The Recall Desk

State

Texas product recalls

72,820 recalls have nationwide distribution and so reach Texas. 12,385 additional recalls listed Texas specifically in their distribution scope.

What the numbers show

Total
12,385
Critical
1,703
Severe
2,405
Most recent
2026-09-06

Of the 12,385 recalls naming Texas we have scored against our rubric, 1,703 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,405 (19%) are Severe.

Which agencies issued them

These figures cover only the 12,385 recalls whose distribution notice names Texas specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

701–725 of 85205

  • ModerateFDA (Devices)·Z-2731-2026·2026-07-22

    Orthofix Articulated Minirail Fixator devices recalled for incorrect labeling

    Orthofix U.S. LLC is recalling Articulated Minirail Fixator external fixation devices due to incorrect model labeling. Three models were mislabeled: M101 labeled as M103, M103 labeled as M101, and M122 labeled as M111.

    Product
    Orthofix ARTICULATED MINIRAIL FIXATOR HORIZONTAL AXIS REF: M111, Unilateral orthopedic/trauma external fixation device
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Drugs)·D-0683-2026·2026-07-22

    Family Wellness Carbamide Peroxide Earwax Removal Kit Subpotent Drug

    Family Wellness Carbamide Peroxide 6.5% earwax removal kits are being recalled because they are subpotent with low pH and significantly reduced active ingredient content (approximately 0.6% versus the expected 6–7%). Consumers should stop using affected lots and consult their pharmacist.

    Product
    FAMILY WELLNESS EARWAX REMOVAL EARWAX AND BULB — FAMILY WELLNESS EARWAX REMOVAL EARWAX AND BULB (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2733-2026·2026-07-22

    Papablic Replacement Brush Heads Recalled for Potential Breakage

    Papablic Inc is recalling certain Papablic18B replacement brush head packs because the brush heads may break during use.

    Product
    Papablic Replacement Brush Heads. Model Number: Papablic18B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2734-2026·2026-07-22

    Papablic Replacement Brush Heads Recalled Due to Breakage Risk

    Papablic Inc is recalling Papablic Replacement Brush Heads (Model PAPA317AA) due to potential for brush heads to break. The recall affects approximately 13,400 packs distributed nationwide.

    Product
    Papablic Replacement Brush Heads. Model Number: PAPA317AA.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0687-2026·2026-07-22

    Meijer Earwax Removal Kit Recalled for Subpotent Active Ingredient

    Bell Pharmaceuticals is recalling Meijer Earwax Removal Kit (Carbamide Peroxide 6.5%) due to subpotency: the product contains significantly reduced active ingredient (~0.6% vs. expected ~6–7%) and low pH, limiting effectiveness.

    Product
    MEIJER EARWAX REMOVAL KIT — MEIJER EARWAX REMOVAL KIT (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2743-2026·2026-07-22

    Photera 600 Phototherapy Device UV Sensor Calibration Error

    Daavlin Distributing Company is recalling 26 Photera 600 phototherapy devices nationwide because the UV sensor gain calibration is incorrect, causing inaccurate ultraviolet output readings.

    Product
    Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-1153-2026·2026-07-22

    Nutricia NOURISH Organic Meal Replacement Powder Recalled for Low Vitamin A

    Nutricia North America is recalling its NOURISH ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY because testing showed the product contains less vitamin A than the label states. A laboratory error led to inaccurate test results that overstated the actual vitamin A concentration in the product.

    Product
    functional formularies NOURISH ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY COMPLETE PLANT BASED NUTRITION NET WT. 12 OZ (341g) case UPC 8 57858 00445 8, package UPC 8 57858 00447 2
    Category
    Food
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-2737-2026·2026-07-22

    Medline Kits with Zimmer Biomet Mixing Bowls and Spatulas Recalled

    Medline Industries is recalling 163 kits containing Zimmer Biomet mixing bowls and spatulas due to seal defects that risk sterility breach during surgical procedures.

    Product
    Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK-LF DYNJ61651J
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0681-2026·2026-07-22

    TopCare Earwax Removal Kit Recalled for Subpotent Drug Content

    Bell Pharmaceuticals is recalling TopCare Earwax Removal Kit (Carbamide Peroxide 6.5%) because the drug is subpotent with significantly reduced active ingredient (~0.6% vs. expected 6–7%) and low pH. The affected product was distributed nationwide.

    Product
    TOPCARE EARWAX REMOVAL KIT — TOPCARE EARWAX REMOVAL KIT (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0686-2026·2026-07-22

    Foster & Thrive Carbamide Peroxide 6.5% Recalled for Subpotent Strength

    Bell Pharmaceuticals recalls Foster & Thrive Carbamide Peroxide 6.5% due to subpotent drug substance with low pH and significantly reduced assay levels. Approximately 31,094 units distributed nationwide are affected.

    Product
    Foster & Thrive, Carbamide Peroxide 6.5%, 0.5 FL OZ (15 mL), NDC 70677-1154-01, Distributed by: McKesson Corp., via SSSL, Memphis, TN 38141.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0684-2026·2026-07-22

    Good Neighbor Pharmacy Earwax Removal Drug Recalled for Low Potency

    Bell Pharmaceuticals is recalling Good Neighbor Pharmacy Earwax Removal (Carbamide Peroxide 6.5%) due to subpotency—the active ingredient concentration is significantly reduced from expected levels, and the product has a low pH.

    Product
    GOOD NEIGHBOR PHARMACY EARWAX REMOVAL — GOOD NEIGHBOR PHARMACY EARWAX REMOVAL (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2729-2026·2026-07-22

    Orthofix MINIRAIL external fixation devices recalled for incorrect model labeling

    Orthofix U.S. LLC is recalling Orthofix MINIRAIL external fixation devices (Model M101) because they may be labeled with incorrect model numbers, potentially leading to use of wrong device specifications.

    Product
    Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number: M101, Unilateral orthopedic/trauma external fixation device
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Drugs)·D-0677-2026·2026-07-22

    Nystatin Cream Recall Due to Low Potency Test Results

    Padagis US LLC is recalling Nystatin Cream USP (100,000 USP units) because long-term stability testing found assay results below specification, meaning the product may contain less active ingredient than labeled.

    Product
    NYSTATIN — NYSTATIN (NYSTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0680-2026·2026-07-22

    Quality Choice Earwax Removal Kit Carbamide Peroxide Subpotent Drug Recall

    Bell Pharmaceuticals is recalling Quality Choice Earwax Removal Kit (Carbamide Peroxide 6.5%) due to subpotent drug content, with assay levels significantly reduced (approximately 0.6% versus expected 6–7%) and low pH levels.

    Product
    QUALITY CHOICE EARWAX REMOVAL KIT — QUALITY CHOICE EARWAX REMOVAL KIT (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0682-2026·2026-07-22

    Audiologist's Choice Carbamide Peroxide Earwax Removal Recalls

    Bell Pharmaceuticals is recalling Audiologist's Choice Carbamide Peroxide earwax removal product due to subpotency: the active ingredient concentration is approximately 0.6% instead of the expected 6–7%, and the product has low pH.

    Product
    AUDIOLOGISTS CHOICE EARWAX REMOVAL SYSTEM — AUDIOLOGISTS CHOICE EARWAX REMOVAL SYSTEM (CARBAMIDE PEROXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2740-2026·2026-07-22

    Rio II Nasal Pillows Interface Packaging and Labeling Discrepancy Recall

    3B Medical, Inc. is recalling Rio II Nasal Pillows Interface devices due to packaging and labeling discrepancies involving product size identification and device identifiers. The affected models are RII1001 (Small), RII1002 (Medium), and RII1003 (Large).

    Product
    Brand Name: Rio" II Product Name: Rio" II Nasal Pillows Interface Model/Catalog Number: RII1001 (Small), RII1002 (Medium), RII1003 (Large) Software Version: N/A Product Description: Nasal pillows interface intended for use with positive airway pressure therapy devices. The de
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V470000·2026-07-21

    Ford Recalls 2025-2027 Explorer and Lincoln Aviator for Seat Recline Issue

    Ford is recalling 76,748 2025-2027 Explorer and Lincoln Aviator vehicles because an unoccupied driver's seat may recline unintentionally, potentially trapping a second-row occupant.

    Product
    FORD — FORD, LINCOLN EXPLORER, AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowNHTSA·26V469000·2026-07-21

    Ember Recalls 2027 Travel Trailers Due to Incorrect VIN Labels

    Ember is recalling 2027 E-Series, Touring, and Overland travel trailers because the Federal Certification Label may list the wrong VIN, which could prevent owners from recognizing safety recalls.

    Product
    EMBER — EMBER E-SERIES, TOURING EDITION, OVERLAND SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V467000·2026-07-20

    Blue Bird Recalls 2022-2027 Vision Transit Buses for Brake Line Damage

    Blue Bird is recalling 2022-2027 Vision transit buses because an exhaust hanger pin may damage the hydraulic brake line, causing leaks and increasing fire or crash risks.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V466000·2026-07-20

    Blue Bird Vision School Buses Recalled Due to Brake Line Fire and Crash Risk

    Blue Bird is recalling certain 2022-2027 Vision school buses because an exhaust hanger cotter pin may damage hydraulic brake lines, causing leaks that increase the risk of fire or crashes.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V463000·2026-07-17

    Altec Recalls 2024-2026 AT Series Vehicles Due to Bearing Fastener Defect

    Altec is recalling 2024-2026 AT Series vehicles because turntable rotation bearing fasteners may not have been heat treated properly, posing a risk of component separation and injury.

    Product
    ALTEC — ALTEC AT SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26C004000·2026-07-17

    Evenflo Recalls Reo by Revolve360 Child Seats for Headrest Shift Risk

    Evenflo is recalling specific Reo by Revolve360 child seats because the headrest may shift during a crash, increasing injury risk.

    Product
    CHILD SEAT:SHELL:HEADREST:LOCKING MECHANISM recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V462000·2026-07-17

    Turtle Top Recalls 2026 Terra Ford Transit Buses Due to Lift Control Failure

    Turtle Top is recalling 2026 Terra Ford Transit buses because an electrical contactor may fail, preventing the wheelchair lift from stopping. This defect increases the risk of injury.

    Product
    TURTLE TOP — TURTLE TOP TERRA FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V464000·2026-07-17

    Foretravel Recalls 2027 Realm Motorcoaches Due to Fire Risk

    Foretravel is recalling 2027 Realm Presidential Motorcoaches because a fan assembly circuit board may overheat, increasing the risk of a fire.

    Product
    FORETRAVEL — FORETRAVEL REALM
    Category
    Vehicle
    Distribution
    Distributed nationwide