The Recall Desk

State

American Samoa product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40801–40825 of 73831

  • HighFDA (Devices)·Z-0026-2018·2017-10-25

    CareFusion Recalls Alaris Pump Modules Due to Flow Rate Variations

    CareFusion 303, Inc. is recalling Alaris Pump Module model 8100 units due to reports of increased or decreased medication flows.

    Product
    Alaris Pump Module model 8100 manufactured between November 2011 and March 2012; Alaris Pump Module serviced with LVP Mechanism Sub Assembly (P/N) 10942012 between November 2011 and March 2012; Alaris Pump module Bezel Kit Assembly (P/N) 10964559) shipped between November…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0029-2018·2017-10-25

    Bel Brands Recalls Merkts Port Wine Cheese Spread Due to Foreign Material

    Bel Brands USA is recalling Merkts Port Wine Cheese Spread after customers reported finding white plastic pieces in the product.

    Product
    Merkts Port Wine Cheese Spread, Net Wt. 14 oz (396g), UPC 76306-60200
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·18016·2017-10-25

    PlanToys Recalls Baby Gyms Due to Strangulation Hazard

    PlanToys is recalling about 500 baby gyms sold in 2016 and 2017 because babies can strangle on the side rope crossbars. No injuries have been reported.

    Product
    Baby Gym
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0025-2018·2017-10-25

    Medtronic Recalls VCLAS Laser Applicators Due to Saline Leakage Testing Defect

    Medtronic is recalling 423 VCLAS laser applicator systems because they were not appropriately tested for saline leakage during manufacturing.

    Product
    VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559 Visualase Cooled Laser Applicator System 3mm Tip; Part Number: 9735560 Visualase Cooled Laser Applicator System 10mm Tip; Part Number: 9735561 Visualase Cooled Laser Applicator System 15mm Tip
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0010-2018·2017-10-25

    Unichem Recalls Bisoprolol Fumarate Tablets Due to Stability Impurity

    Unichem Pharmaceuticals is recalling 96,876 bottles of Bisoprolol Fumarate 5 mg tablets because stability testing revealed an out-of-specification unknown impurity.

    Product
    BISOPROLOL FUMARATE — BISOPROLOL FUMARATE (BISOPROLOL FUMARATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0020-2018·2017-10-25

    Philips Brilliance iCT SP CT Systems Recalled for Image Reconstruction Failure

    Philips is recalling Brilliance iCT SP CT systems because a software defect prevents image reconstruction after bolus tracking scans, potentially requiring patients to be rescanned.

    Product
    Philips Healthcare Brilliance iCT SP X-Ray, Tomography, Computed These computed tomography x-ray systems are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0015-2018·2017-10-25

    Philips Brilliance 64 CT Systems Recalled for Image Reconstruction Failure

    Philips Electronics North America Corporation is recalling 606 Brilliance 64 CT systems in the US because a software defect prevents image reconstruction after certain scans.

    Product
    Philips Healthcare Brilliance 64 System, X-Ray, Tomography, Computed These computed tomography x-ray systems are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0016-2018·2017-10-25

    Philips Ingenuity Core CT Systems Recalled for Image Reconstruction Failure

    Philips is recalling 606 Ingenuity Core CT systems in the US because a software defect prevents image reconstruction after bolus tracking scans.

    Product
    Philips Healthcare Ingenuity Core X-Ray, Tomography, Computed These computed tomography x-ray systems are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0039-2018·2017-10-25

    Teleflex Pilling Knife Handles Recalled for Blade Fit Issues

    Teleflex Medical is recalling Pilling Knife Handles because the slot depth is out of specification, which may prevent blades from fitting properly.

    Product
    Pilling Knife Handles: a) REF 352950 b) REF 352953 c) REF 352951 d) REF 352957 e) REF 352952 : Reusable surgical knife handles, which are intended for use with blades which are inserted into a slot in the handle.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0019-2018·2017-10-25

    Philips Brilliance iCT CT Scanner Recall for Data Reconstruction Failure

    Philips is recalling Brilliance iCT CT scanners because a software defect prevents image reconstruction after bolus tracking scans, potentially requiring patients to be rescanned.

    Product
    Philips Healthcare Brilliance iCT X-Ray, Tomography, Computed These computed tomography x-ray systems are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0012-2018·2017-10-25

    Toshiba Medical Kalare Fluoroscopic X-Ray System Recalled for Image Display Failure

    Toshiba American Medical Systems Inc is recalling 96 Kalare Fluoroscopic X-Ray Systems because images may fail to display on the system monitor or save to the hard disk.

    Product
    Toshiba Medical Kalare Fluoroscopic X-Ray System (DREX-KL80) Kalare is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic examinations, including general R&F and pediatric examinations. It is intended for use by…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0018-2018·2017-10-25

    Philips Ingenuity Core128 CT Systems Recalled for Image Reconstruction Failure

    Philips is recalling Ingenuity Core128 CT systems because a software defect prevents image reconstruction after bolus tracking scans, potentially requiring patient rescans.

    Product
    Philips Healthcare Ingenuity Core128 X-Ray, Tomography, Computed These computed tomography x-ray systems are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0017-2018·2017-10-25

    Philips Ingenuity CT Systems Recalled for Bolus Tracking Image Failure

    Philips is recalling Ingenuity CT systems because a software defect prevents image generation during bolus tracking procedures, potentially requiring patient rescans.

    Product
    Philips Healthcare Ingenuity CT X-Ray, Tomography, Computed These computed tomography x-ray systems are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V670000·2017-10-24

    2018 Jeep Cherokee and Compass Recall for Oil Pump Housing Defect

    Chrysler is recalling 2018 Jeep Cherokee and Compass vehicles with 2.4L engines due to a cracked oil pump housing that can cause engine stalling and increase crash risk.

    Product
    JEEP — JEEP CHEROKEE, COMPASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18015·2017-10-24

    Fisher-Price Recalls Soothing Motions Seats Due to Fire Hazard

    Fisher-Price is recalling Soothing Motions Seats because the motor housing can overheat, posing a fire hazard. No injuries have been reported.

    Product
    Soothing Motions Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V668000·2017-10-23

    Ford Recalls 2015-2017 Transit Vehicles for Electrical Wiring Fire Risk

    Ford is recalling 2015-2017 Transit vehicles with trailer tow modules because water intrusion can corrode wiring, potentially causing electrical shorts, fires, or crashes.

    Product
    FORD — FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V672000·2017-10-23

    Ford Recalls 2018 F-150 Trucks Due to Engine Lubrication Defect

    Ford is recalling 2018 F-150 trucks with 3.5L engines because cylinder heads may lack lubrication holes, risking engine failure and crashes.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V669000·2017-10-23

    Ford Recalls 2018 F-150 Trucks for Transmission Shift Lever Defect

    Ford is recalling 2018 F-150 trucks with 3.3L engines and column shift levers because quickly moving the lever may cause unintended gear selection, increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18013·2017-10-20

    BSH Expands Recall of Bosch, Gaggenau, Jenn-Air, and Thermador Dishwashers

    BSH Home Appliances is expanding a recall of approximately 408,000 dishwashers due to a fire hazard caused by overheating power cords. No injuries have been reported, but five property damage incidents have occurred.

    Product
    Bosch, Gaggenau, Jenn-Air and Thermador brand dishwashers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17E063000·2017-10-20

    Aperia Halo Tire Inflator Recall Due to Bracket Failure Risk

    Aperia Technologies is recalling Halo Tire Inflators because adapter plate brackets may crack, causing rapid tire deflation and increased crash risk.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V667000·2017-10-20

    Keystone Recalls Crossroads RVs Due to Outdoor Cook Top Fire Risk

    Keystone is recalling specific 2017-2018 Crossroads recreational vehicles because the outdoor cook top's fiber board can burn if flames invert, creating a fire hazard.

    Product
    CROSSROADS — CROSSROADS SUNSET, ZINGER, VOLANTE, CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V664000·2017-10-19

    GM Recalls 2011-2015 Silverado and Sierra 3500 Trucks for Fuel Leak Risk

    General Motors is recalling 2011-2015 Chevrolet Silverado 3500 and GMC Sierra 3500 trucks because a stuck fuel sensor may cause the front tank to overfill, potentially leading to a fuel leak and fire.

    Product
    GMC — GMC, CHEVROLET SIERRA 3500, SILVERADO 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide