The Recall Desk

State

American Samoa product recalls

73,388 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 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22076–22100 of 73413

  • ModerateFDA (Devices)·Z-0509-2022·2022-01-26

    Medichoice Infant Heel Warmer recalled due to unapproved labeling changes

    Philips is recalling 2,925,800 Medichoice Infant Heel Warmer units because labeling was modified beyond the scope of FDA clearance. The devices cannot be sold without new 510(k) approval.

    Product
    Medichoice Infant Heel Warmer, Reference # 989805643721 1079906
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0378-2022·2022-01-26

    Wal-Fex D Allergy and Decongestant Tablets Recalled for Failed Dissolution

    Dr. Reddy's Laboratories is recalling Wal-Fex D Extended Release Tablets nationwide due to failed dissolution specifications. The affected product combines fexofenadine (antihistamine) and pseudoephedrine (decongestant).

    Product
    FEXOFENADINE HCL AND PSEUDOEPHEDRINE HCI — FEXOFENADINE HCL AND PSEUDOEPHEDRINE HCI (FEXOFENADINE HCL AND PSEUDOEPHEDRINE HCI)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0388-2022·2022-01-26

    Drug Recall: Mucus Relief D Subpotent Tablets

    Dr. Reddy's Laboratories is recalling Mucus Relief D (Guaifenesin Pseudoephedrine HCl ER Tablets) nationwide due to subpotency. The affected product was distributed to Walgreen Co. stores across the USA.

    Product
    Mucus Relief D, Guaifenesin Pseudoephedrine HCl ER Tablets, 600 mg/60mg, packaged in 36-count blister pack packed into cartons, Distributed by: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, Made in India, NDC 0363-164-3
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0379-2022·2022-01-26

    Rugby Antihistamine and Decongestant Tablets Recalled for Failed Dissolution

    Dr. Reddy's Laboratories is recalling Rugby brand antihistamine and nasal decongestant tablets nationwide due to failed dissolution specifications. The affected product is NDC 0536-1242-07, Lot #AC2106452F with expiration date 3/31/2023.

    Product
    Rugby, Antihistamine and Nasal Decongestant, Fexofenadine HCl 60mg and Pseudoephedrine HCl 120mg, Extended-Release Tablets USP, 30 Tablets per box, NDC 0536-1242-07, Distributed by: Rugby Laboratories, 17177 N Laurel Park Drive, Suite 233, Livonia, MI, 49152, Made in India.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0380-2022·2022-01-26

    Rite Aid Allergy & Congestion Tablets Fail Dissolution Specifications

    Rite Aid Pharmacy is recalling Allergy & Congestion extended-release tablets because two lots failed to meet dissolution specifications. The affected product was distributed nationwide.

    Product
    Rite Aid Pharmacy, Allergy & Congestion, Fexofenadine HCl 60mg & Pseudoephedrine HCl 120mg, Extended Release Tablets USP, 20 Extended-Release Tablets per box, UPC 011822738873, Distributed by Rite Aid, 30 United Lane, Camp Hill, PA 17011, Made in India.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V029000·2022-01-25

    Forest River Recalls Transit Buses Due to Fire Risk from Relay Module

    Forest River is recalling specific 2021-2023 transit buses because a failed relay module can increase the risk of a fire. Dealers will install a wire jumper harness free of charge.

    Product
    GLAVAL BUS — GLAVAL BUS, STARTRANS, STARCRAFT BUS COMMUTE, SENATOR II HD, ALLSTAR XLT, ALLSTAR XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V030000·2022-01-25

    2021 Harley-Davidson Motorcycles Instrument Cluster May Fail in Cold Weather

    Certain 2021 Harley-Davidson motorcycles may not display the speedometer or neutral indicator at startup in freezing temperatures, creating a crash risk. Owners should contact Harley-Davidson for a free software update.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON RH1250S, RA1250S, RA1250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V031000·2022-01-25

    Kia Recalls Vehicles Due to Potential Air Bag Deactivation

    Kia is recalling specific 2017-2019 models because a defect may prevent air bags from deploying in a crash.

    Product
    KIA — KIA FORTE KOUP, SOUL EV, SEDONA, SOUL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V028000·2022-01-24

    Inland Empire Trailers Recalls 2021 Models Due to Axle Spindle Nut Issues

    Inland Empire Trailers is recalling 50 units of 2021 trailers because improperly tightened axle spindle nuts may cause overheating and loss of control.

    Product
    INLAND EMPIRE TRAILERS — INLAND EMPIRE TRAILERS CUSTOM TRAILER, UTILITY/ DUMP TRAILER, FLAT DECK TRAILER, ENCLOSED TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V027000·2022-01-24

    2022 Mitsubishi Outlander Recalled for Defective Fuel Pump

    Mitsubishi is recalling certain 2022 Outlander vehicles because the fuel pump may fail due to incorrectly fused internal components. Fuel pump failure can cause engine stall, increasing the risk of a crash.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V023000·2022-01-21

    BMW Recalls 2019-2020 K 1600 Motorcycles for Rear Suspension Defect

    BMW is recalling 2019-2020 K 1600 GT, GTL, and B motorcycles because a rear suspension link strut may be insufficiently strong, potentially affecting stability and increasing crash risk.

    Product
    BMW — BMW K 1600 GTL, K 1600 GT, K 1600 B
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V025000·2022-01-21

    Rosenbauer Fire Trucks Recalled for Rear Axle Drive Pinion Fracture Risk

    Rosenbauer America is recalling 127 Commander, Warrior, and Avenger vehicles because a rear axle drive pinion may fracture, potentially engaging the parking brake without warning.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER, WARRIOR, AVENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V022000·2022-01-21

    Kia Recalls 2020 Cadenza for Rear Power Window Safety Issue

    Kia is recalling 2020 Cadenza vehicles because rear power windows can operate after the ignition is off, increasing injury risk.

    Product
    KIA — KIA CADENZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V026000·2022-01-21

    Trails West Recalls 2017-2021 Trailers Due to Propane Regulator Fire Risk

    Trails West is recalling 2017-2021 Sierra, Classic, Santa Fe, and Freeride trailers because a propane regulator may fail, increasing fire risk.

    Product
    TRAILS WEST — TRAILS WEST SIERRA, FREERIDE, CLASSIC, SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E003000·2022-01-20

    Pacific Trailer Recalls RAM A Frame Couplers Due to Welding Defect

    Pacific Trailer is recalling RAM A Frame 2 5/16" couplers because improper welding may cause the trailer to separate from the tow vehicle.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V019000·2022-01-20

    Spartan Fire Vehicles Recalled for Rear Axle Drive Pinion Fracture Risk

    Marion Body Works is recalling 2021-2022 Spartan Fire vehicles because a rear axle drive pinion may fracture, potentially engaging the parking brake without warning and increasing crash risk.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V018000·2022-01-20

    2021-2022 Heartland RVs Recalled for Tire Belt Separation Risk

    Certain 2021-2022 Heartland Cyclone, Fuel, Gravity, and Road Warrior vehicles with Sailun tires may experience belt separation, risking loss of vehicle control. Dealers will replace affected tires at no cost.

    Product
    HEARTLAND — HEARTLAND CYCLONE, GRAVITY, FUEL, ROAD WARRIOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0386-2022·2022-01-19

    Dream Pops Birthday Cake Bites Recalled for Undeclared Milk Allergen

    Dream Pops 100% Plant-Based Birthday Cake Bites are being recalled because they contain undeclared milk, a known allergen that poses a risk to people with milk allergies.

    Product
    100% Plant-Based Dream Pops Birthday Cake Bites UPC 854097008339
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0387-2022·2022-01-19

    Dream Pops Cookie Dough Bites Recalled for Undeclared Milk Allergen

    Dream Pops 100% Plant-Based Cookie Dough Bites are being recalled because they contain undeclared milk allergen. The product was distributed nationwide in the US and Canada.

    Product
    100% Plant-Based Dream Pops Cookie Dough Bites UPC 854097008322
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0369-2022·2022-01-19

    Exela Sodium Bicarbonate Injection Recalled for Sterility Assurance Failure

    Exela Pharma Sciences is recalling 8.4% Sodium Bicarbonate Injection due to lack of assurance of sterility. The affected lot (C0001088/P0001317, expiring 08/2023) was distributed nationwide.

    Product
    8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL), 50 mL vials, Rx Only, Manufactured and Distributed by: Exela Pharma Sciences, LLC., Lenoir, NC 28645, NDC 51754-5001-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0375-2022·2022-01-19

    Clobetasol Propionate Ointment Recalled for Microbial Contamination

    Taro Pharmaceuticals is recalling Clobetasol Propionate Ointment USP 0.05% due to the presence of R. Pickettii bacteria in a non-sterile product. The affected lot may have been distributed nationwide through retailers.

    Product
    CLOBETASOL PROPIONATE — CLOBETASOL PROPIONATE (CLOBETASOL PROPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide