The Recall Desk

State

American Samoa product recalls

73,718 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 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30301–30325 of 73743

  • ModerateFDA (Devices)·Z-0874-2020·2020-02-05

    GE Healthcare Recalls SIGNA Premier MRI Systems Due to Date Errors

    GE Healthcare is recalling 62 SIGNA Premier MRI systems because a potential installation issue could cause incorrect dates to be recorded on medical images.

    Product
    SIGNA Premier Nuclear Magnetic Resonance Imaging System - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0912-2020·2020-02-05

    GIBSON Healthcare Membrane Extended Recalled for Incorrect Instructions for Use

    Collagen Matrix Inc is recalling 192 units of GIBSON Healthcare Membrane Extended because they may have been packaged with incorrect Instructions for Use.

    Product
    GIBSON Healthcare Membrane Extended, 30mm x 40mm, Reference Number 5303-342 - Product Usage: Indicated for use in oral surgical procedures as a resorbable material for use in augmentation around implants placed in immediate extraction sockets, delayed extraction sockets…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0823-2020·2020-02-05

    Macleods Pharma Recalls Montelukast Sodium Chewable Tablets for Dissolution Failure

    Macleods Pharma USA is recalling 10,680 bottles of Montelukast Sodium Chewable Tablets, 5 mg, because testing revealed low out-of-specification dissolution results in one lot.

    Product
    MONTELUKAST SODIUM — MONTELUKAST SODIUM (MONTELUKAST SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0911-2020·2020-02-05

    Collagen Matrix Recalls GIBSON Membrane Due to Incorrect Instructions

    Collagen Matrix Inc is recalling 192 units of GIBSON Healthcare Membrane Extended because they may have been packaged with incorrect Instructions for Use.

    Product
    GIBSON Healthcare Membrane Extended, 20mm x 30mm, Reference Number 5303-324 - Product Usage: Indicated for use in oral surgical procedures as a resorbable material for use in augmentation around implants placed in immediate extraction sockets, delayed extraction sockets…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0879-2020·2020-02-05

    Synthes Recalls 2.4mm Sterile Locking Screws Due to Packaging Defect

    Synthes, Inc. is recalling 25 units of 2.4mm sterile locking screws because the packaging may fail to keep the screw accessible, potentially delaying surgery.

    Product
    2.4MM TI VA LOCKING SCREW STARDRIVE 10MM STERILE, Part Number 04.210.110TS - Product Usage:Sterile Tube Packaging is a packaging system to deliver single, sterile screws to the sterile field.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0880-2020·2020-02-05

    Synthes Recalls 2.4mm Sterile Locking Screws Due to Packaging Defect

    Synthes, Inc. is recalling 25 units of 2.4mm sterile locking screws because the packaging may fail to keep the screw sealed, potentially causing surgical delays.

    Product
    2.4MM TI VA LOCKING SCREW STARDRIVE 12MM STERILE, Part Number 04.210.112TS - Product Usage:Sterile Tube Packaging is a packaging system to deliver single, sterile screws to the sterile field.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0859-2020·2020-02-05

    Vitreq Bv Recalls VitreQ 23G Blunt Needles Due to Sterility Risk

    Vitreq Bv is recalling VitreQ 23G Blunt Needles because microscopic tears in the sterile pouch may compromise sterility.

    Product
    VitreQ 23G Blunt Needles with luer-lock connector-REF: CN23.D05 GTIN: 8719214221621
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0875-2020·2020-02-05

    GE Healthcare Recalls SIGNA Architect MRI Systems Due to Date Errors

    GE Healthcare is recalling SIGNA Architect MRI systems because a potential installation issue may cause incorrect dates to be recorded on medical images.

    Product
    SIGNA Architect Nuclear Magnetic Resonance Imaging System - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0877-2020·2020-02-05

    GE Healthcare Recalls MRI Systems Due to Potential Date Setting Error

    GE Healthcare is recalling 62 MRI systems because a potential installation issue may cause incorrect dates to be recorded on medical images.

    Product
    SIGNA Vibrant Nuclear Magnetic Resonance Imaging System, 1.5T Signa HDx, 1.5T Signa HDxt, Signa HDi - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0919-2020·2020-02-05

    Arthrex Fibulock Fibular Nail Instrument Set Recalled for Potential Blockage

    Arthrex, Inc. is recalling 47 units of the Fibulock Fibular Nail Instrument Set due to a potential for blockage of the Hub Attachment Tube.

    Product
    Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0824-2020·2020-02-05

    FDA Recalls Nystatin Oral Suspension for Subpotent Assay Levels

    Pharmaceutical Associates Inc. is recalling Nystatin Oral Suspension because it failed potency testing at 12 months. Patients should stop using the product and consult their healthcare provider.

    Product
    NYSTATIN — NYSTATIN (NYSTATIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0876-2020·2020-02-05

    GE Healthcare Recalls SIGNA Pioneer MRI Systems Due to Date Errors

    GE Healthcare is recalling 62 SIGNA Pioneer MRI systems because an installation issue may cause incorrect dates on medical images.

    Product
    SIGNA Pioneer Nuclear Magnetic Resonance Imaging System - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E003000·2020-02-04

    Cummins Recalls PowerDrive EV Drivetrains for Loss of Drive Power

    Cummins is recalling PowerDrive EV drivetrains for school buses, step vans, and medium-duty trucks because a connector may unplug, causing sudden loss of drive power and power steering.

    Product
    POWER TRAIN recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V061000·2020-02-04

    Hyundai Recalls Vehicles Due to ABS Module Fire Risk

    Hyundai is recalling specific Elantra, Elantra Touring, Santa Fe, and Entourage models because moisture in the ABS module can cause an electrical short and engine compartment fire.

    Product
    HYUNDAI — HYUNDAI SANTA FE, ENTOURAGE, ELANTRA, ELANTRA TOURING
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20T002000·2020-02-04

    Goodyear Recalls Fortera HL Tires Due to Belt Separation Risk

    Goodyear is recalling specific Fortera HL tires because a manufacturing issue may cause belt separation, increasing the risk of a crash.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V060000·2020-01-31

    McElrath Trailers Recalls 2016-2020 Models Due to Frame Weld Cracks

    McElrath Trailers is recalling 2016-2020 VX30-800 and VX50-800 trailers because structural frame welds may crack, increasing crash risk.

    Product
    MCELRATH TRAILERS — MCELRATH TRAILERS VX50-800, VX30-800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V056000·2020-01-31

    Volkswagen Recalls Audi Vehicles for Driver Air Bag Inflator Defect

    Volkswagen Group of America is recalling specific Audi A8, A4, TT, and A6 models because driver air bag inflators may absorb moisture, potentially causing improper deployment in a crash.

    Product
    AUDI — AUDI A8, A4, TT, A6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V054000·2020-01-31

    Triple E Recalls 2020 Motorhomes Due to Propane Line Defects

    Triple E is recalling 237 2020 Unity, Wonder, and Serenity motorhomes because twisted or kinked propane lines may leak and cause a fire.

    Product
    WONDER — WONDER, UNITY, SERENITY W24RTB, W24MB, W24FTB, U24MB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V057000·2020-01-31

    Volkswagen Recalls 2018 Atlas Vehicles Due to Air Bag Sensor Defect

    Volkswagen is recalling 2018 Atlas vehicles because an incorrectly manufactured air bag sensor may delay or disable deployment, increasing injury risk in crashes.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V053000·2020-01-30

    Land Rover Recalls 2020 Discovery Models for Seat Frame Defect

    Jaguar Land Rover is recalling 2020 Discovery vehicles because second-row seat frames may lack fasteners, potentially failing to secure occupants in a crash.

    Product
    LAND ROVER — LAND ROVER DISCOVERY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V055000·2020-01-30

    GM Recalls 2019 Silverado and Sierra Trucks for Brake Software Error

    General Motors is recalling 2019 Chevrolet Silverado 1500 and GMC Sierra 1500 trucks because a software error may disable electronic brake assist, increasing crash risk.

    Product
    GMC — GMC, CHEVROLET SIERRA 1500, SILVERADO 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20716·2020-01-30

    K-Apparel Recalls Children's Lounge Pants Due to Burn Hazard

    K-Apparel is recalling about 2,200 TINFL children's lounge pants because they fail federal flammability standards, posing a burn risk to children.

    Product
    Children's Lounge Pants
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20714·2020-01-30

    Polaris Recalls 2019 Pro XD Utility Vehicles Due to Rear Brake Failure Risk

    Polaris is recalling about 760 Model Year 2019 Pro XD utility vehicles because the rear brake line can puncture, causing rear brake failure and posing a crash hazard.

    Product
    Model Year 2019 Polaris PRO XD Utility Vehicles (UTVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide