2025-08-13

    BritePro Solo fiber optic laryngoscope handles may not illuminate properly

    BritePro Solo Single-Use Fiber Optic Laryngoscope Handles, REFs 040-310AU and 040-310U, are being recalled because the handles may not illuminate as intended.

    Product
    BritePro Solo Single-Use Fiber Optic Laryngoscope Handle Refs:040-310AU and 040-310U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2176-2025·2025-08-13

    Microbore extension sets are labeled as having an air eliminating filter

    Microbore Extension Sets with 0.2 Micron Filter are being recalled because the label indicates an air eliminating filter, but the filter fitted is not indicated for air removal. 34,825 US units affected.

    Product
    Microbore Extension Set with 0.2 Micron Filter. Catalog Number: V6215. for use with IV tubing.
    Category
    Medical Device
    Distribution
    32 states
  • SevereFDA (Devices)·Z-2129-2025·2025-08-13

    Plum Duo infusion system interface may become unresponsive during programming

    The Plum Duo Infusion System is being recalled because two sequences of programming events and alarm interactions may cause the user interface to become unresponsive. 4,677 units are affected.

    Product
    Plum Duo Infusion System, List Number: 400020401
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0379-2025·2025-08-13

    Bulk pecan pieces and halves recalled over potential Salmonella contamination

    Bulk pecan pieces and halves are being recalled because the pecans have the potential to be contaminated with Salmonella. 32,670 lbs are affected.

    Product
    FANCY MEDIUM PECAN PIECES 81124 561958 554707 6/13/2025 SDC1645 90 FANCY MEDIUM PECAN PIECES 81124 561965 554714 6/13/2025 SDC1645 90 FANCY MIDGET PECAN PIECES 81086 561845 554594 5/30/2025 SDC1505 56 FCY #15 HLVS 79291 561943 554692 5/21/2025 SDC1405 56 FANCY SMALL PECAN PIECES
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·H-0419-2025·2025-08-13

    Italian layer cake recalled because its pecans may carry Salmonella

    Item #1071 Italian layer cake is being recalled because the pecans used in it have the potential to be contaminated with Salmonella. The source does not state a quantity.

    Product
    Item #1071 Italian layer cake
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·H-0391-2025·2025-08-13

    Aral Silver Vobla dried roach fish recalled over Clostridium botulinum risk

    Aral Silver Vobla whole dried salted roach fish is being recalled because of Clostridium botulinum in uneviscerated fish. 23 boxes are affected across sixteen states.

    Product
    ARAL FISH; ARAL SILVER VOBLA; WHOLE DRIED, SALTED ROACH FISH EVISCERATED; FISH ROE DRIED; Ingredients: whole eviscerated dried roach fish, caviar may be present, salt.; Distributed by Krasnyi Oktyabr; PERISHABLE KEEP REFRIGERATED AT OR BELOW 40F; PRODUCT OF KAZAKHSTAN
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Devices)·Z-2180-2025·2025-08-13

    BD Alaris pump infusion sets may perform outside established flow ranges

    BD Alaris Pump Infusion Sets are being recalled because the pump module used with them may perform outside the established ranges for flow rate, bolus accuracy and occlusion alarm timing.

    Product
    BD Alaris Pump Infusion Sets REF: 10013186, BD Alaris Pump Infusion Set, Back Check Valve, 3 SmartSite Y-sites LVP 60D DEHP FREE 3SS CV; REF: 2452-0007, BD Alaris Pump Infusion Set, 2 Back Check Valves, 3 SmartSite Y-sitesAS LVP 10D 3SS 2CV; REF: 2204-0007, BD Alaris Pum
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V526000·2025-08-13

    Volkswagen Tiguan rear axle tie rod bolts may be loose

    Volkswagen is recalling certain 2025 Tiguan vehicles because a tie rod bolt on the rear axle assembly may be loose, which can lead to a loss of vehicle control. 15 vehicles are affected.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2186-2025·2025-08-13

    BritePro Solo mini laryngoscope handles may not illuminate as intended

    BritePro Solo Mini Single-Use Fiber Optic Laryngoscope Handles are being recalled because the handles may not illuminate as intended.

    Product
    BritePro Solo Mini Single-Use Fiber Optic Laryngoscope Handle REF:040-309U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2185-2025·2025-08-13

    BritePro Solo stubby laryngoscope handles may not illuminate as intended

    Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handles are being recalled because the handles may not illuminate as intended.

    Product
    Britepro Solo Stubby Single-Use Fiber Optic Laryngoscope Handle REF:040-03-0000U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2183-2025·2025-08-13

    BritePro Solo laryngoscope handles and blades may not illuminate as intended

    BritePro Solo Single-Use Fiber Optic Handles and Blades in Macintosh and Miller sizes are being recalled because the handles may not illuminate as intended.

    Product
    BritePro Solo Single-Use Fiber Optic Handle and Blade Refs: 040-331U (Mac 1), 040-332U (Mac 2), 040-333U (Mac 3), 040-335U (Mac 3.5) 040-334U (Mac 4), 040-341U (Miller 1), 040-342U (Miller 2), 040-343U (Miller 3), 040-344U (Miller 4), 040-361U (Phillips 1), 040-36
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2184-2025·2025-08-13

    BritePro Solo mini Miller blade handles may not illuminate as intended

    BritePro Solo Mini with Pro Miller Blade Size 1.5 is being recalled because the laryngoscope handles may not illuminate as intended.

    Product
    BritePro Solo Mini with Pro Miller Blade Size 1.5, REF:040-02-0415U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0574-2025·2025-08-13

    Spironolactone 25 mg tablets recalled after aluminum was found in product

    Spironolactone Tablets USP 25 mg are being recalled because of the presence of a foreign substance identified as aluminum. 11,328 bottles are affected.

    Product
    SPIRONOLACTONE — SPIRONOLACTONE (SPIRONOLACTONE)
    Category
    Drug
    Distribution
    Distributed nationwide