The Recall Desk

State

American Samoa product recalls

73,388 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
9
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 9 (36%) are Severe.

Which agencies issued them

These figures cover only the 25 recalls whose distribution notice names American Samoa specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22026–22050 of 73413

  • SevereNHTSA·22E005000·2022-01-28

    Samsung SDI Recalls High Voltage Battery Packs for Sudden Power Loss

    Samsung SDI is recalling specific high voltage battery packs that may fail, causing a sudden loss of drive power and increasing crash risk.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V042000·2022-01-28

    Mercedes-Benz Recalls 2021 AMG GT Black Series for Wiring Harness Defect

    Mercedes-Benz is recalling 2021 AMG GT Black Series vehicles because an incorrectly sized front wheel speed sensor wiring harness may damage, impairing safety systems and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V040000·2022-01-28

    2021-2022 Porsche Cayenne Rear Axle Alignment Safety Recall

    Porsche is recalling 2021-2022 Cayenne vehicles due to potential rear axle misalignment following prior repairs. The defect may cause premature tire wear and increase crash risk.

    Product
    PORSCHE — PORSCHE CAYENNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V041000·2022-01-28

    2022 Forest River Vengeance Trailers Recalled for Incorrect Tire Pressure Labels

    Forest River is recalling certain 2022 Vengeance Fifth Wheel trailers because the tire pressure labels may display incorrect information for the front tires, which could result in under-inflated tires and increase the risk of a crash.

    Product
    FOREST RIVER — FOREST RIVER VENGEANCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V038000·2022-01-28

    2013-2021 Grand Design recreational vehicles recalled for fire hazard

    Grand Design RVs (2013-2021) are recalled for an improperly secured 110-volt refrigerator wire that may cause electrical arcing and fire. Dealers will inspect and replace damaged wiring at no cost.

    Product
    GRAND DESIGN — GRAND DESIGN SOLITUDE, REFLECTION, MOMENTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22718·2022-01-28

    Matrix T1 and T3 Commercial Treadmills Recalled for Fire Hazard

    Johnson Health Tech is recalling about 19,900 Matrix T1 and T3 Series commercial treadmills because the power cord can become loose from the power socket, causing sparking, smoking, melting, and fire. No injuries have been reported.

    Product
    Matrix T1 and T3 Series Commercial Treadmills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateNHTSA·22V039000·2022-01-28

    2020-2021 Grand Design Imagine Trailers Recalled for Sharp Cabinet Handles

    Grand Design is recalling 2020-2021 Imagine travel trailers with cast aluminum cabinet handles that may have sharp edges. The sharp edges could cut or scrape occupants, and dealers will replace the handles free of charge.

    Product
    GRAND DESIGN — GRAND DESIGN IMAGINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E004000·2022-01-27

    Prevost Recalls Seat Brackets That May Fail in Crashes

    Prevost is recalling certain seat brackets that may not meet strength requirements, increasing injury risk in a crash.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V037000·2022-01-27

    Tesla Vehicles: Full Self-Driving Software May Skip Required Stops

    Tesla is recalling certain 2016-2022 Model S and X, 2017-2022 Model 3, and 2020-2022 Model Y vehicles. The Full Self-Driving (Beta) software rolling stop feature may allow vehicles to pass through all-way stop intersections without stopping, increasing crash risk.

    Product
    TESLA — TESLA MODEL S, MODEL X, MODEL 3, MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V035000·2022-01-27

    RAM 2500-5500 Recall for Windshield Wiper Arm Loosening

    Chrysler is recalling 2019-2020 RAM 2500-5500 vehicles because wiper arms may loosen, reducing visibility in certain weather conditions.

    Product
    RAM — RAM 2500, 4500, 3500, 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V036000·2022-01-27

    2021 Chevrolet Tahoe and other GM vehicles driveshaft failure recall

    GM recalls certain 2021 Tahoe, Suburban, Yukon, and Escalade vehicles for rear driveshaft assemblies with improperly heat-treated internal components that may fail, causing loss of drive power and increased crash risk.

    Product
    GMC — GMC, CHEVROLET, CADILLAC YUKON, YUKON XL, TAHOE, ESCALADE ESV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0450-2022·2022-01-26

    Medtronic HawkOne Atherectomy System Recalled for Tip Detachment and Embolization Risk

    Medtronic is recalling the HawkOne Directional Atherectomy System globally due to reports of tip damage that can detach and cause embolization. The device is used to remove arterial plaque in peripheral blood vessels.

    Product
    Medtronic HawkOne Directional Atherectomy System, Catalog numbers H1-M and H1-M-INT., Multi-vessel, 6F (2.2 mm) Recommended sheath, 0.014" (0.36 mm) Compatible guidewire. The HawkOne directional atherectomy system is intended for use in atherectomy of the peripheral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0462-2022·2022-01-26

    Semglee Insulin Glargine Prefilled Pens Missing Label

    Mylan Pharmaceuticals is recalling approximately 73,175 Semglee (insulin glargine) prefilled pens nationwide because some units have a missing label. Patients should check their pens and contact their pharmacist or doctor if affected.

    Product
    Semglee (insulin glargine) injection, 100 units/mL (U-100), 3 mL Prefilled Pen (NDC 49502-0196-71), packaged in Five 3 mL Prefilled Pens per carton (NDC 49502-0196-75), Rx only, Manufactured in Malaysia for: Mylan Specialty L.P., Morgantown, WV, 26505.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V032000·2022-01-26

    Pierce Fire Trucks Recalled for Fuel Tube Cracking and Leak Risk

    Pierce Manufacturing is recalling 2015-2021 Enforcer, Quantum, Velocity, and Arrow XT fire trucks because fuel tubes may crack and leak high-pressure fuel, increasing fire risk.

    Product
    PIERCE — PIERCE ENFORCER, QUANTUM, VELOCITY, ARROW XT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0377-2022·2022-01-26

    SENNA Syrup unit-dose cups recalled for microbial contamination

    Lohxa, LLC is recalling SENNA Syrup (sennosides) 8.8 mg/5 mL unit-dose cups due to microbial contamination of the non-sterile product. The recall affects Lot #AM1115S with expiration date 01/2023, distributed nationwide.

    Product
    SENNA Syrup (sennosides) 8.8 mg/ 5 mL unit-dose cups, packaged in 24 cups per carton, Mfg for: AvKARE, TN 38478, NDC 50262-731-24.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0451-2022·2022-01-26

    Medtronic HawkOne Directional Atherectomy Device Recalled for Tip Damage

    Medtronic is recalling 28,094 units of its HawkOne directional atherectomy system due to reports of catheter tip damage and detachment that can cause blood clots in blood vessels.

    Product
    Medtronic HawkOne Directional Atherectomy System, Catalog numbers H1-S and H1-S-INT, Small Vessel, 6F (2.2 mm) Recommended sheath, 0.014" (0.36 mm) Compatible guidewire. The HawkOne directional atherectomy system is intended for use in atherectomy of the peripheral vasculature.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V034000·2022-01-26

    Audi vehicles recalled for rear axle misalignment causing premature tire wear

    Certain 2019-2021 Audi vehicles are recalled for rear axle misalignment that may cause premature tire wear and increase crash risk. Dealers will inspect and adjust the alignment at no charge, replacing any worn tires as needed.

    Product
    AUDI — AUDI S5, A4 ALLROAD, S7, Q5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0501-2022·2022-01-26

    Draeger Fabius MRI Anesthesia Machines recalled due to misrouted oxygen hoses

    Draeger Medical recalls 26 Fabius MRI Anesthesia Machines due to incorrectly routed internal oxygen hoses. The misrouting can cause oxygen flow to deviate from set levels, risking inadequate patient oxygenation.

    Product
    Draeger Fabius MRI Anesthesia Machine, Catalog Number 8607300
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V033000·2022-01-26

    2021 Toyota Venza Hybrid rear turn signal lighting system failure recall

    Toyota is recalling certain 2021 Venza Hybrid vehicles due to water intrusion in rear turn signal lights, which can cause electrical short circuits and lighting failure, increasing crash risk.

    Product
    TOYOTA — TOYOTA VENZA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0513-2022·2022-01-26

    Dental implant kits recalled for mislabeled implant dimensions

    Straumann USA LLC is recalling certain Neodent Easypack dental implant kits due to mislabeling where packaging does not match the implant dimensions inside. Affected units contain 3.5x8mm implants instead of the labeled 3.5x13mm size.

    Product
    Neodent Easypack Helix GM Acqua 3.5X13/Smart 4.5X2.5 Article Number: 138.107
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22058·2022-01-26

    Eguana Technologies Evolve Home Energy Storage Systems Recalled for Fire Hazard

    Eguana Technologies is recalling about 245 Evolve Home Energy Storage Systems because the lithium-ion battery modules can overheat and pose a fire hazard. Consumers should contact the company immediately to schedule a free repair or battery replacement.

    Product
    Evolve Home Energy Storage Systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22060·2022-01-26

    Geri-Care Over-the-Counter Drugs Recalled for Non-Child-Resistant Packaging

    Geri-Care Pharmaceuticals is recalling about 800 bottles of over-the-counter acetaminophen and aspirin tablets because the packaging is not child resistant, posing a poisoning risk to young children.

    Product
    Over-the-counter drugs
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0504-2022·2022-01-26

    Gentueri Viral Transport Medium Recalled Due to Turbidity and Discoloration

    Gentueri Inc is recalling 4,150 units of Gentueri Viral Transport Medium (VTM) nationwide due to visual turbidity and discoloration that may compromise diagnostic samples in transit.

    Product
    Gentueri Viral Transport Medium (VTM), Sterile, IVD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0503-2022·2022-01-26

    VITROS High Sample Diluent A Reagent Produces Lower Than Expected Results

    Ortho-Clinical Diagnostics is recalling VITROS High Sample Diluent A Reagent Pack Lot 2190 because it produces lower than expected TSH test results. The recall affects 1,416 units distributed worldwide.

    Product
    VITROS Immunodiagnostic Products High Sample Diluent A Reagent Pack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0500-2022·2022-01-26

    ImagePilot diagnostic imaging software versions 1.92 and 1.93 measurement error recall

    Konica Minolta's ImagePilot versions 1.92 and 1.93 software may provide incorrect measurement calculations if improper power sequences are used with AeroDR or Momentum Panel systems.

    Product
    ImagePilot Versions 1.92 and 1.93-software primarily facilitates processing and presentation of medical images on display monitors for medical diagnostics Product number: ADFR and ADJC
    Category
    Medical Device
    Distribution
    Distributed nationwide