The Recall Desk

State

American Samoa product recalls

73,100 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 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

11926–11950 of 73125

  • ModerateFDA (Devices)·Z-1386-2024·2024-04-03

    Philips Patient Information Center Custom Ringtones Fail When Screen Locked

    Philips Patient Information Center iX running software version 4.X may not play custom ringtones when iOS screens are locked with a passcode. Approximately 257,183 units have been distributed worldwide. No injuries have been reported.

    Product
    Patient Information Center iX (PIC iX), Model Numbers 866389, 866390 (PIC iX Expand), and 866424 (PIC iX Hardware) running Software Version Number 4.X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1363-2024·2024-04-03

    Thermalon Neck Wrap recalled due to potential mold and mildew growth

    Bruder Healthcare Company is recalling Thermalon Neck Wrap (Item Number 24322) from certain lots due to potential mold and mildew growth from excessive moisture exposure. Consumers should discontinue use and contact the manufacturer.

    Product
    Thermalon Neck Wrap, Item Number 24322
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1387-2024·2024-04-03

    CareEvent Event Management System notification failure on locked iOS devices

    The CareEvent Event Management System's Care Assist mobile application fails to play custom ringtones when iOS device screens are locked with a passcode. This may result in missed alerts or notifications.

    Product
    CareEvent Event Management System, Model Numbers 866435 and 866436 (CareEvent Upgrade), Software Version Number C.03.X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0427-2024·2024-04-03

    FDA Recalls VCF Contraceptive Film Due to Manufacturing Process Violations

    The FDA is recalling VCF Contraceptive Film due to manufacturing process deviations. Apothecus Pharmaceutical Corp. initiated the voluntary recall on March 21, 2024, affecting 17,280 cartons distributed nationwide.

    Product
    VCF CONTRACEPTIVE — VCF CONTRACEPTIVE (NONOXYNOL-9)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1376-2024·2024-04-03

    Access Substrate Reagent Bottles Recalled for Missing Product Labels

    Beckman Coulter is recalling Access Substrate reagent bottles (REF 81906) due to missing product labels on certain manufacturing lots. While the missing labels may delay patient test result reporting, no incorrect results have been reported.

    Product
    Access Substrate, REF 81906, For use with the Access Immunoassay Systems
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V245000·2024-04-02

    2021 Jayco Redhawk motorhomes recalled for power steering connection defect

    Certain 2021 Jayco Redhawk motorhomes have a defective power steering connection that can cause sudden loss of power steering and brake assist, increasing crash risk. Dealers will replace the defective parts free of charge.

    Product
    ENTEGRA — ENTEGRA, JAYCO ESTEEM, ODYSSEY, GREYHAWK PRESTIGE, redundant ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V246000·2024-04-02

    2024 Hyundai Santa Fe rearview camera obstruction recall

    The rearview camera image may be obstructed by a trailer parking assist message, reducing rearward visibility and increasing crash risk. An over-the-air software update will fix the issue.

    Product
    HYUNDAI — HYUNDAI SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V244000·2024-04-01

    2023 Kia Forte: Front Suspension Control Arm Failure Risk

    Kia recalls certain 2023 Forte vehicles because the right front lower control arm may be improperly welded and fail, risking sudden loss of steering control and crashes.

    Product
    KIA — KIA FORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V243000·2024-03-29

    Big Tex Recalls 2024 Trailers Due to Brake Oil Leak Risk

    Big Tex Trailer Manufacturing is recalling 2024 25GN, 25PH, 3XGN, and 3XPH trailers because improperly installed oil seals may leak onto the brake system, increasing crash risk.

    Product
    BIG TEX — BIG TEX 25PH, 3XPH, 25GN, 3XGN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·24175·2024-03-28

    Stateside Bead Supply Magnetic Beads Recalled for Ingestion Hazard

    Stateside Bead Supply is recalling high-powered 5mm magnetic beads sold online from November 2022 through June 2023 because they violate federal magnet safety regulations and pose an ingestion hazard. If swallowed, the magnets can lodge in the digestive system and cause serious injury or death.

    Product
    Magnetic Beads HIGH POWER 5mm
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V238000·2024-03-28

    Chrysler minivan windshields may not be properly bonded to the vehicle

    Chrysler is recalling certain 2024 Pacifica and Voyager vehicles whose windshields may not have been properly bonded, allowing them to detach during a crash. This fails FMVSS 212.

    Product
    CHRYSLER — CHRYSLER VOYAGER, PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V237000·2024-03-28

    Chevrolet Colorado and GMC Canyon front wheel hub bolts may break

    General Motors is recalling certain 2023 Chevrolet Colorado and GMC Canyon vehicles because front wheel hub bolts may have been over-tightened and damaged during installation.

    Product
    CHEVROLET — CHEVROLET, GMC COLORADO, CANYON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24177·2024-03-28

    BJ's Wholesale Club Recalls Berkley Jensen 72-inch Tiki Torches for Burn Hazard

    BJ's Wholesale Club is recalling about 90,000 Berkley Jensen Citronella 72-inch Tiki Torches because the torch top can break open or fall off while lit, creating a burn hazard. The company has received nine reports of the top breaking or falling, including two burn injuries.

    Product
    Berkley Jensen Citronella 72-inch Tiki Torches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24742·2024-03-28

    Forias Pack and Play Mattresses Recalled for Infant Suffocation Hazard

    Forias pack and play mattresses sold on Amazon.com from May through August 2023 violate federal crib mattress safety standards and pose a suffocation hazard to infants. The product is missing required warnings and labels.

    Product
    Forias Pack and Play Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V239000·2024-03-28

    Jeep Cherokee turn signals may not self-cancel after a turn

    Chrysler is recalling certain 2022 Jeep Cherokee vehicles because the turn signal self-cancelling feature may not work properly, failing FMVSS 108.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V241000·2024-03-28

    Micro Bird Recalls One 2019 G5 Transit Bus for Defrosting Defect

    Micro Bird is recalling one 2019 G5 Transit Bus because a module failure may disable the windshield defrosting system, reducing visibility.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V242000·2024-03-28

    Micro Bird Recalls 2019 G5 School Buses for Defrosting System Defect

    Micro Bird is recalling 2019 G5 school buses because a module failure may disable the windshield defrosting system, reducing driver visibility.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V240000·2024-03-28

    Chrysler minivan traction control does not work with cruise control active

    Chrysler is recalling certain 2024 Pacifica and Voyager vehicles because the traction control system does not function while cruise control is activated. A free software update is the remedy.

    Product
    CHRYSLER — CHRYSLER VOYAGER, PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24741·2024-03-28

    Polaris Model Year 2022–2023 Snowmobiles Recalled for Fire Hazard

    Polaris is recalling about 7,000 Model Year 2022–2023 snowmobiles equipped with PATRIOT BOOST engines because the fuel line between the fuel rails can leak, posing a fire hazard. Consumers should stop using the recalled snowmobiles and contact Polaris for a free repair.

    Product
    Model Year 2022-2023 Snowmobiles equipped with PATRIOT BOOST Engines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24176·2024-03-28

    Purefog High Density Natural Fog Juice Liquid Recalled for Mold Risk

    Pure Brands of California is recalling Purefog High Density Natural Fog Juice Liquid because the product can expire sooner than the printed expiration date, posing a mold-exposure risk to people with compromised immune systems, damaged lungs, or mold allergies.

    Product
    Purefog High Density Natural Fog Juice Liquids
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V233000·2024-03-27

    2025 Peterbilt and Kenworth Trucks Recalled Over Steering Gear Defect

    PACCAR is recalling certain 2025 Peterbilt and Kenworth trucks because the steering gear sector shaft may have been improperly heat-treated, which can cause the gear teeth to crack or fracture.

    Product
    PETERBILT — PETERBILT, KENWORTH 579, T680, T280, T380
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1300-2024·2024-03-27

    FDA Recalls HeartMate II Left Ventricular Assist Systems for Graft Obstruction

    Thoratec Corp. recalls HeartMate II left ventricular assist system kits due to outflow graft deformation that could obstruct blood flow. The FDA has classified this as a Class I recall affecting 2,240 units distributed worldwide.

    Product
    HeartMate II Left Ventricular Assist System (LVAS): 1. HeartMate II Sealed Outflow Graft with Bend Relief REF 103393 2. HeartMate II LVAS Implant Kit, US REF 106015 3. HeartMate II LVAS Implant Kit, OUS REF 106016 Update (February 14, 2024) HeartMate II Left Ventricular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V236000·2024-03-27

    Heartland RV Cooktop LED Backlight Circuit Fire Risk Recall

    Heartland is recalling 10,038 model year 2023-2024 fifth wheels and travel trailers because the LED backlight circuit board in the cooktop range may fail and overheat, increasing the risk of a fire.

    Product
    HEARTLAND — HEARTLAND PROWLER, SOUTH FORK, SUNDANCE, MALLARD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0393-2024·2024-03-27

    FDA Recalls Unapproved Tianeptine Elixir Drug Product Nationwide

    Neptune's Fix Tianeptine Elixir, distributed nationwide by Super Chill Products, is recalled because it contains tianeptine, a substance not approved by the FDA for any medical use in the United States. Consumers should not use this product.

    Product
    Neptune's Fix, Tianeptine Elixir, Fast Acting, 0.338 fl.oz. (10 mL) bottle, Distributed By Superchill Products, 827 6th Avenue, New York, New York 10001.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1301-2024·2024-03-27

    HeartMate 3 Left Ventricular Assist System recalled for outflow graft obstruction

    The FDA is recalling the HeartMate 3 Left Ventricular Assist System due to observed outflow graft deformation that can obstruct blood flow. Patients with implanted devices should contact their healthcare provider.

    Product
    HeartMate 3 Left Ventricular Assist System (LVAS): 1. HeartMate 3 Sealed Outflow Graft with Bend Relief, Investigational Device Exemption (IDE) 2. HeartMate 3 Sealed Outflow Graft with Bend Relief, US 3. HeartMate 3 Sealed Outflow Graft with Bend Relief, OUS 4. HeartMate 3…
    Category
    Medical Device
    Distribution
    Distributed nationwide