The Recall Desk

State

American Samoa product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30526–30550 of 73747

  • HighNHTSA·20V022000·2020-01-17

    Hyundai Recalls 2020 Kona Vehicles for Incorrect Weight Rating Label

    Hyundai is recalling 2020 Kona vehicles because the certification label may display an incorrect Gross Axle Weight Rating. Dealers will replace the label to ensure compliance with federal safety standards.

    Product
    HYUNDAI — HYUNDAI KONA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V025000·2020-01-17

    Isuzu and Chevrolet Trucks Recalled for Seat Belt Webbing Defect

    Isuzu and Chevrolet trucks are being recalled because a manufacturing issue may prevent the seat belt webbing locking mechanism from properly restraining occupants.

    Product
    ISUZU — ISUZU, CHEVROLET NPR HD, NRR, NPR XD, 4500HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V021000·2020-01-16

    Multiquip Recalls 2019 WT5C Trailers Due to Safety Chain Defect

    Multiquip is recalling 119 2019 WT5C trailers because incorrect safety chain attachment points may interfere with steering and increase crash risk.

    Product
    MULTIQUIP — MULTIQUIP WT5C
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20052·2020-01-16

    Baby Trend Recalls Tango Mini Strollers Due to Fall Hazard

    Baby Trend is recalling about 2,000 Tango Mini Strollers because hinge joints can release and collapse, posing a fall hazard to children.

    Product
    Tango Mini Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalNHTSA·20V018000·2020-01-15

    BMW Recalls 2000-2006 Models for Airbag Inflator Explosion Risk

    BMW is recalling 2000-2006 3-Series and M3 vehicles because front passenger airbag inflators may explode, sending metal fragments into the cabin.

    Product
    BMW — BMW 323IT, M3, 323I, 330CI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0496-2020·2020-01-15

    Reichel Foods Recalls Pro2Snax Snack Trays Due to Listeria Contamination

    Reichel Foods Inc. is recalling Pro2Snax To The Max snack trays nationwide due to Listeria monocytogenes contamination.

    Product
    Pro2Snax To The Max snack tray containing Sweet Gala Apples, Hard Boiled Egg, White Cheddar Cheese, and Dried Cranberries & Almonds. Item # 1-4550-6. Net Wt. 7.35 oz (208g) UPC 6 49632-00148 3 Keep Refrigerated.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V016000·2020-01-15

    BMW Recalls X5 and X6 Models Due to Air Bag Inflator Defect

    BMW is recalling specific X5 and X6 models because passenger air bag inflators may explode, posing a risk of serious injury or death.

    Product
    BMW — BMW X5, X6, X6 ACTIVEHYBRID SAC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V014000·2020-01-15

    Triumph Recalls 2019-2020 Speed Twin Motorcycles for Gear Shift Defect

    Triumph is recalling 2019-2020 Speed Twin motorcycles because the gear shift lever linkage may separate, potentially preventing gear changes and increasing crash risk.

    Product
    TRIUMPH — TRIUMPH SPEED TWIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V017000·2020-01-15

    BMW Recalls Vehicles for Driver Air Bag Inflator Explosion Risk

    BMW is recalling specific 2006-2015 models because driver air bag inflators may explode due to propellant degradation, posing a risk of serious injury or death.

    Product
    BMW — BMW 330I, 330XI, 128I, 1 SERIES M
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V019000·2020-01-15

    Winnebago Recalls 2020 Adventurer Motorhomes Due to Fire Risk

    Winnebago is recalling 2020 Adventurer motorhomes because a heat coil may fail to disengage, increasing the risk of a fire.

    Product
    WINNEBAGO — WINNEBAGO ADVENTURER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0780-2020·2020-01-15

    Stryker T2 Alpha Delta Strike Plate Recalled for Breakage Risk

    Stryker GmbH is recalling T2 Alpha Delta Strike Plate instruments because they can break during nail implantation or removal, potentially causing complications.

    Product
    Stryker T2 Alpha Delta Strike Plate IMN Instruments - part of the IMN Instruments System and is used to support insertion and withdrawal of nails through the Targeting Device Catalog Number: 2351-0050
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0495-2020·2020-01-15

    Reichel Foods Recalls Pro2Snax Snack Trays Due to Listeria Contamination

    Reichel Foods Inc. is recalling Pro2Snax To The Max snack trays due to Listeria monocytogenes contamination. The affected products were distributed nationwide.

    Product
    Pro2Snax To The Max snack tray containing Sliced Apples, Hard Boiled Egg, Mild Cheddar Cheese, and Dried Cranberries & Cashews. Item # 1-4555-6. Net Wt. 7.35 oz (208g) UPC 6 49632-00149 0 Keep Refrigerated.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0789-2020·2020-01-15

    Abbott Recalls Fast-Cath Hemostasis Introducers Due to Incorrect Size

    Abbott Medical is recalling 380 Fast-Cath Hemostasis Introducers because three lots contained 8F components instead of the labeled 8.5F size.

    Product
    Fast-Cath Hemostasis Introducer, HEMOSTASIS INTRODUCER, 8.5F, 2.83 mm, REF 406143 - Product Usage: The Fast-Cath Hemostasis Introducers are indicated for the introduction of angiographic catheters, closed-end catheters, balloon catheters, and electrodes into a vessel where…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0793-2020·2020-01-15

    Baxter Recalls Clearlink Continu-Flo Administration Sets Due to Connection Force Issue

    Baxter Healthcare is recalling Clearlink System Continu-Flo Administration Sets because some units require higher-than-expected force to connect securely.

    Product
    Clearlink System Continu-Flo Administration Sets, Product Codes: 2C8519, 2C8537, and 2C8541 - Product Usage:For the administration of fluids from a container into the patients vascular system through a vascular access device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0784-2020·2020-01-15

    Intersurgical Double Swivel Elbow Airway Connectors Recalled for Cracking Risk

    Intersurgical Inc is recalling 115,200 Double Swivel Elbow airway connectors because the port may crack and leak.

    Product
    Double Swivel Elbow with Bronchoscopy Port 15MM OD, 22MM OD/15MM ID, REF 1898000. Airway connector.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0775-2020·2020-01-15

    Medacta Shoulder Implant Recall Due to Screw Insertion Limitation

    Medacta USA Inc. is recalling specific lots of Humeral Anatomical Cementless Metaphysis implants because a dimensional condition may limit the insertion of the locking screw.

    Product
    Medacta Shoulder SYSTEM HUMERAL ANATOMICAL METAPHYSIS, REF 04.01.0023 through 04.01.0055, all sizes - Product Usage: The Medacta Anatomic Shoulder Prosthesis is indicated for treatment of humeral fractures and for primary or revision total shoulder replacement in patients with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0788-2020·2020-01-15

    Avanos Recalls Haylard Closed Suction Systems Due to Blocked Lumens

    Avanos Medical is recalling Haylard Closed Suction Systems for neonates and pediatrics because the central lumen may be blocked, potentially preventing adequate suctioning of airway secretions.

    Product
    Haylard Closed Suction System for Neonates/Pediatrics, 5 Fr, 1. REF 195, Y-Adapter, SAP Finished Product Code 109382303; 2. REF 201, with BALLARD Technology, SAP Finished Product Code 109382803; 3. REF 202, Elbow, SAP Finished Product Code 109382903; 4. REF 195-5…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0782-2020·2020-01-15

    Siemens Cios Alpha Mobile X-Ray System Recalled for C-Arm Holder Crack

    Siemens Medical Solutions is recalling Cios Alpha mobile X-ray systems because a crack in the C-arm holder could compromise stability and lead to injury.

    Product
    Cios Alpha, Model Number 10308191; mobile X-Ray system designed to provide X-ray imaging of the anatomical structures of patient during clinical application
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0787-2020·2020-01-15

    Intersurgical Airway Connector Recalled for Potential Swivel Elbow Cracking

    Intersurgical Inc is recalling 50,400 airway connectors because the swivel elbow port may crack and leak. The recall covers products distributed nationwide in the US.

    Product
    Superset with 22MM ID, Double Swivel Elbow 22MM OD/15MM ID and Bronchoscopy Port, REF 3521000. Airway connector.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0781-2020·2020-01-15

    Stryker Pin To Rod Coupling Recalled for Clamping Failure

    Stryker is recalling Pin To Rod Couplings for the Hoffmann II Compact External Fixation System because they may fail to clamp the pin and rod as intended.

    Product
    Stryker Pin To Rod Coupling External Fixation System Hoffmann II Compact - Pin To Rod Coupling 5/3-4mm Catalog #: 4940-1-020 - Product Usage: Indications Distal radius fractures (intra and extra) articular Intercarpal fracture dislocations Unstable forearm fractures…
    Category
    Medical Device
    Distribution
    Distributed nationwide