The Recall Desk

State

American Samoa product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35101–35125 of 73766

  • HighFDA (Devices)·Z-0939-2019·2019-03-06

    Merge Eye Station Retinal Imager Recalled for Electrical Safety Defects

    Merge Healthcare is recalling 1,252 WinStation Retinal Imagers because certain configurations may produce electrical output exceeding allowable medical device limits.

    Product
    The WinStation Retinal Imager, also known as Merge Eye Station. DCF-1024 & DCF-512 Digital Imaging System Product Usage: The WinStation Retinal Imager has the same intended use as other fundus cameras. It is specifically used to produce color or black and white images of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0949-2019·2019-03-06

    Arrow AutoFuser Disposable Pain Control Pump Recalled for Potential Cracks

    Arrow International Inc. is recalling 9 units of the Arrow AutoFuser Disposable Pain Control Pump due to possible cracks on the fill port connector that may cause leaks.

    Product
    AF 550 x 5ML/HR CPNB, Product code MC0050XL CPNB, Arrow AutoFuser Disposable Pain Control Pump
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0872-2019·2019-03-06

    Philips Multiva MRI System Recalled for Ceiling Speaker Hazard

    Philips is recalling Multiva 1.5T MRI systems because ceiling speakers may fall due to magnetic attraction.

    Product
    Multiva 1.5T 16 R5 (ZBO), Model Number 781073. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0887-2019·2019-03-06

    Philips MRI System Recall for Falling Ceiling Speaker Hazard

    Philips is recalling Intera Achieva 1.5T Pulsar MRI systems because ceiling speakers may fall due to magnetic attraction.

    Product
    Intera Achieva 1.5T Pulsar, Model Number 781171. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0961-2019·2019-03-06

    Alcon Ophthalmic Microscope Recalled for Potential Optical Head Detachment

    Alcon is recalling LuxOr E71 and E71 Q-Vue ophthalmic microscopes because the optical head may detach from the stand due to missing thread adhesive.

    Product
    Alcon or Endure Ophthalmic Microscope Product Usage: Used for low magnification visualization during ophthalmic surgical procedures for cataract, retina and cornea.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0925-2019·2019-03-06

    Philips MR-OR 3.0T MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling 11,226 MR-OR 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    MR-OR 3.0T, Model Number 781438. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0899-2019·2019-03-06

    Philips Achieva XR MRI Systems Recalled for Falling Speaker Hazard

    Philips is recalling Achieva XR MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva XR 1.5T/3.0T , Model Number 781253. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0909-2019·2019-03-06

    Philips Achieva MRI Systems Recalled Due to Ceiling Speaker Hazard

    Philips is recalling 11,226 Achieva 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva 1.5T, Model Number 781296. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1097-2019·2019-03-06

    Planetary Herbals Mullein Lung Complex Recalled for Labeling Error

    Planetary Herbals is recalling Mullein Lung Complex capsules due to a labeling error regarding inactive ingredients.

    Product
    Planetary Herbals Mullein Lung Complex; 1000 mg; 15 count, item number PF0003; 90 count - Item number PF0002; 180 count, Item number PF0106 and 90 + 90 count, PF 7013 white plastic bottles. Proprietary Blend: Platycodon root, Ophiopagon Rhizome, Long Pepper Fruit, Black…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0967-2019·2019-03-06

    Cook Inc. Recalls Gastrointestinal Suture Anchor Sets Due to Retention Mechanism Issue

    Cook Inc. is recalling 797 Entuit Secure Gastrointestinal Suture Anchor Sets because a specific extension spring lot may cause difficulty sliding the retention mechanism.

    Product
    Entuit Secure Gastrointestinal Suture Anchor Set, Catalog Number GIAS-SRM-2, Order Number G35569 The Entuit Secure Gastrointestinal Suture Anchor Set is intended for anchoring the anterior wall of the stomach to the abdominal wall prior to the introduction of interventional…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0959-2019·2019-03-06

    Shimadzu BRANSIST safire Digital Angiography System Software Recall

    Shimadzu Medical Systems is recalling eight BRANSIST safire digital angiography systems due to a software error that can cause abnormal termination during initial patient registration.

    Product
    BRANSIST safire Product Usage: DIGITAL ANGIOGRAPHY SYSTEM This system is intended to be used for radiologic visualization of the heart, blood vessels or lymphatic system during or after injection of a contrast medium. It is to be used in the diagnosis of the circulatory…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0968-2019·2019-03-06

    Cook Inc. Recalls Gastrointestinal Suture Anchor Sets Due to Retention Mechanism Issue

    Cook Inc. is recalling 975 Entuit Secure Gastrointestinal Suture Anchor Sets because a specific extension spring lot may cause difficulty sliding down the retention mechanism.

    Product
    Entuit Secure Gastrointestinal Suture Anchor Set, Catalog Number GIAS-SRM-3, Order Number G35570 The Entuit Secure Gastrointestinal Suture Anchor Set is intended for anchoring the anterior wall of the stomach to the abdominal wall prior to the introduction of interventional…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0960-2019·2019-03-06

    Abbott Vascular Recalls PLUS 30 Priority Pack Accessory Kit Due to Expiration Error

    Abbott Vascular is recalling 26 units of the PLUS 30 Priority Pack Accessory Kit because an incorrect expiration date was entered for one lot.

    Product
    PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended for use during vascular procedures in conjunction with interventional and / or diagnostic devices (e.g., balloon dilatation catheters, atherectomy devices, stent delivery systems, intravascular ultrasound…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0517-2019·2019-03-06

    Lupin Recalls Moxifloxacin Ophthalmic Solution Due to Impurity Levels

    Lupin Pharmaceuticals is recalling Moxifloxacin Ophthalmic Solution because impurity levels exceeded specifications. The recall covers 674,628 bottles distributed nationwide and in Puerto Rico.

    Product
    MOXIFLOXACIN — MOXIFLOXACIN (MOXIFLOXACIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0958-2019·2019-03-06

    Exactech Equinoxe Humeral Stem Recalled for Incorrect Packaging Instructions

    Exactech is recalling 40 Equinoxe Preserve Humeral Stems because they may have been packaged with instructions for a different knee implant.

    Product
    Equinoxe Preserve Humeral Stem, 8mm Product Usage: The Equinoxe Preserve Stems are indicated for use in skeletally mature individuals with degenerative diseases of the glenohumeral joint where anatomic total arthroplasty,anatomic hemi-arthroplasty,or reverse total…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V169000·2019-03-05

    Jayco Recalls 2017-2019 Seismic Fifth Wheel Trailers for Brake Line Defect

    Jayco is recalling 2017-2019 Seismic fifth wheel trailers with optional hydraulic brakes because brake lines may be pinched or cut, increasing crash risk.

    Product
    JAYCO — JAYCO, JAYCO FIFTH WHEEL redundant SEISMIC, SEISMIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V173000·2019-03-05

    Jayco Recalls 2019 Fifth Wheel Trailers Due to Awning Fuse Error

    Jayco is recalling 2019 North Point and Pinnacle fifth wheel trailers because an incorrect fuse in the awning circuit increases the risk of fire.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL PINNACLE, NORTH POINT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V175000·2019-03-05

    Entegra Esteem Motorhomes Recalled for Parking Brake Cable Defect

    Entegra is recalling 2019 Esteem motorhomes because parking brake cable ends may be too small, allowing the cable to disconnect and preventing the emergency brake from engaging.

    Product
    ENTEGRA — ENTEGRA ESTEEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V176000·2019-03-05

    Kenworth Trucks Recalled for Potential Rear Axle Oil Deficiency

    PACCAR is recalling 2020 Kenworth T680, T800, T880, W900, and W990 trucks because rear axles may lack oil, increasing crash risk.

    Product
    KENWORTH — KENWORTH T680, T800, T880, W900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V171000·2019-03-05

    2019 Western Star Trucks Recalled for Odometer Unit Labeling Error

    Daimler Trucks North America is recalling 2019 Western Star 4700 and 4900 trucks because the odometer displays miles but tracks kilometers, potentially causing driver confusion.

    Product
    WESTERN STAR — WESTERN STAR 4700, 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V170000·2019-03-05

    Thomas Built Buses Minotour Recalled for Wheelchair Lift Safety Defect

    Daimler Trucks North America is recalling 2003-2019 Thomas Built Buses Minotour school buses because the wheelchair lift can operate without the parking brake engaged, posing an injury risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide