The Recall Desk

State

American Samoa product recalls

73,576 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 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27701–27725 of 73601

  • ModerateFDA (Devices)·Z-2929-2020·2020-09-09

    Stimwave StimQ Peripheral Nerve Stimulator System Recalled for Non-Functional Component

    Stimwave Technologies is recalling 1,550 StimQ Peripheral Nerve Stimulator Systems because they contain a non-functional component not referenced in product labeling.

    Product
    StimQ Peripheral Nerve Stimulator System (PNS) Model FR4A-TRL-AO US - Product Usage: is used for peripheral neural stimulation to provide therapeutic relief for chronic, intractable pain of peripheral nerve origin. The therapy utilizes pulsed electrical current to create an…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2932-2020·2020-09-09

    Stimwave StimQ Peripheral Nerve Stimulator Recalled for Non-Functional Component

    Stimwave Technologies is recalling 2,197 StimQ Peripheral Nerve Stimulator units because they contain a non-functional component not listed in the product labeling.

    Product
    StimQ Peripheral Nerve Stimulator System (PNS) Model STQ4-SPR-BO US - Product Usage: is used for peripheral neural stimulation to provide therapeutic relief for chronic, intractable pain of peripheral nerve origin. The therapy utilizes pulsed electrical current to create an…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2872-2020·2020-09-09

    GE Healthcare Recalls OEC 9800 and 9900 C-Arms for Dose Display Issues

    GE Healthcare is recalling 221 OEC 9800 and 9900 C-Arms because field service engineers changed the dose display to DAP, violating FDA regulations requiring AKR/CAK.

    Product
    The OEC 9900 C-Arm is designed to provide fluoroscopic and spot-film images of the patient during diagnostic, surgical and interventional procedures. Examples of clinical application may include cholangiography, endoscopy, urologic, orthopedic, neurologic, vascular, cardiac…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2933-2020·2020-09-09

    Stimwave StimQ Peripheral Nerve Stimulator Recalled for Non-Functional Component

    Stimwave Technologies is recalling 13 StimQ Peripheral Nerve Stimulator units because they contain a non-functional component not listed in the product labeling.

    Product
    StimQ Peripheral Nerve Stimulator System (PNS) Models: 1. FR4A-RCV-AO US and 2. FR4A-RCV-A0 EU - Product Usage: is used for peripheral neural stimulation to provide therapeutic relief for chronic, intractable pain of peripheral nerve origin. The therapy utilizes pulsed…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2930-2020·2020-09-09

    Stimwave StimQ Peripheral Nerve Stimulator Recalled for Non-Functional Component

    Stimwave Technologies is recalling 1,424 StimQ Peripheral Nerve Stimulator units because they contain a non-functional component not referenced in product labeling.

    Product
    StimQ Peripheral Nerve Stimulator System (PNS) Models: 1. FR4A-TRL-BO US and 2. FR4A-TR-BO - Product Usage: is used for peripheral neural stimulation to provide therapeutic relief for chronic, intractable pain of peripheral nerve origin. The therapy utilizes pulsed electrical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2931-2020·2020-09-09

    Stimwave StimQ Peripheral Nerve Stimulator System Recalled for Non-Functional Component

    Stimwave Technologies is recalling six StimQ Peripheral Nerve Stimulator Systems because they contain a non-functional component not referenced in product labeling.

    Product
    StimQ Peripheral Nerve Stimulator System (PNS) Models FR4A-SPR-BO US - Product Usage: is used for peripheral neural stimulation to provide therapeutic relief for chronic, intractable pain of peripheral nerve origin. The therapy utilizes pulsed electrical current to create an…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1557-2020·2020-09-09

    Santa Cruz Recalls Subpotent UltraCruz Hand Sanitizing Gel

    Santa Cruz Biotechnology is recalling 14,238 bottles of UltraCruz Hand Sanitizing Gel because the product is subpotent.

    Product
    UltraCruz Hand Sanitizing Gel Antimicrobial (70% Isopropyl Alcohol), packaged in 3 Fluid Oz./89 mL bottes, Manufactured By Santa Cruz Biotechnology, Inc. 10410 Finnell St. Dallas, TX 75220
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2914-2020·2020-09-09

    Cardinal Health Recalls PROTEXIS Latex Micro Surgical Gloves Due to Defects

    Cardinal Health 200, LLC is recalling PROTEXIS Latex Micro Surgical Gloves because a degradation defect could cause holes and tears at the cuffs.

    Product
    PROTEXIS Latex Micro Surgical Gloves Size 6.5 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic rubber intended to be worn by operating room personnel to be a barrier protection from contamination. Various thickness for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V545000·2020-09-08

    Autocar Recalls 2019 Xpeditor Vehicles for Methane Detection Wiring Fire Risk

    Autocar is recalling 170 2019 Xpeditor vehicles equipped with factory-installed methane detection systems because inadequate circuit protection may cause the wiring harness to overheat, increasing the risk of a fire.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V544000·2020-09-08

    2021 Coachmen Catalina Recalled Due to Griddle Fire Risk

    Forest River is recalling 2021 Coachmen Catalina trailers because a long griddle hose allows open flames to be stowed inside, increasing fire risk.

    Product
    COACHMEN — COACHMEN CATALINA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V543000·2020-09-04

    Hyundai Tucson 2016-2021: Engine Compartment Fire from Brake Control Unit

    Hyundai is recalling 2016-2021 Tucson vehicles because the Anti-lock Brake Hydraulic Electronic Control Unit could corrode and cause an electrical short, creating a risk of engine compartment fire.

    Product
    HYUNDAI — HYUNDAI TUCSON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-09042020-01·2020-09-04

    USDA Issues Public Health Alert for Ineligible Imported Cooked Duck Blood Curds

    USDA FSIS issued a public health alert for imported cooked duck blood curds from China that lack required inspection certificates, making them unfit for human consumption.

    Product
    FSIS Issues Public Health Alert for Ineligible Imported Cooked Duck Blood Curds from China
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·20V540000·2020-09-04

    2021 Forest River Berkshire Motorhomes Recalled for Inverter Overload Fire Risk

    Forest River is recalling 2021 Berkshire motorhomes with 3000W inverters that overload electrical wiring and create a fire risk. Owners should contact Forest River at 1-754-533-5934 for a free replacement inverter.

    Product
    FOREST RIVER — FOREST RIVER BERKSHIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20776·2020-09-03

    CFMOTO Recalls 2020 ZFORCE 950 Sport Vehicles Due to Fire Hazard

    CFMOTO is recalling 2020 ZFORCE 950 Sport vehicles because a fuel line fitting may fail to lock, causing fuel leaks and fire.

    Product
    2020 ZFORCE 950 Sport Recreational Off-Highway Vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V538000·2020-09-03

    2021 Keystone Fuzion and Impact Trailers Fuel Tank Mounting Bolts Recall

    Keystone is recalling certain 2021 Fuzion and Impact recreational trailers with improperly secured auxiliary fuel supply tank mounting bolts. The defective grade 2 bolts may break, causing the tank to detach and increasing risk of fire or vehicle crash.

    Product
    KEYSTONE — KEYSTONE FUZION, IMPACT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20774·2020-09-03

    StoreYourBoard Recalls Hi-Lift Storage Hoists Due to Strap Breakage Hazard

    StoreYourBoard.com is recalling Hi-Lift Storage Hoists because green polypropylene straps can break, causing stored items to fall and potentially injure passersby.

    Product
    Hi-Lift Storage Hoist Classic and Pro models sold with green polypropylene straps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20775·2020-09-03

    SODA SENSE Recalls CO2 Canisters Due To Valve Ejection Injury Hazard

    SODA SENSE is recalling about 19,200 CO2 canisters because a valve can break and eject, posing an injury hazard. No injuries have been reported, but minor property damage has occurred.

    Product
    SODA SENSE® CO2 canisters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V539000·2020-09-03

    Western Star and Freightliner trucks recalled for suspension hardware defect

    Daimler Trucks recalls 2020-2021 Western Star 4700 and 4900, and Freightliner 114SD and 122SD trucks due to suspension axle hardware that may be insufficiently long to engage locking nuts, creating road hazards and crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR 122SD, 4900, 114SD, 4700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V537000·2020-09-03

    2021 Chevrolet Trailblazer and 2020 Buick Encore GX Seat Fastener Recall

    General Motors is recalling 2021 Chevrolet Trailblazers and 2020 Buick Encore GX vehicles because front seat rear attachment bolts may not have been installed, potentially allowing seats to move during a crash.

    Product
    BUICK — BUICK, CHEVROLET ENCORE, TRAILBLAZER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1274-2020·2020-09-02

    Thomson International Recalls White Onions Linked to Salmonella Outbreak

    Thomson International is recalling white onions packed under Thomson Premium, Onions 52, and El Competitor brands due to a link to a Salmonella Newport outbreak.

    Product
    White onions; Packed under brand names of Thomson Premium, Onions 52, El competitor. Thomson Premium: 25 lb. mesh sack -No UPC 50 lb. mesh sack -No UPC Onions 52: 8 lb. mesh bag - UPC 8 15222 01019 1 El Competitor 50 lb. mesh sack - No UPC
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1272-2020·2020-09-02

    Red Onions Recalled Due to Salmonella Newport Outbreak Investigation

    Thomson International is recalling red onions nationwide and in Canada because a traceback investigation linked them to a Salmonella Newport outbreak.

    Product
    Red onions; Packed under brand names of Thomson Premium, Onions 52, Utah Onions, Harley's Best, Onions 52, Imperial Fresh, TLC Thomson International, El Competidor Thomson Premium packed in 50 and 25 lb.mesh sack, and 2 lb. mesh sack - UPC 33383 60101 3 lb. mesh sack…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1534-2020·2020-09-02

    Medichem Recalls Chlorhexidine Gluconate Due to Serratia marcescens Contamination

    Medichem S.A. is recalling Chlorhexidine Gluconate 0012 for manufacturing due to microbial contamination with Serratia marcescens.

    Product
    Chlorhexidine Gluconate 0012 For Manufacturing, Processing or Repacking, RX Only, Medichem, S.A. Poligono Industrial Celra, 17460, Celra, Girona (Spain/Espana); Fructuos Gelabert, 6-8, 08970, Sant Joan Despi, Barcelona (Spain/Espana) NDC 53296-0012-0
    Category
    Drug
    Distribution
    Distributed nationwide