The Recall Desk

State

American Samoa product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43526–43550 of 73834

  • LowFDA (Drugs)·D-0692-2017·2017-05-10

    Aripiprazole Tablets Recalled for Out-of-Specification Assay Results

    The Harvard Drug Group is recalling Aripiprazole Tablets, 2 mg, due to out-of-specification assay results. The recall covers 36,990 tablets distributed nationwide and in Puerto Rico.

    Product
    Aripiprazole Tablets, 2 mg, 30 count unit dose box, Rx only, Manufactured by Apotex Inc., Toronto, Ontario, Canada, Distributed by Major Pharmaceuticals, Livonia, MI NDC 0904-6509-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1949-2017·2017-05-10

    Anspach Effort Recalls Electronic Foot Controls Due to Missing Service Interval

    The Anspach Effort, Inc. is recalling 821 Electronic Foot Controls because the supplied directions for use did not contain a recommended service interval.

    Product
    Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1936-2017·2017-05-10

    Anspach Effort AL-III-DISS Adapter Recall for Missing Service Interval

    The Anspach Effort, Inc. is recalling five AL-III-DISS Adapters because the supplied directions for use did not contain a recommended service interval.

    Product
    AL-III-DISS Adapter Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1956-2017·2017-05-10

    Anspach Effort Recalls System Consoles for Missing Service Interval Instructions

    The Anspach Effort, Inc. is recalling 462 System Console units because the supplied directions for use did not contain a recommended service interval.

    Product
    System Console, Single Port, with irrigation Product Usage: Electric system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V302000·2017-05-09

    FCA Recalls Ram Trucks Due to Disabled Side Curtain Air Bags

    FCA US LLC is recalling 2013-2016 Ram 1500, 2500, and 3500 trucks because a sensor fault may disable side curtain air bags and seat belt pretensioners, increasing injury risk in crashes.

    Product
    RAM — RAM 1500, 3500, 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-050917·2017-05-09

    FSIS Public Health Alert for Frozen Pork and Chicken Due to Listeria

    The USDA FSIS issued a public health alert for frozen ready-to-eat fried chicken and pork sausage products due to possible Listeria monocytogenes contamination. No illnesses have been reported.

    Product
    FSIS Issues Public Health Alert for Pork and Poultry Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·17744·2017-05-09

    Honda Recalls 2017 Pioneer 700 Vehicles Due to Seat Belt Defect

    American Honda is recalling about 2,200 2017 Pioneer 700 recreational off-highway vehicles because a manufacturing defect may cause the front passenger seat belt buckle to fail.

    Product
    Recreational off-highway vehicles (ROVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V306000·2017-05-08

    Forest River Recalls 2017 XLR ToyHaulers for Incorrect Tire Pressure Label

    Forest River is recalling 2017 XLR ToyHauler trailers because the Federal Placard incorrectly lists rear tire pressure as 50psi instead of 80psi, which could lead to tire failure.

    Product
    FOREST RIVER — FOREST RIVER XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E023000·2017-05-05

    TRW Recalls Aftermarket Lower Ball Joints for Toyota Vehicles

    TRW is recalling aftermarket lower ball joints for Toyota 4Runner, Sequoia, and Tundra vehicles because a design defect could cause steering loss and increase crash risk.

    Product
    SUSPENSION:FRONT:CONTROL ARM:LOWER BALL JOINT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide