The Recall Desk

State

American Samoa product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43376–43400 of 73834

  • SevereUSDA FSIS·049-2017·2017-05-12

    Valley Innovative Services Recalls Frozen Entrée Products Due to Listeria Risk

    Valley Innovative Services is recalling approximately 130,071 pounds of frozen entrée products containing waffles due to possible Listeria monocytogenes contamination.

    Product
    Valley Innovative Services Recalls Meat and Poultry Frozen EntrÇe Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·17151·2017-05-12

    Honeywell Recalls SWIFT Wireless Gateways for Fire Alarm Communication Failures

    Honeywell is recalling SWIFT wireless gateways sold with fire alarm systems because they may fail to communicate with detectors during a fire, leaving occupants unalerted.

    Product
    SWIFT wireless gateway sold with fire alarm systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V318000·2017-05-12

    Can-Am Recalls 2017 Spyder RT Motorcycles for Headlight Beam Issue

    Bombardier is recalling 2017 Can-Am Spyder RT motorcycles because a manufacturing error may cause headlights to shine too high, potentially blinding oncoming traffic.

    Product
    CAN-AM — CAN-AM SPYDER RT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17746·2017-05-12

    Little Passports Recalls Science Kits Due to Battery Burn Hazard

    Little Passports is recalling Science Expeditions Northern Lights kits because the included battery packs can overheat and cause burns. No injuries have been reported.

    Product
    Science Expeditions Northern Lights science kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V311000·2017-05-11

    Toyota Recalls Tundra and Sequoia for Cracking Lugnuts

    Toyota is recalling 2013-2017 Tundra and Sequoia vehicles with specific aftermarket wheels because lugnuts may crack and detach, increasing crash risk.

    Product
    TOYOTA — TOYOTA SEQUOIA, TUNDRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V313000·2017-05-11

    Thomas Built Buses Recalling School Buses for Seat Washer Defect

    Daimler Trucks is recalling 2014-2018 Thomas Built Buses Saf-T-Liner EFX and HDX school buses because occupant seats may lack under-rail washers, reducing anchorage strength.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX, SAF-T-LINER EFX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V312000·2017-05-11

    Thomas Built Buses Recalls Minotour School Buses for Seat Defect

    Daimler Trucks North America is recalling 2016-2018 Thomas Built Buses Minotour school buses because occupant seats may lack reinforcement brackets, increasing injury risk in crashes.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17150·2017-05-11

    Carrier and Bryant Heat Pumps Recalled for Fire Hazard

    Carrier and Bryant are recalling about 23,300 heat pumps because capacitors can fail, causing the units to overheat and pose a fire hazard.

    Product
    Carrier Greenspeed™ and Bryant Evolution Extreme™ Heat Pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V314000·2017-05-11

    Thomas Built Buses Recalls Saf-T-Liner HDX Models for Seat Belt Defect

    Daimler Trucks North America is recalling 2013-2018 Thomas Built Saf-T-Liner HDX buses because seat lap belts may be anchored to the seat rather than the bus structure, increasing injury risk in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17149·2017-05-11

    Nature's Truth Recalls Iron Supplements Due to Non-Child-Resistant Packaging

    Nature's Truth is recalling Slow Release Iron 45 mg supplements because the bottles do not meet child-resistant closure requirements. Consumers should keep the product away from children and return it for a refund or replacement.

    Product
    Nature's Truth Slow Release Iron Supplements
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V309000·2017-05-11

    Volkswagen Recalls 2012-2014 Passat Diesel Models for Fire Risk

    Volkswagen is recalling 2012-2014 Passat diesel vehicles because a short heat shield may allow grease to leak and contact hot exhaust parts, increasing fire risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN PASSAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V317000·2017-05-11

    Thomas Built Buses Recalls 2013-2018 Saf-T-Liner HDX School Buses

    Daimler Trucks North America is recalling 2013-2018 Thomas Built Saf-T-Liner HDX school buses because seat lap belts may be anchored to the seat rather than the bus structure.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0690-2017·2017-05-10

    EpiPen Auto-Injectors Recalled for Defective Delivery System

    Meridian Medical Technologies is recalling EpiPen auto-injectors because the delivery system may fail to activate, preventing patients from receiving epinephrine.

    Product
    EPIPEN — EPIPEN (EPINEPHRINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0691-2017·2017-05-10

    EpiPen Jr. Auto-Injectors Recalled for Delivery System Defects

    Meridian Medical Technologies is recalling EpiPen Jr. auto-injectors because the delivery system may fail to activate, preventing patients from receiving epinephrine.

    Product
    EPIPEN — EPIPEN (EPINEPHRINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1929-2017·2017-05-10

    Olympus Endoeye HD II Video Telescopes Recalled for Overheating Tip

    Olympus is recalling 863 Endoeye HD II video telescopes because a damaged temperature sensor can cause the tip to become abnormally hot.

    Product
    Olympus ENDOEYE HD II Video Telescopes Models: WA50040A Endoeye HD II, 10 mm, 0 deg., autoclavable; WA50042A Endoeye HD II, 10 mm, 30 deg., autoclavable; repair cable 10mm 0/30 deg., part number W7100603
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1874-2017·2017-05-10

    Medtronic Recalls Newport HT70 Ventilators Due to Spontaneous Shutdown Risk

    Medtronic is voluntarily recalling Newport HT70 and HT70 Plus ventilators because they may shut down spontaneously without an alarm during normal operation.

    Product
    Newport Medical HT70 and HT70- Plus Ventilators, Rx Only Product Usage: The Newport HT70 family of ventilators is intended to provide continuous or intermittent positive pressure mechanical ventilatory support for the care of individuals who require mechanical ventilation…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2034-2017·2017-05-10

    Sysmex XN Series Hematology Analyzers Recalled for Fire Risk

    Sysmex America Inc is recalling XN-10 and XN-11 hematology analyzers due to a risk of fire caused by misaligned internal protective sheets.

    Product
    Sysmex, Automated Hematology Analyzer XN Series, Sysmex Corporation, 1-5-1 Wakinohama-Kaigandori, Chuo-ku, Kobe 651-0073 Japan
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1899-2017·2017-05-10

    Roche Recalls Accu-Chek Connect App Due to Bolus Advisor Error

    Roche Diabetes Care is recalling specific versions of the Accu-Chek Connect app because a bug in the Bolus Advisor feature may provide incorrect insulin dosing advice.

    Product
    Accu-Chek Connect Diabetes Management App versions 2.0.0, 2.0.1 and 2.1.0 for iOS and Android Product Usage: This is a digital product available for download direct to customers from the Apple App Store and the Google Play Store. The total number of downloads is not…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1924-2017·2017-05-10

    Natus Medical Recalls neoBLUE 2 Phototherapy Lights for Intensity Defect

    Natus Medical is recalling neoBLUE 2 phototherapy lights sold from 2003 to 2008 to prevent the use of replacement boards that allow higher light intensity than originally cleared.

    Product
    Second generation neoBLUE LED Phototherapy Light (neoBLUE 2) sold between 2003 and 2008. Catalog Part Number 010066. Top Assembly Part Numbers: 040906, 040904, 040756, 040758, 040658, 040680. Product Usage: Device is used to provide treatment for neonatal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17E025000·2017-05-10

    Sprague Heavy-Duty Bus Wiper Arms Recalled for Mounting Casting Cracks

    Sprague Devices is recalling Heavy-Duty Bus Pantograph Wiper Arms because the mounting casting may crack, causing the arms to bend or detach and reducing driver visibility.

    Product
    VISIBILITY:WINDSHIELD WIPER/WASHER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1928-2017·2017-05-10

    Dale Medical Stabilock Endotracheal Adhesive Base Recalled for Adhesive Failure

    Dale Medical Products is recalling Stabilock Endotracheal Adhesive Bases because the adhesive faceplate may lose its properties and fail to adhere to the patient's face.

    Product
    Dale Medical Stabilock Endotracheal Adhesive Base Product # 273 The Dale Stabilock Endotracheal Tube Bolder 270 is a 2 piece device consisting of an adhesive base, Dale product number 273, that attaches to the patient's skin and a cushioned neckband with tube channel that…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1903-2017·2017-05-10

    Breg Inc Recalls Sterile Dressings Due to Unsealed Pouches

    Breg Inc is recalling 2,609 units of Dressing Rect L (P/N 02428) because some may have unsealed pouches, rendering them non-sterile.

    Product
    Dressing Rect L, P/N 02428 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy pad and the skin. Sterile dressings are typically applied in a non-sterile environment after post-op and on occasion may be…
    Category
    Medical Device
    Distribution
    Distributed nationwide