The Recall Desk

State

American Samoa product recalls

72,907 recalls have nationwide distribution and so reach American Samoa. 25 additional recalls listed American Samoa specifically in their distribution scope.

What the numbers show

Total
25
Critical
1
Severe
5
Most recent
2026-09-09

Of the 25 recalls naming American Samoa we have scored against our rubric, 1 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 5 (20%) are Severe.

Which agencies issued them

These figures cover only the 25 recalls whose distribution notice names American Samoa specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1251–1275 of 72932

  • HighNHTSA·26V400000·2026-06-23

    Hyundai Tucson instrument panel displays may fail due to software error

    Hyundai is recalling certain 2025-2026 Tucson, Tucson Hybrid and Tucson Plug-In Hybrid vehicles because a software error may cause the instrument panel display to fail.

    Product
    HYUNDAI — HYUNDAI TUCSON PLUG-IN HYBRID, TUCSON HYBRID, TUCSON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E036000·2026-06-19

    Airxcel Recalls MaxxAir N-Series Maxxfan Fans Due to Overheating Risk

    Airxcel is recalling MaxxAir N-Series Maxxfan rooftop ventilation fans because the printed circuit board may overheat, increasing the risk of a fire.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V397000·2026-06-19

    Indian Motorcycle Recalls 2026 Chief Vintage for Incorrect Rim Labeling

    Indian Motorcycle is recalling 2026 Chief Vintage models because the VIN label lists the wrong rear rim width, which could lead to improper tire mounting and loss of control.

    Product
    INDIAN — INDIAN CHIEF VINTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26562·2026-06-18

    GOPO Toys pull string teething toys reported to cause choking incidents

    About 70,410 GOPO Toys pull string teething toys are being recalled after three reports of the silicone strings reaching the back of a child's throat, causing respiratory distress or choking.

    Product
    GOPO TOYS Pull String Teething Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26563·2026-06-18

    Arrogantf Spa Drain Covers Recalled Over Entrapment and Drowning Hazards

    Arrogantf spa drain covers sold on Amazon violate federal safety standards and pose entrapment and drowning hazards. Consumers should stop using them immediately and contact the importer for a refund.

    Product
    Arrogantf Spa Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V394000·2026-06-18

    2026–2027 Cadillac Vistiq Third-Row Seat Power Fold Feature Recall

    General Motors is recalling 2026–2027 Cadillac Vistiq vehicles because the third-row power seatback may fail to reverse when it encounters a person, potentially trapping them.

    Product
    CADILLAC — CADILLAC VISTIQ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V393000·2026-06-18

    2026 Subaru Solterra battery electric vehicles loss of drive power

    Toyota Motor Engineering & Manufacturing is recalling 2026 Subaru Solterra vehicles due to a fault in the battery electronic control unit that may cause loss of drive power, increasing crash risk.

    Product
    SUBARU — SUBARU, TOYOTA, LEXUS SOLTERRA, BZ, RZ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26561·2026-06-18

    BABESIDE doll and stroller toy sets violate the small parts ban

    About 2,200 BABESIDE doll and stroller toy sets are being recalled because the small pacifier violates the small parts ban and the plush bear's eyes can detach.

    Product
    BABESIDE Doll and Stroller Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26567·2026-06-18

    Children's Pajamas Recalled by SHEIN Over Burn Hazard

    SHEIN Distribution Corporation is recalling about 160 Michley children's pajamas that violate the mandatory flammability standard for children's sleepwear, posing a burn injury or death risk. No injuries have been reported.

    Product
    Michley Children's Pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26564·2026-06-18

    Veseacky Children's Pajama Sets Recalled for Burn Hazard

    Veseacky children's pajama sets are recalled due to burn hazards from violating mandatory safety standards for children's sleepwear. About 3,700 units were sold on Amazon from October 2020 through January 2026.

    Product
    Veseacky Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26565·2026-06-18

    Arizer Solo III vaporizers recalled after four battery explosion reports

    About 5,000 Arizer Solo III Intergalactic (Black) portable vaporizers are being recalled after four reports of the internal lithium-ion battery exploding or igniting.

    Product
    Arizer Solo III portable electronic vaporizers (Intergalactic/Black color only)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V395000·2026-06-18

    Farber Specialty Recalls 2025-2026 Emergency Vehicles Due to Touchscreen Failure

    Farber Specialty is recalling 2025-2026 HX620 and MCXCR emergency vehicles because the touchscreen may fail, preventing the activation of exterior lights and emergency equipment.

    Product
    FARBER SPECIALTY — FARBER SPECIALTY MCXCR, HX620 SBA 6X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26568·2026-06-18

    Joolz Aer2 car seat adapters can detach, allowing the seat to fall

    About 3,840 Joolz Aer2 Car Seat Adapters are being recalled because they can fail to attach properly to the stroller, which may allow the car seat to fall.

    Product
    Joolz Aer2 Car Seat Adapters for Joolz Aer 2 Stroller
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0580-2026·2026-06-17

    Doxorubicin liposome injection vials contain glass particulate matter

    Doxorubicin Hydrochloride Liposome Injection, 50 mg/25 mL single-dose vials, is being recalled because of particulate matter identified as glass. 675 vials are affected.

    Product
    DOXORUBICIN HYDROCHLORIDE — DOXORUBICIN HYDROCHLORIDE (DOXORUBICIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0620-2026·2026-06-17

    Beekeeper's Naturals saline nasal spray recalled for microbial contamination

    Beekeeper's Naturals Saline Nasal Spray with propolis and xylitol, 1 fl oz, is being recalled for microbial contamination of non-sterile products. 1,680 bottles are affected.

    Product
    BEEKEEPER'S NATURALS Saline Nasal Spray, Sinus Congestion Rinse, Made with Propolis + Xylitol, 1 FL OZ (30 mL) per bottle, Manufactured For: Beekeeper's Naturals USA Inc., Covina, CA 91789.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0595-2026·2026-06-17

    Gas-X Extra Strength softgels contaminated with propylene glycol machine coolant

    Gas-X Extra Strength simethicone 125 mg softgels are being recalled because of contamination with a diluted propylene glycol-based coolant leaked from a machine during packaging.

    Product
    Gas-X Extra Strength, SIMETHICONE 125 mg/ANTIGAS, packaged in a) 120 SoftGels (UPC 3 00674 35041 9, b) 72 SoftGels (UPC 3 00439 00572 1), Distributed by: Haleon, Warren, NJ 07059.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0942-2026·2026-06-17

    Moringa green superfood capsules may be contaminated with Salmonella

    TNVitamins and Doctor's Pride moringa green superfood capsules are being recalled because the product may be contaminated with Salmonella. 13,000 bottles are affected.

    Product
    1. TNVitamins Ultrapotent Complete Green Superfood Moringa Capsules (120 count) 2. Doctor s Pride Complete Green Superfood Ultra Potent Moringa 10,000 mg (120 capsules)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2316-2026·2026-06-17

    GE Allia IGS 7 Pulse systems pose shock risk to servicers

    Allia IGS 7 Pulse angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on. 35 units affected.

    Product
    Allia IGS 7 Pulse angiographic X-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2333-2026·2026-06-17

    CORFLO Safety PEG kit 30-4320 contains recalled lidocaine injection

    CORFLO Safety PEG Kits, catalog number 30-4320, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 231 kits are affected.

    Product
    Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-4320
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2406-2026·2026-06-17

    MOSAIQ oncology software may fail to load adapted treatment plan

    The MOSAIQ Oncology Information System is being recalled because the software may fail to load an adapted baseline shift plan during treatment delivery when a communication error occurs.

    Product
    MOSAIQ Oncology Information System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2413-2026·2026-06-17

    Orca single use endoscope valves recalled over sticking suction buttons

    Boston Scientific is removing Orca Sterile, Single Use Air/Water and Suction Valves because of a higher than anticipated occurrence of the suction button sticking. 9,750 units affected.

    Product
    Orca Single Use Air/Water and Suction Valves, Material Number (UPN) SUV-617-50; The Orca Air/Water Valve is intended to be used to control the air/water function on an endoscope during a GI (gastrointestinal) endoscopic procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide