The Recall Desk

State

American Samoa product recalls

72,992 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 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9351–9375 of 73017

  • HighNHTSA·24V716000·2024-09-27

    BMW R18 reverse gear control unit seal can let moisture in

    BMW is recalling certain 2021-2024 R18 motorcycles because the seal for the reverse gear control unit may deteriorate, allowing moisture inside and causing the unit to overheat.

    Product
    BMW — BMW R 18
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V713000·2024-09-27

    Royal Enfield motorcycles have insufficient side and rear reflectors

    Royal Enfield is recalling certain 2023 Himalayan, Classic 350, Meteor 350, Hunter 350, Super Meteor 650, Int 650 and Continental GT 650 motorcycles whose side and rear reflectors fail FMVSS 108.

    Product
    ROYAL ENFIELD — ROYAL ENFIELD SUPER METEOR 650, CLASSIC 350, HIMALAYAN, HUNTER 350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V722000·2024-09-27

    Forest River Recalls 2024-2025 Viking and Clipper Trailers for Lighting Defect

    Forest River is recalling 2024-2025 Viking and Clipper travel trailers because side marker lights may not reflect light properly, reducing visibility to other drivers.

    Product
    FOREST RIVER — FOREST RIVER, VIKING TRAVEL TRAILERS CLIPPER CAMPING TRAILER, VIKING
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24E081000·2024-09-27

    EVject Recalls Electric Vehicle Charging Cable Adapters Lacking Thermal Protection

    EVject is recalling Escape Connector NACS v1.0 and v1.1 charging cable adaptors because they lack internal thermal protection, creating a risk of overheating and burn injury.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:CHARGING:CABLE/CORD:ACCESSORY recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V725000·2024-09-27

    Ford stripped chassis gear position indicator may not display properly

    Ford is recalling certain 2024 F-53 and F-59 stripped chassis vehicles because the instrument panel cluster may not properly display the transmission gear position indicator, failing FMVSS 102.

    Product
    FORD — FORD F-59, F-53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V717000·2024-09-26

    Brinkley Model Z safety chains are underrated for the weight rating

    Brinkley RV is recalling certain 2025 Model Z travel trailers because the installed safety chains are underrated for the Gross Vehicle Weight Rating. 40 units are affected.

    Product
    BRINKLEY RV — BRINKLEY RV MODEL Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24377·2024-09-26

    John Deere Compact Utility Tractors Recalled for Brake Failure Hazard

    Deere & Company is recalling about 147,900 John Deere 1023E, 1025R, and 2025R Compact Utility Tractors because the front bell crank in the brake linkage can fail, causing loss of braking and crash risk. Four failures have been reported, including one hospitalization and two impact injuries.

    Product
    John Deere 1023E, 1025R, and 2025R Compact Utility Tractors
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V718000·2024-09-26

    Tesla Cybertruck rearview camera image may be delayed after shifting

    Tesla is recalling certain 2024 Cybertruck vehicles because the rearview camera image may be delayed after shifting into reverse, failing FMVSS 111. 27,185 units affected.

    Product
    TESLA — TESLA CYBERTRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V715000·2024-09-26

    Chrysler Recalls 2024 Ram Promaster BEV for Software Defect

    Chrysler is recalling 2024 Ram Promaster BEV vehicles because incorrect software may cause a loss of drive power, increasing crash risk.

    Product
    RAM — RAM PROMASTER BEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V719000·2024-09-26

    Harley-Davidson Recalls 2018-2019 Softail Motorcycles for Tire Label Error

    Harley-Davidson is recalling 2018-2019 Softail FXBB and FXLR motorcycles because the front tire inflation pressure on the VIN label may be incorrect, potentially leading to tire overloading.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FXBB, FXLR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·24378·2024-09-26

    Liberty Hardware Multi-Grip Tub Safety Bars Recalled for Fall Hazard

    Liberty Hardware is recalling about 174,500 Multi-Grip Tub Safety Bars because plastic grip pads can become dislodged on tapered tubs, making the bars unstable and creating a fall hazard. One minor fall injury has been reported.

    Product
    Multi-Grip Tub Safety Bars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E079000·2024-09-25

    Tenneco Aftermarket Ball Joint Recall for Ford Escape Vehicles

    Tenneco is recalling aftermarket ball joints for 2013-2019 Ford Escape vehicles because they may separate, causing loss of steering control.

    Product
    SUSPENSION:FRONT:CONTROL ARM:LOWER BALL JOINT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1809-2024·2024-09-25

    Bliss Tree Millet Butter Murukku Recalled for Undeclared Sesame and Milk Allergens

    Bliss Tree Millet Butter Murukku products are being recalled due to undeclared sesame and milk allergens. Affected products were distributed to retailers and online customers in multiple states.

    Product
    Bliss Tree Millet Butter Murukku 200g UPC:8906087451631. Packaged in box, 13 boxes per cases. Bliss Tree Millet Butter Murukku 400g UPC:8906087452850. Packaged in pouches, 8 pouches per cases.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V711000·2024-09-25

    BMW and MINI front body structure bolts may not be tightened

    BMW is recalling certain 2023-2024 228i, 228i xDrive and 2025 MINI Countryman S ALL4 vehicles because the bolts connecting the front body structure to the chassis may be loose.

    Product
    BMW — BMW, MINI 228I XDRIVE, 228I, COUNTRYMAN S ALL4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V714000·2024-09-25

    BMW Recalls 2024-2025 Models Due to Steering Spindle Breakage Risk

    BMW is recalling specific 2024-2025 models because the steering spindle may break, increasing steering effort and crash risk. Dealers will replace the joint free of charge.

    Product
    BMW — BMW 540I XDRIVE, I5 EDRIVE40, 760I XDRIVE, 530I XDRIVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3165-2024·2024-09-25

    Philips Azurion X-ray Systems: Cable Hose Carrier Detachment Risk

    Philips recalls Azurion X-ray imaging systems due to potential cable hose carrier detachment from broken plastic or bolts, which may cause parts to fall and create injury risk.

    Product
    System Code Name: 722282 Azurion 7 M20 722281 Azurion 5 M20 722236 Azurion 7 B20 722235 Azurion 7 B12 722234 Azurion 7 M20 722233 Azurion 7 M12 722228 Azurion 5 M20 722227 Azurion 5 M12 722226 Azurion 7 B20 722225 Azurion 7 B12 722224 Azurion 7 M20 722223 Azurion 7 M12 722222 Azu
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3140-2024·2024-09-25

    Alaris EtCO2 Module Model 8300 Recalled Due to Bent Connector

    CareFusion 303, Inc. recalls 180 Alaris EtCO2 Module Model 8300 units with potentially bent female connectors that may prevent device operation, risking delays in infusion and monitoring.

    Product
    Alaris EtCO2 Module Model 8300, a modular infusion pump and monitoring system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3142-2024·2024-09-25

    Alaris Pump Module 8100 Recalled for Bent Connector That May Disable Device

    CareFusion is recalling approximately 192,964 Alaris Pump Module Model 8100 infusion pumps that may have bent female connectors preventing device operation and delaying patient treatment.

    Product
    Alaris Pump Module Model 8100, a modular infusion pump and monitoring system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3180-2024·2024-09-25

    Beckman Coulter Analyzer Recalled for Pneumatic Tubing Defects

    Beckman Coulter is recalling the DxI 9000 Access Immunoassay Analyzer due to undersized pneumatic tubing in the reagent storage module, which can cause air leaks and compressor failures, potentially leading to test errors and delayed results.

    Product
    Beckman Coulter DxI 9000 Access Immunoassay Analyzer, Model Number C21510, RSM Pneumatic Tubing Kit item #2, REF C11137; in vitro diagnostic instrument
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3175-2024·2024-09-25

    Hemodialysis bloodline tubing recalled for improper connector insertion risk

    B. Braun is recalling approximately 4.98 million STREAMLINE FRESENIUS FOR DAVITA hemodialysis bloodline tubes due to risk of improper connector insertion, which could cause blood flow occlusion during dialysis treatment.

    Product
    STREAMLINE FRESENIUS FOR DAVITA-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2000M2095DA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3164-2024·2024-09-25

    Endo Retrieval Pouches Recalled; Tube May Detach During Endoscopic Use

    Endo retrieval pouches are recalled because the tube may detach and fall into the surgical site during use. Approximately 81,241 units distributed in Georgia, Missouri, and Pennsylvania are affected.

    Product
    1. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF TM2001, 3" x 6", sterile; 2. Tech Medical Services Inc. Detachable Endo Retrieval Pouch, REF TM2000, 5" x 7", sterile; 3. Tech Medical Services, Inc. Detachable Endo Retrieval Pouch, REF TM2002, 8" x 10", s
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3163-2024·2024-09-25

    Innovasis spinal fusion devices recalled for implant-inserter interface defect

    Innovasis is recalling TxHA PEEK and TxTiHA IBF intervertebral fusion devices due to interfacing issues between the implant and inserter that may prevent proper placement. The recall affects 568 devices distributed nationwide.

    Product
    TxHA PEEK IBF/TxTiHA IBF System REF BTA-151 i. TxHA The Innovasis TxHA PEEK IBF System is an intervertebral body fusion device intended to stabilize a spinal segment to promote fusion using bone graft, in order to restrict motion and decrease pain. Users of these products ar
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3145-2024·2024-09-25

    GE Healthcare ViewPoint Imaging System Recall for Data Vulnerability

    GE Healthcare is recalling three ViewPoint imaging systems due to a software vulnerability in Mirth Connect that could allow unauthorized access and manipulation of patient data.

    Product
    ViewPoint; system, imaging processing, radiological
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3173-2024·2024-09-25

    Hemodialysis Bloodline Tubing Recall Over Incomplete Connector Insertion Risk

    B Braun is recalling SL BLOODLINE FOR FMC 2008 SERIES hemodialysis tubing nationwide due to incomplete connector insertion that may cause blood flow restrictions during treatment.

    Product
    SL BLOODLINE FOR FMC 2008 SERIES-Tubing to be used to transfer blood between a patient and a haemodialyser during haemodialysis. Model/Catalog Number: SL-2000M2095
    Category
    Medical Device
    Distribution
    Distributed nationwide