The Recall Desk

State

American Samoa product recalls

73,598 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 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29851–29875 of 73623

  • LowFDA (Devices)·Z-1244-2020·2020-02-26

    Arrow Epidural Needle Component Recalled for Incorrect Expiration Date

    Arrow International Inc is recalling 1,839 units of Arrow Epidural Needle Component AN-05505 because the product lidstock contains the incorrect expiration date.

    Product
    Arrow EPIDURAL NEEDLE COMPONENT AN-05505
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1241-2020·2020-02-26

    Arrow StimuCath Continuous Nerve Block Kit Recalled for Incorrect Expiration Date

    Arrow International Inc is recalling 155 units of the StimuCath Continuous Nerve Block Kit because the product lidstock contains an incorrect expiration date.

    Product
    Arrow StimuCath(R) Continuous Nerve Block Kit ASK-05060-CHO1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V109000·2020-02-25

    Mercedes-Benz Sprinter Recall for Steering Spindle Bearing Screw Defect

    Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because steering spindle screws may loosen, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 1500, SPRINTER 2500, SPRINTER 4500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V105000·2020-02-25

    Keystone Recalls 2020 Trailers Due to Spare Tire Carrier U-Bolt Failure

    Keystone RV Company is recalling 2020 Crossroads Zinger, Hideout, and Springdale trailers because spare tire carrier U-bolts may fail, allowing the carrier and tire to detach.

    Product
    KEYSTONE — KEYSTONE CROSSROADS ZINGER, HIDEOUT, SPRINGDALE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V110000·2020-02-25

    2019 Mercedes-Benz Sprinter Recall for Missing Steering Column Cover

    Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because the steering column casing cover may be missing, potentially allowing debris to interfere with steering.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 2500, SPRINTER 1500, SPRINTER 3500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V107000·2020-02-24

    Smart Fortwo Electric Drive Recalled for Battery Fire Risk

    Mercedes-Benz is recalling one 2019 Smart Fortwo Electric Drive because a battery weld may detach, causing sudden failure, stalling, or fire.

    Product
    SMART — SMART FORTWO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V104000·2020-02-24

    HME Recalls 2016-2020 Emergency Vehicles Due to Fuse Box Seal Defect

    HME is recalling 2016-2020 AF1, 1871, and SFO emergency vehicles because a missing O-ring seal may allow moisture into the fuse box, potentially causing overheating or malfunction.

    Product
    HME — HME SFO, AF1, 1871
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V099000·2020-02-21

    2021 Ford E-350 Recalled for Rear Axle Differential Fluid Deficiency

    The 2021 Ford E-350 may have inadequate rear axle differential fluid, risking driveshaft separation and loss of drive. Ford will inspect and adjust or replace the rear axle assembly at no cost.

    Product
    FORD — FORD F-550, E-450, E-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V102000·2020-02-21

    CHTC HT-35 and HT-45 Buses Recalled for Non-Compliant Wheelchair Lifts

    CHTC Bus Group is recalling 2016-2018 HT-35 and HT-45 buses because their wheelchair platform lifts failed to complete the required compliance certification process.

    Product
    CHTC BUS — CHTC BUS HT-45, HT-35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E006000·2020-02-20

    Meritor Recall: Insufficient Lubrication in Specific Steer Axles

    Meritor is recalling specific steer axles due to insufficient lubrication that may damage wheel end bearings. This defect could cause the wheel to separate, leading to a loss of vehicle control.

    Product
    POWER TRAIN:AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V096000·2020-02-20

    SMC Laramie Trailers Recalled for Incorrect Tire Pressure Placard

    SMC Trailers is recalling 2019-2020 Laramie trailers because the Federal Placard lists the incorrect tire PSI, which may lead to overinflation and tire failure.

    Product
    SMC — SMC LARAMIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20076·2020-02-20

    Browning Recalls Leather Pistol Holsters Due to Firearm Safety Hazard

    Browning is recalling approximately 1,265 leather pistol holsters because the design can inadvertently change the firearm's safety switch position, posing an injury risk.

    Product
    Browning Leather Pistol Holsters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20075·2020-02-20

    Kolcraft Recalls Inclined Sleeper Accessories for Infant Suffocation Risk

    Kolcraft is recalling inclined sleeper accessories for two bassinet models to prevent infant suffocation. Consumers should stop using the accessory immediately.

    Product
    Inclined sleeper accessory included with Kolcraft Cuddle 'n Care 2-in-1 Bassinet & Incline Sleepers and Preferred Position 2-in-1 Bassinet & Incline Sleepers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1114-2020·2020-02-19

    Teleflex Medical Recalls Hudson RCI Comfort Flo Humidification Systems

    Teleflex Medical is recalling 127,293 Hudson RCI Comfort Flo Humidification Systems nationwide due to a potential risk of water flooding the column and entering the circuit during high-flow oxygen therapy.

    Product
    HUDSON RCI COMFORT FLO Humidification System, REF 2410, humidifier nebulizer kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1115-2020·2020-02-19

    Teleflex Medical Recalls Hudson RCI Comfort Flo Humidification Systems

    Teleflex Medical is recalling 95,696 Hudson RCI Comfort Flo Humidification Systems due to a potential risk of water flooding the column and entering the patient circuit during high-flow oxygen therapy.

    Product
    HUDSON RCI COMFORT FLO Humidification System With Remote Temperature Port, REF 2414, humidifier nebulizer kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1165-2020·2020-02-19

    Pacific Medical Toco M2734A Fetal Monitors Recalled for Unverified Components

    Pacific Medical Group is recalling 466 Toco M2734A fetal monitors serviced with unverified non-OEM components that may fail to detect fetal distress or cause burns.

    Product
    Toco M2734A, that may have been serviced with the following: Pacific Medical Philips Avalon Smart US/TOCO Cable Assembly, NFPHA9020; Pacific Medical Philips Avalon Smart M2734A/2735A Toco Gauge Flex, NFPHA9341
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1108-2020·2020-02-19

    Terumo Advanced Perfusion System 1 Roller Pump Recall for Shaft Failure

    Terumo is recalling 33 Advanced Perfusion System 1 Roller Pumps because the pump shafts may fail, potentially causing the pump to stop during surgery.

    Product
    Terumo Advanced Perfusion System 1 Roller Pump, 4 Inch, Catalog Number 816570 - Product Usage: is indicated for use for up to 6 hours in the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a…
    Category
    Medical Device
    Distribution
    Distributed nationwide