The Recall Desk

State

American Samoa product recalls

73,106 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
5
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 5 (20%) are Severe.

Which agencies issued them

These figures cover only the 25 recalls whose distribution notice names American Samoa specifically. The 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12951–12975 of 73131

  • HighNHTSA·24V033000·2024-01-19

    Nova Bus Recalls 2017-2019 LFS Models for Door Window Marking Defect

    Nova Bus is recalling 2017-2019 LFS and LFS Artic buses because driver's door windows may have incorrect DOT code marks, potentially leading to improper glass replacement and reduced visibility.

    Product
    NOVA BUS — NOVA BUS LFS ARTIC, LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24084·2024-01-18

    Home Design Upholstered Low Profile Beds Recalled for Fall Injury Risk

    Home Design is recalling about 527,177 upholstered low-profile beds sold through Wayfair, Walmart.com, and Overstock.com from July 2018 through November 2023. The beds can break, sag, or collapse during use, creating a fall and injury hazard.

    Product
    Upholstered Low Profile Standard and Platform Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V021000·2024-01-18

    Lode King Trailers Recalled for Anti-Lock Brake System Defect

    Lode King is recalling specific AHV45-3 and Prestige trailers because reversed ABS sensor connections may reduce braking effectiveness during wheel lockup.

    Product
    LODE KING — LODE KING AHV45-3, PRESTIGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V026000·2024-01-18

    Navistar Recalls 2024 International HV and MV Trucks for Seat Belt Defect

    Navistar is recalling 2024 International HV and MV trucks because the driver's seat belt tether bolt may not be properly seated, increasing injury risk in a crash.

    Product
    INTERNATIONAL — INTERNATIONAL HV, MV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-01182024-02·2024-01-18

    USDA Issues Public Health Alert for Ready-to-Eat Charcuterie Products

    USDA FSIS issued a public health alert for Busseto and Fratelli Beretta charcuterie products due to possible Salmonella contamination linked to a multistate outbreak.

    Product
    Fratelli Beretta USA, INC. — FSIS Issues Public Health Alert for Ready-To-Eat Charcuterie Products Due to Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·24V027000·2024-01-18

    Navistar Recalls 2024 IC EV School Buses for Mislabeled Cables

    Navistar is recalling 2024 IC EV school buses because high-voltage cables may be mislabeled, posing an electrical shock risk to technicians.

    Product
    IC BUS — IC BUS EVSB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V023000·2024-01-18

    2018–2022 Land Rover Range Rover and Range Rover Sport rearview camera recall

    Jaguar Land Rover is recalling certain 2018–2022 Range Rover and Range Rover Sport vehicles because water may enter the rearview camera, causing it to fail to display or show a distorted image, reducing rear visibility while in reverse.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24085·2024-01-18

    Bokser Home 100% Cotton Mattress Pads Recalled for Fire Hazard

    Bokser Home is recalling about 2,300 units of 100% cotton mattress pads because they violate federal flammability regulations and pose a fire hazard. No injuries have been reported.

    Product
    Bokser Home 100% Cotton Mattress Pads
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-01182024-01·2024-01-18

    USDA Issues Public Health Alert for Uninspected Raw Frozen Pork Dumplings

    USDA FSIS issued a public health alert for raw frozen pork dumplings produced without federal inspection. No illnesses have been reported, but consumers are urged to discard the products.

    Product
    Dim Sum Factory, Inc. — FSIS Issues Public Health Alert for Raw Frozen Pork Dumpling Products Produced without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·24V025000·2024-01-18

    2023 and 2024 Kia Carnival vehicles recalled for loose roof molding

    Kia is recalling certain 2023–2024 Carnival and 2023–2024 Sportage vehicles because the roof molding may loosen and detach, creating a road hazard for other vehicles.

    Product
    KIA — KIA CARNIVAL, SPORTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24086·2024-01-18

    Steamist Wall-Mounted Tilt-Up Bath Shower Seats Recalled for Fall and Laceration Hazards

    Steamist is recalling about 3,900 wall-mounted, folding teak wood shower seats because the support rods and mounting brackets can corrode and break, creating fall and laceration hazards. The firm has received 62 reports of the seats breaking, including 4 injury reports.

    Product
    Tilt-Up Bath & Shower Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0220-2024·2024-01-17

    Prescription Vigabatrin Powder Recalled for Defective Container Leakage Risk

    InvaGen Pharmaceuticals recalls Vigabatrin for Oral Solution nationwide due to defective containers that may leak. Consumers with affected lot should contact their pharmacy or healthcare provider.

    Product
    VIGABATRIN — VIGABATRIN (VIGABATRIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V020000·2024-01-17

    Morgan Super 3 motorcycles recalled for brake master cylinder weld defect

    Morgan Motor Company is recalling 2023 Super 3 motorcycles because a defective weld may cause brake failure. Owners should contact the manufacturer for a free repair.

    Product
    MORGAN MOTOR COMPANY — MORGAN MOTOR COMPANY SUPER 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0691-2024·2024-01-17

    VISERA Cysto-Nephro Videoscope Model CYF-V2: Reusable Brush Cleaning Update

    Olympus is updating instructions for the VISERA Cysto-Nephro Videoscope (Model CYF-V2) nationwide, removing reusable brushes from manual cleaning procedures. Single-use brushes remain compatible.

    Product
    Model No. CYF-V2, VISERA Cysto-Nephro Videoscope
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0643-2024·2024-01-17

    Bard Mission Biopsy Instrument Kits Recalled for Improper Needle-Cannula Fit

    Bard is recalling Mission Disposable Core Biopsy Instrument Kits due to dimensional issues that may prevent the biopsy needle from fitting properly into the cannula, potentially causing tissue injury and prolonging procedures.

    Product
    Bard Mission Disposable Core Biopsy Instrument Kit (REF/Name): 1410MSK/ Mission Kit 14G x 10CM; 1416MSK/ Mission Kit 14G x 16CM; 1610MSK/ Mission Kit 16G x 10CM; 1616MSK/ Mission Kit 16G x 16CM; 1810MSK/ Mission Kit 18G x 10CM; 1816MSK/ Mission Kit 18G x 16CM; 1820MSK/ Mission…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0714-2024·2024-01-17

    Ambu aView 2 Monitor recalled for fire and burn hazard from oversized mounting screws

    Ambu is recalling the aView 2 A Monitor due to fire and burn hazards if mounting screws longer than 16mm are used. Improper installation can penetrate the lithium-ion battery, causing fires, severe burns, and smoke inhalation.

    Product
    Ambu aView 2 A Monitor, Catalog numbers 405011000 and 405011000US2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0697-2024·2024-01-17

    Olympus ENDOEYE HD II Videoscope Image Discoloration Recall

    Two Olympus ENDOEYE HD II Rigid Videoscope catalog numbers (WA50040A, WA50042A) have been recalled due to reports of pink or green image discoloration during use. The issue could require device exchange during surgery and potentially result in visual impacts or bleeding.

    Product
    Olympus ENDOEYE HD II Rigid Videoscope Catalog Numbers: WA50040A, WA50042A -used with a video system center, light source, documentation equipment, monitor, hand instruments, electrosurgical unit, and other ancillary equipment for endoscopy and endoscopic surgery within the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V018000·2024-01-17

    Heartland Recalls 2024 Corterra Fifth Wheels for Incorrect Tire Labels

    Heartland is recalling 2024 Corterra fifth wheels because certification labels may have missing or incorrect tire size information, potentially leading to the installation of wrong tires.

    Product
    HEARTLAND — HEARTLAND CORTERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0698-2024·2024-01-17

    Medtronic Percutaneous Surgical Pins Recalled Due to Potential Fitting Defects

    Medtronic is recalling 4,235 percutaneous surgical pins that may have a manufacturing defect preventing proper fit into or removal from the tap cap. The pins were distributed nationwide and internationally.

    Product
    Medtronic, REF 9733235, Pin, 100mm, STERILE, PERCUTANEOUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0677-2024·2024-01-17

    Philips BrightView Gamma Camera System Recalled for Extremity Entrapment Hazard

    Philips is recalling BrightView Gamma Camera Systems because a gap can form between patient support and detector during quality assurance scans, creating an extremity entrapment hazard that may cause fractures or crush injuries.

    Product
    BrightView, Gamma Camera System, Product Code 882480.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0640-2024·2024-01-17

    Philips Incisive CT Scanner Software Issues May Cause Misdiagnosis

    Philips is recalling Incisive CT scanners due to nine software defects including image artifacts, incorrect orientation labels, display failures, and positioning errors that could lead to misdiagnosis or need for rescans. No illnesses have been reported.

    Product
    Incisive CT, model 728143 & 728144 running Software Version 5.0.0.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0641-2024·2024-01-17

    Medical diagnostic reagent recall: incorrect cell staining fluorescence

    BD Biosciences is recalling CD11b APC diagnostic reagent vials that may produce dim fluorescence signals, potentially causing false negative results and misdiagnosis of blood cancers.

    Product
    CD11b APC: ASR, REF: 340936, and CE, REF: 333143
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0644-2024·2024-01-17

    Olympus ENDOEYE Videoscope Recalled for Reprocessing Instructions Deviations

    Olympus Corporation recalls 1,403 ENDOEYE Flex endoscopic videoscopes due to deviations in reprocessing instructions. Affected devices may not be reprocessed properly for safe reuse in surgical procedures.

    Product
    OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (5.4 mm diameter) Model: LTF-S190-5 Used with a video system center, light source, documentation equipment, monitor, hand instruments, electrosurgical unit, and other ancillary equipment for endoscopy and endoscopic surgery…
    Category
    Medical Device
    Distribution
    Distributed nationwide