The Recall Desk

State

American Samoa product recalls

73,570 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 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27001–27025 of 73595

  • SevereNHTSA·20V689000·2020-11-06

    Autocar Xpeditor and Legend suspension bolts may fail and disconnect

    Autocar is recalling 2020-2021 Xpeditor and Legend vehicles because transverse torque rod mounting bolts may not be properly tightened. If bolts fail and disconnect, vehicles could lose suspension control, increasing crash risk.

    Product
    AUTOCAR — AUTOCAR LEGEND, XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E083000·2020-11-06

    First Light Recalls Illuminated School Bus Stop Signs Due to Seal Defect

    First Light Safety Products is recalling illuminated school bus stop signs sold for specific bus models between April and October 2020. A defective weather seal may allow contaminants to enter, potentially causing electrical shorts and rendering the signs inoperable.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V687000·2020-11-06

    2020-2021 Autocar Xpeditor ground cable may cause engine stall

    Certain 2020-2021 Autocar Xpeditor vehicles with X12N engines may have a ground cable that is too short and could fail, causing engine stall without restart capability. Autocar will replace the cable free of charge.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V683000·2020-11-05

    Land Rover Recalls 2020 Models Due to Electrical Fire Risk

    Jaguar Land Rover is recalling 2020 Discovery Sport and Range Rover Evoque MHEV vehicles because an electrical short-circuit could cause a fire.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE, DISCOVERY SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V686000·2020-11-05

    Freightliner Recalls Econic SD Trucks for Electrical Fire Risk

    Daimler Trucks North America is recalling 2019-2021 Freightliner Econic SD vehicles because damaged electrical cables may cause a fire or engine stall.

    Product
    FREIGHTLINER — FREIGHTLINER ECONIC SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V684000·2020-11-05

    2020 Chevrolet Silverado 1500 Overcured Tire Recall May Increase Crash Risk

    General Motors is recalling certain 2020 Chevrolet Silverado 1500 vehicles with overcured Continental tires that may experience sudden air loss or tread separation, increasing crash risk.

    Product
    GMC — GMC, CHEVROLET, BUICK ACADIA, TRAVERSE, ENCLAVE, XT5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V685000·2020-11-05

    Nissan Recalls 2020 Altima Vehicles Due to Over-Cured Tires

    Nissan is recalling 2,214 2020 Altima S vehicles because specific Continental tires may be over-cured, increasing the risk of a crash.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V682000·2020-11-04

    Toyota and Lexus Recall Vehicles for Fuel Pump Failure Risk

    Toyota is recalling over 1.5 million vehicles because a fuel pump defect may cause the engine to stall while driving, increasing crash risk.

    Product
    LEXUS — LEXUS, TOYOTA RX350, LC500, LS500, LS HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0290-2021·2020-11-04

    GORE TAG CONFORMABLE Thoracic Stent Graft Recall for Deployment Issue

    W L Gore is recalling GORE TAG CONFORMABLE Thoracic Stent Grafts because a secondary deployment fiber attachment prevented completion of deployment via the access hatch.

    Product
    GORE TAG CONFORMABLE Thoracic Stent Graft with ACTIVE CONTROL System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0054-2021·2020-11-04

    Bausch Health Recalls Subpotent Hydrocortisone Butyrate Cream

    Bausch Health is recalling 35,424 tubes of Hydrocortisone butyrate Cream, 0.1%, because the product was found to be subpotent.

    Product
    Hydrocortisone butyrate Cream, 0.1%, 15-gram tubes, Rx Only, Manufactured for Oceanside Pharmaceuticals a division of Valeant Pharmaceuticals North America LLC Bridgewater, NJ 08807 USA, By: Ferndale Laboratories, Inc. Ferndale, MI 48220, NDC 68682-270-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V681000·2020-11-04

    Volvo Recalls S60 and S80 Vehicles Due to Air Bag Inflator Defect

    Volvo is recalling 2001-2003 S60 and S80 vehicles because the driver-side air bag inflator may rupture, sending metal fragments into the vehicle.

    Product
    VOLVO — VOLVO S60, S80
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V678000·2020-11-04

    Certain 2020-2021 BMW X5, X6, X7 models: suspension weld separation

    Certain 2020-2021 BMW X5, X6, X7, and related models have a front axle support weld that may separate, potentially affecting vehicle handling and control and increasing crash risk.

    Product
    BMW — BMW X6 M, X5, X6, X7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0286-2021·2020-11-04

    Boston Scientific Recalls Hurricane RX Biliary Balloon Catheters Due to Detachment Risk

    Boston Scientific is recalling Hurricane RX Biliary Balloon Dilatation Catheters because the black sheath may detach from the shaft. The recall covers 15,062 units in the US and 12,930 internationally.

    Product
    Hurricane RX Biliary Balloon Dilatation Catheter Catalog REF No. M00545890; M00545900; M00545910; M00545920; M00545930; M00545940; M00545950; M00545960 The device is a double lumen catheter with a balloon mounted at the distal tip. Dilatation balloon catheters are used to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0285-2021·2020-11-04

    Philips Recalls Sterilizable Defibrillator Paddles Due to Undetected Failure Mode

    Philips is recalling 2,202 sterilizable defibrillator paddles because standard periodic checks may fail to detect a specific failure mode in switchless internal models.

    Product
    Philips Sterilizable Defibrillator Paddles, Switchless Internal Paddles, Model Numbers M1741A, M1742A, M1743A, M1744A - Product Usage: used in pairs to transmit a controlled electrical shock from an external defibrillator directly to the exposed heart muscle of a post-pubescent…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0309-2021·2020-11-04

    Battelle Recalls Critical Care Decontamination System N95 Respirators

    Battelle Memorial Institute is recalling 898 N95 respirators decontaminated by its Critical Care Decontamination System. The recall is due to a failure to maintain required condensation levels during the decontamination cycle.

    Product
    Critical Care Decontamination System (CCDS) Compatible N95 respirators - Product Usage: Used in decontaminating compatible N95 respirators2 for multiple-user3 reuse by healthcare personnel (HCP)4 to prevent exposure to pathogenic biological airborne particulates when there are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21018·2020-11-04

    Rogue Home Timers Recalled by CPSC Due to Fire Hazard

    Coulter Ventures is recalling Rogue Home Timers because the lithium-ion battery can overheat and burn, posing a fire hazard.

    Product
    Rogue Home Timers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0292-2021·2020-11-04

    Pentax 9372HD Digital Capture Software Recall for Patient Data Error

    Pentax of America Inc. is recalling 39 units of the 9372HD Digital Capture system due to a software issue that may copy exam videos to the wrong patient.

    Product
    9372HD Digital Capture (ver. 1.1.0 + w/ 9263 endoPortal),
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0293-2021·2020-11-04

    Pentax 9310HD Digital Video Capture Module Recalled for Software Error

    Pentax of America Inc is recalling 39 units of the 9310HD Digital Video Capture Module due to a software issue that may copy patient exam videos to the wrong record.

    Product
    9310HD Digital Video Capture Module with software version 3.4.0 or higher configured with 9263 endoPortal
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0299-2021·2020-11-04

    RTI Surgical Recalls Streamline MIS Navigation System Taps Due to Binding

    RTI Surgical is recalling 420 units of Streamline MIS Navigation System Taps because they have experienced binding with other devices.

    Product
    Streamline MIS Navigation System Taps, Catalog Nos. 04-CANNDRILL-MDN 04-CANNTAP-40-MDN 04-CANNTAP-45-MDN 04-CANNTAP-55-MDN 04-CANNTAP-65-MDN 04-CANNTAP-75-MDN 04-CANNTAP-85-MDN 04-CTAP-TT-65-MDN 04-S-FINDER-MDN 05-SCREWINS-CL-MDN 05-SIMPDRIVER-MDN Product Usage…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21021·2020-11-04

    Target Recalls Cat & Jack Toddler Boots Due to Choking Hazard

    Target is recalling approximately 122,500 Cat & Jack toddler boots because the toggle can detach, posing a choking hazard to children.

    Product
    Cat & Jack "Himani" and "Jaren" Toddler Boots
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0291-2021·2020-11-04

    GORE TAG Stent Graft Recalled Due to Delivery Catheter Removal Issue

    W.L. Gore is recalling GORE TAG stent grafts because the delivery catheter could not be withdrawn after implantation.

    Product
    GORE TAG Conformable Thoracic Stent Graft with ACTIVE CONTROL System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0306-2021·2020-11-04

    GE Healthcare Recalls CT Scanners Due to Potential Image Artifacts

    GE Healthcare is recalling 64 CT scanners worldwide because incorrect settings may cause smudge artifacts that could be mistaken for pathology.

    Product
    Revolution Apex, Revolution CT with Apex Edition, Model 5995000-5 - Product Usage: The system is intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide