The Recall Desk

State

American Samoa product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37001–37025 of 73766

  • SevereNHTSA·18V621000·2018-09-14

    Mitsubishi Recalls Outlander Models Due to Safety System Software Defect

    Mitsubishi is recalling 2017-2018 Outlander, Outlander Sport, Eclipse Cross, and Outlander PHEV vehicles because incorrect software may prevent safety systems like automatic emergency braking from functioning.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER, OUTLANDER SPORT, ECLIPSE CROSS, OUTLANDER PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V635000·2018-09-14

    Alfa Romeo Stelvio Recall: Engine Cooling Hose Defect

    Chrysler is recalling 2018-2019 Alfa Romeo Stelvio Quadrifoglio vehicles because an engine cooling hose may leak coolant, causing overheating and stalling.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V633000·2018-09-14

    Cruiser RV Recalls 2019 Travel Trailers Due to Axle Bearing Defect

    Cruiser RV is recalling 2019 travel trailers because missing inner bearing races may cause hub failure and increase crash risk.

    Product
    CRUISER RV — CRUISER RV RADIANCE ULTRA LITE, MPG, FUN FINDER EXTREME LITE, SHADOW CRUISER ULTRA LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V632000·2018-09-14

    Bentley Recalls 2018 Mulsanne and Bentayga for Rearview Camera Issues

    Bentley is recalling 2018 Mulsanne and Bentayga vehicles because the rearview camera display may be obstructed or delayed, increasing crash risk when reversing.

    Product
    BENTLEY — BENTLEY BENTAYGA, MULSANNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V620000·2018-09-14

    Mitsubishi Recalls Outlander and Eclipse Cross Models for Braking Software Defect

    Mitsubishi is recalling certain 2017-2019 Outlander, Outlander Sport, Eclipse Cross, and Outlander PHEV vehicles because faulty software may cause the Forward Collision Mitigation system to brake for too long, increasing the risk of a rear-end collision.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER, OUTLANDER SPORT, ECLIPSE CROSS, OUTLANDER PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V630000·2018-09-13

    Honda Recalls 2018 CRF250L Motorcycles Due to Wiring Harness Defect

    Honda is recalling 2018 CRF250L motorcycles because an improperly installed wiring harness may damage safety components like lights and the horn, increasing crash risk.

    Product
    HONDA — HONDA CRF250L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V628000·2018-09-13

    Forest River Recalls 2019 East to West Travel Trailers Due to Axle Issue

    Forest River is recalling 2019 East to West travel trailers because incorrect axle shackles may allow tires to contact the wheel well, risking tire failure and loss of control.

    Product
    FOREST RIVER — FOREST RIVER EAST TO WEST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V624000·2018-09-13

    Forest River Recalls 2019 Travel Trailers Due to Axle Bearing Defect

    Forest River is recalling 2019 travel trailers because missing inner bearing races may cause hub overheating or separation, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN XLR, VIBE, SIERRA, SHASTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V626000·2018-09-13

    Subaru Recalls 2010-2014 Legacy and Outback for Parking Brake Defect

    Subaru is recalling 2010-2014 Legacy and Outback vehicles with manual transmissions because the electronic parking brake may fail to engage, increasing the risk of a crash.

    Product
    SUBARU — SUBARU OUTBACK, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V622000·2018-09-13

    KME Fire Trucks Recalled for Brake Light Wiring Defect

    KME is recalling 111 fire trucks because brake lights may illuminate without the pedal being pressed, potentially confusing other drivers.

    Product
    KME — KME COMMERCIAL PUMPER, COMMERCIAL TANKER, COMMERCIAL WILDLAND, PREDATOR PANTHER TANKER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V623000·2018-09-13

    Forest River Berkshire Motorhomes Recalled for Door Latch Defect

    Forest River is recalling 2019 Berkshire motorhomes because improperly adjusted door latch rods may allow the entry door to open while the vehicle is moving.

    Product
    FOREST RIVER — FOREST RIVER BERKSHIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V625000·2018-09-13

    Land Rover Recalls 2018 Models for Silent Automatic Emergency Braking Failure

    Jaguar Land Rover is recalling 2018 Discovery, Range Rover, and Range Rover Sport vehicles because the Automatic Emergency Braking system may disable without warning, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER DISCOVERY, RANGE ROVER SPORT, RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V617000·2018-09-12

    Altec Recalls 2018 Cranes, Derricks, and Aerial Devices Due to Fastener Defect

    Altec Industries is recalling 2018 cranes, digger derricks, and aerial devices because overtightened fasteners may break, potentially causing the platform to separate from the vehicle.

    Product
    ALTEC — ALTEC DIGGER DERRICK, CRANE, AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1173-2018·2018-09-12

    AvKARE Valsartan and Hydrochlorothiazide Tablets Recalled for Carcinogen Impurity

    AvKARE is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    AvKARE Valsartan and Hydrochlorothiazide 80 mg/12.5 mg tablets, 90-count bottle, Rx Only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478, NDC 42291-884-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1176-2018·2018-09-12

    AvKARE Valsartan and Hydrochlorothiazide Tablets Recalled for Carcinogen Impurity

    AvKARE is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    AvKARE Valsartan and Hydrochlorothiazide 320 mg/12.5 mg tablets, 90-count bottle, Rx Only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478, NDC 42291-886-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2990-2018·2018-09-12

    GE Vivid E7 Ultrasound System Recalled for Power Cord Shock Risk

    GE Medical Systems is recalling Vivid E7 ultrasound systems because the power cord may break and expose electrical conductors, creating a risk of electric shock.

    Product
    GE Vivid E7 ultrasound system Product Usage: Vivid E7 is a general-purpose ultrasound system, specialized for use in cardiac imaging. It is intended for use by, or under the direction of a qualified physician for ultrasound imaging and analysis of Fetal/Obstetrics; Abdominal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1174-2018·2018-09-12

    AvKARE Valsartan and Hydrochlorothiazide Tablets Recalled for Carcinogen Impurity

    AvKARE is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    AvKARE Valsartan and Hydrochlorothiazide 160 mg/12.5 mg tablets, 90-count bottle, Rx Only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478, NDC 42291-885-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1177-2018·2018-09-12

    AvKARE Valsartan and Hydrochlorothiazide Tablets Recalled for Carcinogen Impurity

    AvKARE is recalling Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    AvKARE Valsartan and Hydrochlorothiazide 320 mg/25 mg tablets 90-count bottle, Rx Only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478, NDC 42291-888-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1175-2018·2018-09-12

    AvKARE Valsartan and Hydrochlorothiazide Tablets Recalled for Carcinogen Impurity

    AvKARE is recalling specific lots of Valsartan and Hydrochlorothiazide tablets because a carcinogen impurity was detected in the active pharmaceutical ingredient.

    Product
    AvKARE Valsartan and Hydrochlorothiazide 160 mg/25 mg tablets, 90-count bottle, Rx Only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478, NDC 42291-887-90
    Category
    Drug
    Distribution
    Distributed nationwide