The Recall Desk

State

Alabama product recalls

72,820 recalls have nationwide distribution and so reach Alabama. 6,341 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total
6,341
Critical
1,121
Severe
1,337
Most recent
2026-09-02

Of the 6,341 recalls naming Alabama we have scored against our rubric, 1,121 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,337 (21%) are Severe.

These figures cover only the 6,341 recalls whose distribution notice names Alabama specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

676–700 of 79161

  • 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-0685-2026·2026-07-22

    Leader Carbamide Peroxide Earwax Removal Kit Recalled for Subpotency

    Bell Pharmaceuticals is recalling Leader Carbamide Peroxide 6.5% Earwax Removal Kit due to subpotency—the active ingredient is significantly reduced (approximately 0.6% versus the expected 6–7%) and the pH is low.

    Product
    LEADER EARWAX REMOVAL KIT EARWAX REMOVAL AID AND BULB — LEADER EARWAX REMOVAL KIT EARWAX REMOVAL AID AND BULB (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 (Food)·H-1152-2026·2026-07-22

    Liquid Hope Organic Meal Replacement Formula Subpotent Vitamin A Recall

    Nutricia North America is recalling Liquid Hope Organic Whole Foods Meal Replacement Peptide Formula Berry Medley because the product contains less vitamin A than labeled. A testing laboratory used an incorrect method that overstated the vitamin A concentration.

    Product
    functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY NET WT. 12 OZ (341g) case UPC 8 57858 00453 3, package UPC 8 57858 00450 2
    Category
    Food
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-2722-2026·2026-07-22

    da Vinci SP Instrument Arm Drape may detach during surgical procedures

    Intuitive Surgical is recalling da Vinci SP Instrument Arm Drapes because the drape rings may detach, exposing the instrument arm and potentially delaying procedures. The recall affects 11,113 units distributed worldwide.

    Product
    da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13, 430013-15
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0688-2026·2026-07-22

    CAREone Earwax Removal Drops Recalled for Subpotent Active Ingredient

    CAREone Earwax Removal Drops (Carbamide Peroxide 6.5%) are recalled because the product contains significantly reduced active ingredient (~0.6% vs. expected ~6–7%) and low pH, making it ineffective.

    Product
    CAREONE EARWAX REMOVAL DROPS — CAREONE EARWAX REMOVAL DROPS (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
  • 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 (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-0679-2026·2026-07-22

    Clinere Ear Wax Remover Recalled for Subpotent Carbamide Peroxide

    Bell Pharmaceuticals is recalling Clinere Ear Wax Remover nationwide because the product contains significantly reduced active ingredient and low pH. The affected lots were distributed throughout the United States.

    Product
    CLINERE EAR WAX REMOVER — CLINERE EAR WAX REMOVER (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·26V465000·2026-07-17

    Great Dane Recalls 2027 Champion Trailers for Rear Impact Guard Defect

    Great Dane is recalling 2027 Champion dry van trailers because they may lack required rear impact guard extension channels, increasing injury risk in crashes.

    Product
    GREAT DANE — GREAT DANE CHAMPION
    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
  • 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·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
  • SevereNHTSA·26V457000·2026-07-16

    Altec Recalls AP Series Trucks Due to Fire Risk

    Altec is recalling 2013-2025 AP45A trucks because a damaged wire in the cargo area can overheat and ignite flammable material, increasing the risk of fire.

    Product
    ALTEC — ALTEC AP SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26630·2026-07-16

    Adult Portable Bed Rails Recalled Due to Entrapment and Asphyxiation Risk

    MNIENT Adult Portable Bed Rails violate mandatory safety standards and pose risks of entrapment, asphyxiation, falls, and laceration. Consumers should stop using them immediately and contact the manufacturer for a refund.

    Product
    MNIENT Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26621·2026-07-16

    Nottaway Chandelier Fixtures recalled for electrocution hazard risk

    Currey & Company is recalling about 447 Nottaway chandeliers due to lack of proper electrical grounding, which poses a risk of serious injury or death from electrocution. Consumers should stop using them immediately and contact the company for a free replacement.

    Product
    Nottaway Chandelier Fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26627·2026-07-16

    Noerishia Adult Portable Bed Rails Recalled for Entrapment and Asphyxiation Risk

    Noerishia Adult Portable Bed Rails sold on Amazon violate the mandatory safety standard and pose a risk of serious injury or death from entrapment and asphyxiation. Users can become entrapped within the rail or between the rail and mattress.

    Product
    Noerishia Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide