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.

Which agencies issued them

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.

701–725 of 79161

  • SevereCPSC·26625·2026-07-16

    Madewell Women's Sweaters Recalled for Serious Burn Injury Risk

    Madewell is recalling about 5,900 Double V-Neck Pullover and V-Neck Cardigan sweaters because they violate mandatory clothing textile standards and pose a risk of serious burn injuries or death. The firm received one report of a sweater catching on fire, though no injuries have been reported.

    Product
    Madewell Double V-Neck Pullover and V-Neck Cardigan Sweaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26617·2026-07-16

    Oitnlaughter LED Finger Lights Recalled for Battery Ingestion Risk

    Oitnlaughter LED Finger Lights sold on Amazon contain easily accessible button cell batteries that pose a risk of serious injury or death if swallowed by children. Consumers should stop using the toys immediately and contact Delightmi for a refund.

    Product
    Oitnlaughter LED Finger Lights
    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·26628·2026-07-16

    SDADI Kitchen Step Stools Recalled for Entrapment and Fall Hazards

    SDADI Kitchen Step Stools, models LT01 and LT05, can collapse or tip over and allow children's bodies to fit through openings, creating serious injury and death risks. Consumers should stop using them immediately and contact the importer for a refund.

    Product
    SDADI Kitchen Step Stools, models LT01 and LT05
    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·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
  • 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
  • HighNHTSA·26V456000·2026-07-16

    2026 Jeep Gladiator and Wrangler Steel Wheels Crack or Detach Recall

    Chrysler is recalling certain 2026 Jeep Gladiator and Wrangler vehicles because the steel wheels may be too thin and crack or detach, risking loss of vehicle control.

    Product
    JEEP — JEEP GLADIATOR, WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26624·2026-07-16

    Hollis 200LX Second Stage Diving Regulators Recalled for Drowning Risk

    Huish Outdoors recalls Hollis 200LX second stage diving regulators because the inlet tube can crack and break, posing a risk of serious injury or death from drowning. About 7,200 units are affected.

    Product
    Hollis 200LX Second Stage Diving Regulators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26626·2026-07-16

    Jobon butane torch lighters recalled for fire and burn hazards

    Jobon butane torch lighters sold online lack required child-resistant safety mechanisms and violate mandatory safety standards, posing risk of serious injury or death from fire and burn. Consumers should stop using them immediately.

    Product
    Jobon butane torch lighters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26629·2026-07-16

    Target Recalls Cat & Jack Children's Sandals for Choking Hazard Risk

    Target is recalling about 211,000 Cat & Jack Children's Sandals because decorative pearls can fall off and pose a choking hazard to children. No injuries have been reported.

    Product
    Cat & Jack Children's Sandals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26620·2026-07-16

    Boon PIVOT Collapsible Toddler Tower Kitchen Step Stools Recalled for Tip-Over Risk

    TOMY International is recalling approximately 116,908 Boon PIVOT Collapsible Toddler Tower Kitchen Step Stools due to a tip-over hazard that poses a risk of serious injury and death. The company has received 11 reports of the towers being unstable, shifting, or leaning, though no injuries have been reported to date.

    Product
    Boon PIVOT Collapsible Toddler Tower Kitchen Step Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26623·2026-07-16

    Space King Relic Lunch Box Copper Cups Recalled for Lead Poisoning Risk

    Warren James is recalling the copper cup found in Space King No Girls Allowed Relic Lunch Boxes due to high lead concentration levels that pose a lead poisoning hazard. Consumers should stop using the recalled cups immediately.

    Product
    Space King No Girls Allowed Relic Lunch Boxes (Cups only)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·26618·2026-07-16

    Panasonic Electric Toaster Ovens Recalled for Shock and Fire Hazards

    Panasonic is recalling about 11,480 Model NB-G200 Electric Toaster Ovens because the power cord insulation may be insufficient, posing a shock and fire risk. No fires or injuries have been reported, but four consumers reported tripped circuit breakers.

    Product
    Electric Toaster Ovens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2712-2026·2026-07-15

    Elekta Geneva Brachytherapy Applicator Intrauterine Tube Detachment Risk

    Elekta is recalling the Geneva Brachytherapy Applicator due to a safety concern that the tip of the intrauterine tube may detach and remain inside a patient during cancer treatment.

    Product
    Brand Name: Geneva Product Name: Brachytherapy Applicator Product Description: The device is intended for intracavitary brachytherapy for cancer treatment of the cervix and the endometrium. Optional needles can be placed for interstitial therapy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0673-2026·2026-07-15

    Bortezomib for Injection Recalled Due to Lack of Sterility Assurance

    Bortezomib for Injection 3.5mg/Vial manufactured by Reliance Life Sciences is being recalled nationwide due to lack of sterility assurance. Affected lots include RBIH0125A, RBIH0225A, RBIH0325A, and RBIH0525A distributed across the USA.

    Product
    Bortezomib for Injection 3.5mg/Vial, 10 mL per Single-Dose Vial, For Intravenous or Subcutaneous Use, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873. NDC: 70069-0836-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2711-2026·2026-07-15

    Brachytherapy Applicator Advanced Gynecological Applicator Tip Detachment

    Elekta, Inc. is recalling Advanced Gynecological Applicators due to potential detachment of the intrauterine tube tip, which may remain inside a patient during cancer treatment.

    Product
    Brand Name: Brachytherapy Applicator Product Name: Advanced Gynecological Applicator Product Description: The intended use of the Advanced Gynecological Applicator is intracavitary brachytherapy for cancer treatment of the cervix and endometrium. Optional needles can be placed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V453000·2026-07-15

    Orange EV Recalls Electric Trucks Due to Frame Rail Welding Defect

    Orange EV is recalling 2020-2026 electric trucks because improper welding may cause frame rails to crack and separate, increasing the risk of loss of control.

    Product
    ORANGE EV — ORANGE EV E-TRIEVER, HUSK-E, T-SERIES ELECTRIC TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2710-2026·2026-07-15

    Fletcher CT/MR Shielded Applicator Set for Gynecological Brachytherapy Recalled

    Elekta's Fletcher CT/MR Shielded Applicator Set is recalled due to risk that the tip of the intrauterine tube may detach and remain inside a patient during gynecological brachytherapy treatment.

    Product
    Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote Afterloading Applicator Product Description: The Fletcher CT/MR Shielded Applicator Set is intended for gynecological brachytherapy treatment of the cervix and endometrium.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0672-2026·2026-07-15

    Pemetrexed for Injection recalled due to lack of sterility assurance

    Reliance Life Sciences is recalling Pemetrexed for Injection 500mg/Vial nationwide due to lack of sterility assurance. The affected product may not meet required sterility standards for intravenous use.

    Product
    Pemetrexed for Injection 500mg/Vial, 1 50 mL Single-Dose Vial per carton, For intravenous use only, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0835-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0671-2026·2026-07-15

    Pemetrexed for Injection Recalled Due to Lack of Sterility Assurance

    Somerset Therapeutics is recalling Pemetrexed for Injection 100mg/Vial due to lack of sterility assurance. The recall affects approximately 12,000 vials distributed nationwide.

    Product
    Pemetrexed for Injection 100mg/Vial, 1 10 mL Single-Dose Vial per carton, For intravenous use only, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0834-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2716-2026·2026-07-15

    TMINI Tracking Array knob loosening causing potential array misalignment

    Think Surgical is recalling TMINI Femur and Tibia Tracking Arrays used in knee replacement surgery because the knob on the tracking array may loosen, causing potential misalignment of the array.

    Product
    TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code: M9461090040 TMINI Miniature Robotic System is indicated as a stereotaxic instrumentation system for total knee replacement (TKA) surgery. It is to assist the
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V454000·2026-07-15

    E-One Recalls Emergency Vehicles Due to Drive Mode Transfer Case Defect

    E-One is recalling 2025-2026 Cyclone N, Typhoon N, and Commercial emergency vehicles because the drive/pump mode transfer case may disengage, causing loss of rear-wheel power.

    Product
    E-ONE — E-ONE COMMERCIAL, TYPHOON N, CYCLONE N
    Category
    Vehicle
    Distribution
    Distributed nationwide