The Recall Desk

State

American Samoa product recalls

73,495 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 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24326–24350 of 73520

  • SevereNHTSA·21V501000·2021-07-01

    Mac Trailer Recalls 2017-2020 Dump Trailers Due to Steering Arm Defect

    Mac Trailer Mfg. is recalling 2017-2020 dump trailers because the steering arm may detach, potentially causing loss of steering control or road hazards.

    Product
    MAC TRAILERS — MAC TRAILERS DUMP TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V505000·2021-07-01

    Bwise Recalls 2021-2022 Trailers Due to Coupler Defect

    Bwise is recalling 2021-2022 Utility, Car Hauler, Dump, Tilt, and Equipment trailers because a coupler defect may cause the trailer to uncouple, increasing crash risk.

    Product
    BWISE — BWISE DUMP TRAILER, EQUIPMENT TRAILER, UTILITY TRAILER, TILT TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V496000·2021-07-01

    GM Recalls 2017-2019 Chevrolet and GMC Trucks for Fire Risk

    General Motors is recalling 2017-2019 Chevrolet Silverado and GMC Sierra trucks with Duramax diesel engines due to an electrical short-circuit risk in the engine-block heater that could cause a fire.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 2500, SIERRA 3500, SIERRA 2500, SILVERADO 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V500000·2021-07-01

    Jaguar Recalls 2018 F-Type for Front Passenger Air Bag Defect

    Jaguar is recalling one 2018 F-Type vehicle because the instrument panel may interfere with the front passenger air bag, potentially causing it to tear during deployment.

    Product
    JAGUAR — JAGUAR F-TYPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V494000·2021-07-01

    Mazda Recalls 2004-2007 Mazda3 for Air Bag Cover Shattering Risk

    Mazda is recalling 2004-2007 Mazda3 vehicles because the steering wheel air bag cover may shatter during deployment, projecting plastic fragments into the vehicle.

    Product
    MAZDA — MAZDA MAZDA3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V495000·2021-07-01

    2021 Chevrolet Silverado 1500 driver air bag may fail to deploy properly

    General Motors is recalling certain 2021 Chevrolet Silverado 1500 vehicles due to a defect in the driver's side frontal air bag module. Missing metal tabs may prevent proper air bag deployment in a crash, increasing the risk of injury.

    Product
    CHEVROLET — CHEVROLET SILVERADO 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V499000·2021-07-01

    Land Rover Recalls 2021 Defender 90 Vehicles for Front Seat Track Defect

    Jaguar Land Rover is recalling 2021 Defender 90 vehicles because a front seat track bracket may deform, preventing the seat from locking and increasing injury risk in a crash.

    Product
    LAND ROVER — LAND ROVER DEFENDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V497000·2021-07-01

    2021 GMC Canyon Vehicles Recalled for Incorrect Tire Load Capacity Label

    General Motors is recalling 7,199 2021 GMC Canyon vehicles because the tire and loading information placard lists load capacity 51 pounds higher than intended, increasing the risk of vehicle overload and crashes.

    Product
    GMC — GMC CANYON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21759·2021-07-01

    The Best Damn Liquids Liquid Nicotine Recalled for Non-Child-Resistant Packaging

    TBD Liquids is recalling approximately 1,000 units of The Best Damn Liquids branded liquid nicotine because the packaging is not child-resistant as required by law. Liquid nicotine is toxic if swallowed or absorbed through skin or eyes.

    Product
    The Best Damn Liquids branded liquid nicotine
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V502000·2021-07-01

    2021 Aprilia Tuono 660 and RS 660 recalled for engine crankshaft defect

    Aprilia is recalling 2021 Tuono 660 and RS 660 motorcycles because the engine crankshaft connecting rod may break due to improper heat-treatment, risking sudden engine stall and crash.

    Product
    APRILIA — APRILIA TUONO 660, RS 660
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·21758·2021-07-01

    Rejuvenation Deep Frame Mirrors Recalled for Laceration Hazard

    Rejuvenation is recalling about 3,325 Deep Frame Mirrors because the adhesive securing the mirror glass can fail, causing the glass to detach and fall out of the frame. Rejuvenation has received 18 reports of glass detaching, though no injuries have been reported.

    Product
    Deep Frame Mirrors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0634-2021·2021-06-30

    PremierZEN Platinum 8000 Capsules Recalled for Undeclared Drug Ingredients

    PremierZEN Platinum 8000 capsules, distributed nationwide, are being recalled because the product contains undeclared pharmaceutical ingredients (Sildenafil and Tadalafil) and was marketed without FDA approval.

    Product
    PremierZEN Platinum 8000 capsule, 1-count blister card (UPC 7 28175 42185 6), packaged in 12 cards per box (UPC 7 28175 42183 2), Distributed by: New Premier Group, Los Angeles, CA 90006
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0633-2021·2021-06-30

    PremierZEN Gold 7000 Capsule Recalled for Undisclosed Drug Contamination

    PremierZEN Gold 7000 capsules are recalled nationwide because the product contains undisclosed pharmaceutical ingredients Sildenafil and Tadalafil and was marketed without FDA approval.

    Product
    PremierZEN Gold 7000 capsule, 1-count blister card, packaged in 12 cards per box (UPC 7 28175 42183 2), Distributed by: New Premier Group, Los Angeles, CA 90006
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0635-2021·2021-06-30

    maXXzen Platinum 12000 Capsule Recalled for Undisclosed Drug Contaminants

    The FDA is recalling maXXzen Platinum 12000 capsules distributed nationwide because the product was marketed without an approved application and contains undisclosed pharmaceutical ingredients (Sildenafil and Tadalafil).

    Product
    maXXzen Platinum 12000 capsule, 1-count blister card (UPC 7 18122 04072 8), Distributed by: Maxx Inc, Los Angeles, CA 90028
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1863-2021·2021-06-30

    Nitric Oxide Delivery System Dosing Deficiency During Console Transitions

    GENOSYL DS Nitric Oxide Delivery System is recalled for delivering below-intended doses during transitions between primary and backup consoles following a software update.

    Product
    GENOSYL DS; Nitric Oxide Delivery System Combination Product NDA202860
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0688-2021·2021-06-30

    Clio Coconut Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Clio Coconut Less Sugar Yogurt Bars (45g and 50g 10-packs) distributed nationwide due to possible metal fragments in the product.

    Product
    Clio Coconut Less Sugar Yogurt Bars wrapped in a Chocolate Coating 45g x 10 Clio Retail 10-pack and 50g x 10 Clio Retail 10-pack, UPC codes: 854021008237 and 854021008046
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1934-2021·2021-06-30

    Dexcom G6 Sensor 3-Pack Recalled for Temperature-Related Measurement Errors

    Cardinal Health is recalling 2,357 kits of Dexcom G6 Sensor 3-Pack due to temperature exposure during shipping that may cause inaccurate glucose readings. Affected units were distributed in Florida, Georgia, and South Carolina.

    Product
    DEXCOM G6 SENSOR 3 PACK Item Number: 5447552
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1930-2021·2021-06-30

    FREESTYLE LIBRE 14 DAY glucose monitoring system recalled for temperature exposure

    Cardinal Health is recalling 8,959 glucose monitoring kits due to temperature exposure during shipping that may result in inaccurate readings. Affected devices were distributed nationwide.

    Product
    FREESTYLE LIBRE 14 DAY GLUCOSE MONITORING SYSTEM. Item Number: 5479084
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1931-2021·2021-06-30

    FreeStyle Libre 2 Glucose Monitoring System Recalled for Inaccurate Results

    Cardinal Health is recalling FreeStyle Libre 2 glucose monitoring systems shipped between February and March 2021 due to temperature exposure during shipment that may cause inaccurate readings.

    Product
    FREESTYLE LIBRE 2 GLUCOSE MONITORING SYSTEM: Item number: 5658877
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0694-2021·2021-06-30

    Clio Peanut Butter Greek Yogurt Bars Recalled for Possible Metal Fragments

    Clio LLC is recalling Peanut Butter Greek Yogurt Bars due to the possible presence of metal fragments. The affected product was distributed nationwide with best-buy dates between March 7, 2021 and June 20, 2021.

    Product
    Clio Peanut Butter Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC code: 854021008039
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1944-2021·2021-06-30

    FilmArray Pneumonia Panel diagnostic test kits recalled for false results

    BioFire Diagnostics is recalling 9 FilmArray Pneumonia Panel test kits due to manufacturing defects causing false positive and negative test results, as well as control failures.

    Product
    FilmArray Pneumonia Panel (Penumo) REF RFIT-ASY-0144
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21156·2021-06-30

    Children's Nightgowns Recalled for Flammability Standard Violation

    Auranso Official children's nightgowns sold on Amazon fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries. About 8,000 units distributed January–June 2021 are affected.

    Product
    Children's Nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1939-2021·2021-06-30

    OneTouch Delica Lancets Recalled Due to Temperature Exposure During Shipping

    Cardinal Health is recalling OneTouch Delica Lancets (100-count boxes) after devices were exposed to freezing temperatures during shipping, which may affect blood glucose test accuracy. No injuries have been reported.

    Product
    ONETOUCH DELICA LANCETS 30G 100 COUNT Item Number: 5541610
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0687-2021·2021-06-30

    Clio Coconut Greek Yogurt Bars recalled for possible metal fragments

    Clio LLC is recalling Clio Coconut Greek Yogurt Bars in 50g x 10-pack format due to the possible presence of metal fragments. The product was distributed nationwide.

    Product
    Clio Coconut Greek Yogurt Bars wrapped in a Chocolate Coating 50g x 10 Clio Retail 10-pack, UPC: 854021008046
    Category
    Food
    Distribution
    Distributed nationwide