The Recall Desk

State

American Samoa product recalls

73,509 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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25651–25675 of 73534

  • HighNHTSA·21V149000·2021-03-09

    Autocar Recalls 2020-2021 Legend Vehicles for Steering Column Defect

    Autocar is recalling 2020-2021 Legend vehicles because the steering column tilt control cable may contact the steering shaft, potentially causing it to bind and increasing steering effort.

    Product
    AUTOCAR — AUTOCAR LEGEND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E017000·2021-03-08

    WP Dynamics Lift Kit Recall for Improperly Treated Bolts

    WP Dynamics is recalling ReadyLIFT Lift Kits for certain Ford and Dodge trucks because improperly heat-treated bolts may break, risking suspension separation and loss of vehicle control.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E016000·2021-03-08

    MEKRA Recalls Exterior Rearview Mirror Housings for Detachment Risk

    MEKRA Lang North America is recalling specific exterior rearview mirror housings because the glass may detach, reducing visibility or creating road hazards.

    Product
    VISIBILITY:REARVIEW MIRRORS/DEVICES:EXTERIOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V142000·2021-03-05

    Volkswagen Recalls 2018-2019 Atlas Vehicles Due to Tire Defect

    Volkswagen is recalling 2018-2019 Atlas vehicles equipped with specific Continental tires that may have been over-cured during production, posing a risk of sudden air loss or loss of vehicle control.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V140000·2021-03-05

    Ford Recalls 2021 Mustang Mach-E for Loose Front Subframe Bolts

    Ford is recalling 2021 Mustang Mach-E vehicles because front subframe bolts may not have been tightened properly, which could reduce crash performance and increase injury risk.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V143000·2021-03-05

    Custom Truck Recalls Two Vehicles for Excessively Bright LED Lights

    Custom Truck is recalling one 2016 Ford F-550 and one 2018 International 4000 because their LED lights are too bright, potentially blinding other drivers.

    Product
    CUSTOM TRUCK & BODY WORKS — CUSTOM TRUCK & BODY WORKS FORD F-550, INTERNATIONAL 4000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V141000·2021-03-05

    2021 Forest River Cardinal and Wildcat furnace flue misalignment recall

    Forest River is recalling certain 2021 Cardinal and Wildcat recreational vehicles due to furnace flue misalignment. Furnace exhaust may leak into the living space, creating a risk of injury or death.

    Product
    FOREST RIVER — FOREST RIVER WILDCAT, CARDINAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V138000·2021-03-04

    2020-2021 Nissan Altima tie rod fastener defect may cause steering loss

    Nissan is recalling certain 2020-2021 Altima vehicles because the tie rod ball joint fastener was not tightened properly. This could cause the fastener to detach and result in loss of steering control.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V134000·2021-03-04

    Ferrara Recalls 2019-2020 Inferno Vehicles for Steering Gear Bolt Issue

    Ferrara Fire Apparatus is recalling 2019-2020 Inferno vehicles because steering gear mounting bolts may loosen, causing steering difficulties and increased crash risk.

    Product
    FERRARA — FERRARA INFERNO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V137000·2021-03-04

    KIA Sportage and Cadenza electrical short circuit poses engine fire risk

    Certain 2017-2021 Sportage and 2017-2019 Cadenza vehicles have a defective hydraulic control unit that may short-circuit and ignite an engine compartment fire. Owners should park outside until repairs are completed.

    Product
    KIA — KIA SPORTAGE, CADENZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21724·2021-03-04

    Polaris Recalls Ranger and ProXD Vehicles Due to Throttle Crash Hazard

    Polaris is recalling approximately 15,800 Ranger and ProXD off-road vehicles because the throttle pedal may stick or return slowly, creating a crash risk.

    Product
    Model Year 2020-2021 RANGER 1000, RANGER CREW 1000, RANGER XP 1000, and RANGER CREW XP 1000 and Model Year 2020 ProXD 2000G, ProXD 2000G H, ProXD 4000G, and ProXD 4000G H
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V139000·2021-03-04

    Nissan Recalls Infiniti FX35 and FX45 Vehicles for Air Bag Defect

    Nissan is recalling specific Infiniti FX35 and FX45 vehicles because a previously replaced front passenger air bag cushion was folded incorrectly, which could tear during deployment.

    Product
    INFINITI — INFINITI FX35, FX45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21725·2021-03-04

    Casa Kids Recalls Cabina Bunk Beds for Fall Hazard

    Casa Kids is recalling Cabina Bunk Beds because loose screws can cause the mattress foundation to fall, posing a risk to children.

    Product
    Cabina Bunk Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0286-2021·2021-03-03

    Cisatracurium Besylate Injection Recalled Due to Labeling Error

    Meitheal Pharmaceuticals is recalling 34,860 vials of Cisatracurium Besylate Injection because cartons were mislabeled as Phenylephrine Hydrochloride.

    Product
    CISATRACURIUM BESYLATE — CISATRACURIUM BESYLATE (CISATRACURIUM BESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0269-2021·2021-03-03

    NDAL Recalls ManukaGuard Nasal Spray Due to Yeast Contamination

    NDAL Mfg Inc. is recalling ManukaGuard Medical Grade Manuka Honey Allercleanse Nasal Spray because the product was confirmed to contain yeast.

    Product
    ManukaGuard Medical Grade Manuka Honey Allercleanse Nasal Spray, 1.3 FL OZ (40mL) bottle, 270 measured sprays, Distributed by Ndal Laboratories, 449 Alvarado St., Monterey, CA 93940 (bottle); NDAL MFG Inc., 80 Garden Court, Suite 100, Monterey, CA 93940 (carton); UPC 8 58631…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0281-2021·2021-03-03

    Teva Recalls MethyIPREDNISolone Acetate Injectable Suspension Due to Sterility Concerns

    Teva Pharmaceuticals is recalling specific lots of MethyIPREDNISolone Acetate Injectable Suspension because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.

    Product
    MethyIPREDNISolone Acetate Injectable Suspension USP, 80 mg/mL, 1 mL Single-Dose Vial (NDC 0703-0051-01), packaged in 25X1ML vials per tray (NDC 0703-0051-04), Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0283-2021·2021-03-03

    Teva Recalls MethyIPREDNISolone Acetate Injectable Suspension Due to Sterility Concerns

    Teva Pharmaceuticals is recalling 6,710 vials of MethyIPREDNISolone Acetate Injectable Suspension because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.

    Product
    MethyIPREDNISolone Acetate Injectable Suspension USP, 200 mg/5 mL (0 mg/mL), 5 mL Multiple-Dose Vial, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-0043-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0277-2021·2021-03-03

    Teva Recalls Metoclopramide Injection Due to Sterility Concerns

    Teva Pharmaceuticals is recalling Metoclopramide Injection because manufacturing areas exceeded microbial acceptance levels, creating a lack of sterility assurance.

    Product
    METOCLOPRAMIDE — METOCLOPRAMIDE (METOCLOPRAMIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0272-2021·2021-03-03

    Teva Recalls Desmopressin Acetate Injection Due to Sterility Concerns

    Teva Pharmaceuticals is recalling Desmopressin Acetate Injection because manufacturing areas exceeded microbial limits, compromising sterility assurance.

    Product
    Desmopressin Acetate Injection USP, 4 mcg/mL, 1 mL Preserved Vial (NDC 0703-5051-01), packaged in 10X1 mL Vials per Tray (NDC 0703-5051-03), Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0276-2021·2021-03-03

    Teva Recalls Leucovorin Calcium Injection Due to Sterility Concerns

    Teva Pharmaceuticals is recalling Leucovorin Calcium for Injection because manufacturing areas exceeded microbial recovery levels, compromising sterility assurance.

    Product
    Leucovorin Calcium for Injection, USP, 100 mg/vial, Single-Dose Vial, Rx only, Teva Parenteral Medicines, Inc., Irvine, CA 92618, NDC 0703-5140-01.
    Category
    Drug
    Distribution
    Distributed nationwide