The Recall Desk

State

American Samoa product recalls

73,584 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 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27876–27900 of 73609

  • ModerateFDA (Devices)·Z-2819-2020·2020-08-26

    United Imaging uMI 550 PET/CT Systems Recalled for Software Display Issue

    Shanghai United Imaging Healthcare Co., Ltd. is recalling three uMI 550 PET/CT systems because a software defect may prevent the CT Hounsfield unit curve from displaying in real time during specific scans.

    Product
    Positron Emission Tomography and Computed Tomography System, Model: uMI 550, Material Number: 88000057 - Product Usage: This system is intended to be operated by qualified healthcare professionals to assist in the detection, localization, diagnosis, staging, restaging, treatment…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1516-2020·2020-08-26

    Calvin Scott Recalls Hydrochlorothiazide Tablets Due to Packaging Defect

    Calvin Scott & Company is recalling Hydrochlorothiazide 50mg tablets because light-sensitive products were repackaged in transparent pouches, violating CGMP standards.

    Product
    Hydrochlorothiazide 50mg tablets, 14-count bags, Rx only, Distributed by: Calvin Scott & Co., Inc. Albuquerque, NM 87123, Manufactured by Accord Healthcare, Inc., Durham NC 27703; NDC 16729-0184-17
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2822-2020·2020-08-26

    CareFusion Alaris Pump Module 8100 Recalled for Dim LED Display Segments

    CareFusion 303, Inc. is recalling Alaris Pump Module Model 8100 units because LED display segments may appear dim, potentially affecting the visibility of infusion or patient monitoring values.

    Product
    Alaris Pump Module Model 8100 - Product Usage: is intended to provide trained healthcare caregivers a way to automate the programming of infusion parameters, thereby decreasing the amount of manual steps necessary to enter infusion data.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V500000·2020-08-24

    ETI Recalls 2020 Aerial Lift Trucks Due to Boom Tube Weld Defects

    Equipment Technology is recalling 2020 ETI ETC 37 IH aerial lift trucks because improper welds and steel thickness may cause the platform to fall unexpectedly.

    Product
    ETI — ETI ETC 37 IH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V499000·2020-08-24

    Oshkosh Recalls 2020 S-Series Vehicles for Brake Switch Defect

    Oshkosh is recalling 172 2020 S-Series vehicles because a pressure switch defect may cause air leaks, increased braking distance, or brake light failure.

    Product
    OSHKOSH — OSHKOSH S-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS· 021-2020 ·2020-08-22

    Oberto Recalls Smoked Sausage for Undeclared Soy Allergen

    Oberto Snacks is recalling 309 pounds of smoked sausage due to misbranding and an undeclared soy allergen. No adverse reactions have been reported.

    Product
    Oberto Snacks Inc. — Oberto Snacks, Inc. Recalls Smoked Sausage Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V496000·2020-08-21

    Autocar Recalls 2019 Xpeditor Vehicles for Potential Stalling Hazard

    Autocar is recalling 78 model year 2019 Xpeditor vehicles up-fitted with an aftermarket power take off (PTO) because they may stall or hesitate, increasing the risk of a crash.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E059000·2020-08-21

    Spyder G9 Electronic Control Units Recalled for Fire Risk

    Spyder Controls is recalling G9 electronic control units that can fail under excessive voltage, causing board damage and an increased risk of fire.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E058000·2020-08-21

    Firefly Integrations Recalls Multiplex G9 Units for Fire Risk

    Firefly Integrations is recalling Multiplex G9 units used in motorhomes because excessive voltage can damage the circuit board, increasing the risk of a fire.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V498000·2020-08-21

    Thor Motor Coach motorhomes recalled for potential electrical fire risk

    Thor Motor Coach is recalling 2019-2021 Windsport and Hurricane motorhomes due to a circuit board defect that could cause fire. The electrical control center may be damaged by voltages over 17 volts.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH HURRICANE, WINDSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E057000·2020-08-20

    Motorcar Parts Recalls Duralast Brake Master Cylinders for Volkswagen Models

    Motorcar Parts of America is recalling specific Duralast brake master cylinders for Volkswagen vehicles due to a defect that may cause loss of braking.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:MASTER CYLINDER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V495000·2020-08-20

    2021 BMW Motorcycles Recalled for Detachable Tire Pressure Labels

    BMW is recalling 2021 R 1250 motorcycles (R, RT, RS, GS models) because tire pressure labels may detach from the frame. Without proper tire pressure information readily available, riders risk improper tire inflation, affecting handling and control.

    Product
    BMW — BMW R 1250 RS, R 1250 RT, R 1250 R, R 1250 GS ADVENTURE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1538-2020·2020-08-19

    Itech 361 LLC Recalls All Clean Hand Sanitizer Due to Methanol

    Itech 361 LLC is recalling 18,760 bottles of All Clean Hand Sanitizer because the product contains undeclared methanol.

    Product
    All Clean Hand Sanitizer, Fresh Scent, 1 Liter bottles, Ethyl Alcohol 70.00%, Produced by Eskbiochem SA de CV Ave Mexico Japon 50 Celaya, Gto. Mexico 38010, Distributed by All Clean Natural LTD, UPC Code 6 28055 37013 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1147-2020·2020-08-19

    Wellements Iron Drops Recalled for Undeclared Milk Allergen

    Wellements LLC is recalling Iron Drops liquid dietary supplements because they contain undeclared milk. Consumers with milk allergies should not use the product.

    Product
    Iron Drops (UPC 729609000098) liquid Dietary Supplement, 1 oz/30 mL amber glass bottle packaged in an individual product carton that includes a 1 mL oral syringe dispenser.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1149-2020·2020-08-19

    Upspring Baby Iron Supplement Recalled for Undeclared Milk

    Upspring, Ltd. is recalling 10,328 units of UpSpring Baby Iron + Immunity dietary supplements because they may contain undeclared milk.

    Product
    UpSpring Baby Iron + Immunity MULTI + IRON + ZINC Promotes nutrition For Healthy Growth + Immune System Support For Infants 4 months + Natural Grape Flavor Easy To Use Dropper Dietary Supplement NET WT 2 FL OZ (60 ML)UPC No: 859188006805 packaged in dark brown glass bottles and…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2795-2020·2020-08-19

    Bioseal Trachea Extenders Recalled for Stress Cracks and Leakage Risk

    Bioseal Corporation is recalling 900 units of Trachea Extenders due to stress cracks that may cause breathing system leakage, potentially preventing prescribed ventilation from reaching patients.

    Product
    Bioseal Trachea Extender 1/pl 50pk/Cs, REF TRAX01/50, LOT XXXX, STERILE EO, Single Use Only, Date of Manufacture XXXX, Expiration Date XXXX, LF, UDI: (01) 00630094916019 - Product Usage: Airway connectors intended to connect a breathing gas source to a tracheal tube…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1148-2020·2020-08-19

    Wellements Iron Drops Sampler Recalled for Undeclared Milk

    Wellements LLC is recalling Iron Drops Sampler liquid dietary supplements because the product contains undeclared milk.

    Product
    Iron Drops Sampler (UPC 729609000098) liquid Dietary Supplement, 1 oz/30 mL, (2 mL fill) amber glass bottle packaged in an individual product carton that includes a 1 mL oral syringe dispenser.
    Category
    Food
    Distribution
    Distributed nationwide