The Recall Desk

State

American Samoa product recalls

73,106 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 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

13201–13225 of 73131

  • HighNHTSA·23V880000·2023-12-21

    Mercedes-Benz vehicles recalled for fuel pump failure affecting drive power

    Mercedes-Benz is recalling 2021–2024 vehicles due to fuel pump failures that may cause loss of drive power, increasing crash risk. Dealers will provide free replacement.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH AMG GLE53, GLE 580 4MATIC, GLS 450 4MATIC, GLS 580 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24066·2023-12-21

    FeraDyne Outdoors Recalls Rhino Tree Stands Due to Fall Hazard

    FeraDyne Outdoors is recalling about 50,000 Rhino Tree Stands because the safety harness stitching can rip, creating a fall hazard. No injuries have been reported.

    Product
    Rhino Tree Stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V869000·2023-12-21

    2024 Chevrolet Equinox door strikers may fracture and open unexpectedly

    General Motors is recalling certain 2024 Chevrolet Equinox and related models because door strikers may fracture, potentially causing doors to open unexpectedly while driving.

    Product
    CHEVROLET — CHEVROLET, GMC BLAZER, EQUINOX, TERRAIN, BLAZER EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24737·2023-12-21

    Litti City and Litti Pritti Dress-Up Playsets and Prextex Slime Eggs Recalled for Phthalate and Lead Violations

    Litti City Premier Doctor and Teacher Purse playsets, Litti Pritti Stylist Handbag set, and Prextex Slime Eggs are recalled for containing phthalates and lead exceeding federal safety standards. No injuries have been reported.

    Product
    Litti City Premier Doctor Playset and Teacher Purse Set, Litti Pritti Stylist Handbag Set, and Prextex Slime Eggs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V881000·2023-12-21

    2022-2023 Mercedes-Benz Metris Fuel Pump May Fail Unexpectedly

    The fuel pumps in certain 2022-2023 Mercedes-Benz Metris vehicles may shut down unexpectedly, causing loss of drive power and increasing the risk of a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24067·2023-12-21

    Klein Tools and Blackfire Portable Power Stations Recalled for Fire and Burn Hazards

    Klein Tools and Blackfire portable rechargeable power stations are being recalled because their internal inverter boards can overheat, creating fire and burn hazards. Consumers should stop using the units and return them to their original point of purchase.

    Product
    Portable Rechargeable Power Stations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24732·2023-12-21

    Pella Architect Series Casement Windows Recalled for Detachment Injury Hazard

    Pella Corporation is recalling approximately 12,000 Architect Series Casement Windows because the window sash can detach from the frame and fall, creating an injury risk. The company has received one report of detachment but no injuries have been reported.

    Product
    Pella Architect Series Casement Windows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V879000·2023-12-21

    Daimler Recalls 2023-2024 Electric Transit Buses Due to Inverter Cable Issue

    Daimler Trucks North America is recalling 26 electric transit buses because a high-voltage inverter cable may not be secured properly, potentially causing a loss of drive power.

    Product
    FCCC — FCCC, THOMAS BUILT BUSES MT50E, SAF-T-LINER C2 JOULEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V882000·2023-12-21

    2024 Nissan Altima Recall for Potential Steering Bolt Loosening

    Nissan is recalling approximately 5 certain 2024 Altima vehicles because bolts connecting the electronic power steering unit to the steering rack may loosen, potentially causing loss of steering control or lock-up. Dealers will replace the steering gear assembly at no cost.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V871000·2023-12-21

    2023 Land Rover Range Rover Sport Exterior Lights May Fail

    Moisture may accumulate in the right-side tailgate and lights of certain 2023 Land Rover Range Rover Sport vehicles, causing exterior lights to fail and reducing visibility.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·24068·2023-12-21

    TJX Foldable Wood and Rope Bistro Set Chairs Recall Due to Fall Hazard

    TJX is recalling about 29,000 foldable wood and rope bistro set chairs because the wooden frame can break or collapse when occupied, creating a fall hazard. The company has received eight reports of frame breakage, including six reports of minor injuries such as bruising and ankle strain.

    Product
    Foldable wood and rope bistro set chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0548-2024·2023-12-20

    CereLink ICP Extension Cable Recalled for Out of Range Readings

    Integra LifeSciences is recalling CereLink ICP Extension Cables due to a design defect causing out of range readings. The Class I recall affects 4,941 units distributed nationwide and internationally.

    Product
    CereLink ICP Extension Cable (Extension Cable), Model No. 826845 Used with Codman CereLink Intracranial Pressure (ICP) Monitor, Model No. 826820/826820P. Cable is also provided with monitor as part of the same SKU.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0543-2024·2023-12-20

    Medical Diagnostic System Recall Due to Software-Related System Freezes and Delayed Results

    Ortho-Clinical Diagnostics is recalling the VITROS 3600 Immunodiagnostic System due to software issues causing system freezes and delayed test result reporting. The delays could affect patient care when rapid results are critical.

    Product
    VITROS 3600 Immunodiagnostic System Product Code 6802783 and Refurbished Product Code 6802914 Running Software Version 3.8.0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0520-2024·2023-12-20

    Medical Device Recall: Para-Pak Zn-PVA Stool Collection Vials for Leakage Risk

    Meridian Bioscience is recalling Para-Pak Zn-PVA stool specimen collection vials due to a manufacturing defect that may cause leakage and risk exposure to biological hazards.

    Product
    Para-Pak Zn-PVA/10% Formalin-for the routine collection, transportation, preservation, and examination of stool specimens for intestinal parasites Catalog Number: 301012
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0528-2024·2023-12-20

    Sterile PVP Medical Solution Recalled for Non-Sterile Contents

    Medline Industries is recalling 700 units of Sterile PVP solution because the labeling claims sterility but the contents are non-sterile. The affected products were distributed nationwide in eight states.

    Product
    STERILE PVP, REF DYNDA1649
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0519-2024·2023-12-20

    Para-Pak Clean Vial Stool Collection Kits Recalled for Manufacturing Defect

    Meridian Bioscience is recalling Para-Pak Clean Vials used for stool specimen collection due to a manufacturing defect that increases leakage risk and may expose users to biological hazards.

    Product
    Para-Pak Clean Vial-For the collection, transportation, preservation, and examination of stool specimens containing intestinal parasites Catalog Number: 900312
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V864000·2023-12-20

    2022-2023 Toyota Corolla Cross air bag deployment defect recall

    Toyota is recalling 2022-2023 Corolla Cross vehicles where instrument panel defects may prevent the front-passenger air bag from deploying in a crash. Dealers will replace the panel at no cost.

    Product
    TOYOTA — TOYOTA COROLLA CROSS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0527-2024·2023-12-20

    Sterile Prep Stick Recall: Non-Sterile Contents Despite Sterile Labeling

    Medline Industries is recalling sterile prep sticks (REF DYNDA1134) labeled as sterile that contain non-sterile solution, posing infection risk in medical procedures.

    Product
    STERILE STERILE PREP STICK, REF DYNDA1134
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V865000·2023-12-20

    Toyota and Lexus vehicles recalled for air bag sensor short circuit defect

    Toyota and Lexus are recalling certain 2020-2022 vehicles with a faulty Occupant Classification System sensor that may prevent the front passenger air bag from deploying in a crash, increasing injury risk.

    Product
    LEXUS — LEXUS, TOYOTA ES, CAMRY HYBRID, AVALON, ES HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0523-2024·2023-12-20

    Collision Sensor Malfunction in Siemens ARTIS Icono Fluoroscopic X-Ray System

    The ARTIS icono fluoroscopic x-ray system may falsely detect collisions for up to 30 minutes after startup, requiring manual override with reduced safety protection and limiting diagnostic use.

    Product
    ARTIS icono (ceiling configuration), Fluoroscopic x-ray system; Model no. 11328100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0551-2024·2023-12-20

    Medical imaging software incorrectly displays patient studies to wrong patients

    Change Healthcare's Stratus Imaging PACS software can incorrectly associate patient imaging studies with the wrong patients. Approximately 454 affected units have been distributed nationwide.

    Product
    Change Healthcare Stratus Imaging PACS 1.4 and Stratus Imaging Share 1.4, a component of Stratus Imaging PACS.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0531-2024·2023-12-20

    Povidone Solution Labeled Sterile Despite Non-Sterile Contents

    Medline Industries recalls 300 units of Sterile Povidone (REF DYNDA2061) after discovering the solution inside foil sachets is non-sterile despite sterile labeling. Affected lots are distributed across eight states.

    Product
    STERILE POVIDONE, REF DYNDA2061
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V867000·2023-12-20

    Audi E-Tron Battery Modules May Overheat Creating Fire Risk

    Audi is recalling 2019-2022 E-Tron vehicles because high-voltage battery modules may overheat and increase fire risk. Dealers will install diagnostic software and replace affected modules at no cost.

    Product
    AUDI — AUDI E-TRON
    Category
    Vehicle
    Distribution
    Distributed nationwide