The Recall Desk

State

American Samoa product recalls

73,218 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 73,218 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

16901–16925 of 73243

  • SevereNHTSA·23V137000·2023-03-02

    Land Rover Recalls 2023 Defender 130 for Third-Row Seat Latch Defect

    Jaguar Land Rover is recalling 2023 Defender 130 vehicles with third-row seats because the seatback latch may not secure child seat tethers properly, increasing crash injury risk.

    Product
    LAND ROVER — LAND ROVER DEFENDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23730·2023-03-02

    Multi-Purpose Kids Bike Helmets Recalled for Head Injury Risk

    Ouwoer Kids Bike Helmets sold on Amazon from March to November 2022 fail to meet federal safety standards and may not protect children in a crash. About 120 units are affected; no injuries have been reported.

    Product
    Multi-Purpose Kids Bike Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23138·2023-03-02

    Patagonia Infant Capilene Base Layer Sets Recalled for Choking Hazard

    Patagonia is recalling about 8,000 Infant Capilene Midweight Base Layer Sets because snaps on the bodysuit can detach, posing a choking hazard to infants. One incident of a snap detaching and being mouthed by a baby has been reported.

    Product
    Infant Capilene Midweight Base Layer Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V138000·2023-03-02

    Newmar Motorhome Entry Door Latch May Fail, Preventing Emergency Exit

    Newmar is recalling certain 2021-2023 Bay Star, Bay Star Sport, and Canyon Star motorhomes because the entry door latch may fail and prevent entry or exit, increasing the risk of injury in emergencies.

    Product
    NEWMAR — NEWMAR BAY STAR, CANYON STAR, BAY STAR SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23140·2023-03-02

    RELiON InSight Series Lithium Batteries Recalled for Thermal Burn and Fire Risk

    RELiON Battery is recalling certain lots of InSight Series 48V lithium-ion batteries because they can overheat, posing thermal burn and fire hazards. The company has received five reports of overheating with no injuries reported to date.

    Product
    RELiON InSight Series® lithium batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V140000·2023-03-02

    2023 Winnebago Adventurer, Vista, Sunstar motorhomes recalled for missing rear reflectors

    Winnebago is recalling certain 2023 Adventurer, Vista, and Itasca Sunstar motorhomes for missing rear reflectors that fail federal safety standards. Missing reflectors reduce visibility to other drivers, increasing crash risk.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA VISTA, ADVENTURER, SUNSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V139000·2023-03-02

    Off Grid Trailers Recalls 150 Units Due to Gas Leak Risk

    Off Grid Trailers is recalling 150 Expedition, Switchback, and Pando travel trailers because a cooktop component may fracture and cause a gas leak.

    Product
    OFF GRID TRAILERS — OFF GRID TRAILERS EXPEDITION, SWITCHBACK, PANDO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23731·2023-03-02

    Classic Whimsy Children's Pajamas Recalled for Flammability Standard Violation

    Smocked Runway is recalling about 7,200 Classic Whimsy children's pajamas that fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries. Consumers should stop using the product immediately and contact the manufacturer for return instructions.

    Product
    Classic Whimsy children's pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23139·2023-03-02

    Primark Children's Bamboo Plates Recalled for Lead and Formaldehyde

    Primark is recalling about 1,665 children's bamboo plates sold from October 2021 through August 2022 because they contain elevated levels of lead and formaldehyde, which are toxic if ingested by children.

    Product
    Children's Bamboo Plates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23137·2023-03-02

    TJX Office Chairs Recalled Due to Fall Hazard

    The TJX Companies is recalling approximately 81,700 office chairs because the back can break or detach from the seat base when occupied, posing a fall hazard. The firm has received 12 reports of the chair back failing, including 10 reports of injuries.

    Product
    Office Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23141·2023-03-02

    Helly Hansen Adult Workwear Sweatshirts and Hoodies Recalled for Burn Hazard

    Helly Hansen is recalling about 13,900 adult workwear sweatshirts and hoodies because they fail to meet federal flammability standards for clothing textiles, posing a risk of burn injuries.

    Product
    Adult workwear sweatshirts and hoodies
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23733·2023-03-02

    CTRL Imperial Wakeboard Bindings Recalled Due to Fall Hazard

    Active Sports is recalling CTRL Imperial Wakeboard Bindings because the binding can partially detach from the baseplate or the external mount can crack, causing users to lose balance and fall into the water. The company has received 21 reports of detachment or cracking but no injuries have been reported.

    Product
    CTRL Imperial Wakeboard Bindings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23732·2023-03-02

    DR Power PRO XL501 Chipper Shredders Recalled for Laceration Hazard

    DR Power is recalling about 2,100 PRO XL501 Chipper Shredders because the fin scroll can fail and eject metal pieces from the hopper during operation. No injuries have been reported, but the company has received six reports of metal ejection.

    Product
    DR®Power PRO XL501 Chipper Shredders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateNHTSA·23T001000·2023-03-02

    Continental Recalls Tires with Missing Identification Markings

    Continental Tire is recalling specific General Altimax RT43 tires because they lack required identification markings, which could hinder future recall efforts.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1137-2023·2023-03-01

    NovaStar TS Anti-Asphyxia Valve recalled for magnetic interference risk

    Draeger Medical recalls NovaStar TS Anti-Asphyxia Valves due to magnets that may interfere with implanted and non-implanted medical devices and metallic implants.

    Product
    NovaStar TS, Anti-Asphyxia Valve, Reusable, Material Numbers MP01576 (Size S), MP01577 (Size M), and MP01578 (Size L)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1138-2023·2023-03-01

    FDA Recalls NovaStar TS Standard Elbow Reusable Components for Magnet Interference Risk

    Draeger Medical is recalling 893 units of NovaStar TS Standard elbow components due to magnets that could interfere with medical devices and metallic implants.

    Product
    NovaStar TS, Standard elbow, Reusable, Material Numbers MP01579 (Size S), MP01580 (Size M), and MP01581 (Size L)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V133000·2023-03-01

    Coachmen Motorhomes Recalled for Entry Door Latch Failure

    Forest River is recalling 2013 Coachmen Cross Country and 2023 Coachmen Sportscoach motorhomes because the entry door latch may fail, preventing entry or exit.

    Product
    COACHMEN — COACHMEN SPORTSCOACH, CROSS COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0348-2023·2023-03-01

    Warfarin Sodium Tablets Recalled Due to Failed Impurity and Degradation Specifications

    Rising Pharmaceuticals is recalling Warfarin Sodium Tablets USP 1 mg due to failed impurities and degradation specifications. Approximately 12,216 bottles may have been distributed nationwide.

    Product
    Warfarin Sodium Tablets, USP 1 mg, 100-count bottle, Rx Only, Distributed by: Rising Health, LLC, Saddle Brook, NJ 07663, NDC# 57237-119-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1166-2023·2023-03-01

    Diagnostic Imaging System Recalled for Potential Ceiling and Wall Collision Risk

    Siemens Luminos dRF diagnostic imaging system is being recalled nationwide due to potential collision with ceilings, walls, or objects caused by default room configuration parameters. Collisions could result in serious injury to patients or staff.

    Product
    Luminos dRF with software VD10- A diagnostic imaging system for radiographic and fluoroscopic studies Model Number: 10094200
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1167-2023·2023-03-01

    Diagnostic imaging system recalled for collision risk from default settings

    Siemens Luminos dRF Max diagnostic imaging systems are being recalled due to a risk of collision with ceiling, walls, or nearby objects caused by default room configuration settings. This could result in serious injury to staff or patients.

    Product
    Luminos dRF Max with software VE10, VF10, VF11- A diagnostic imaging system for radiographic and fluoroscopic studie Model Number:10762471
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1159-2023·2023-03-01

    IV Start Kit Recalled Due to Connector Manufacturing Defect

    Cardinal Health Presource Packs IV start kits with ICU MicroClave Clear Connectors are being recalled due to a manufacturing defect that may cause fluid leaks and loss of fluid path integrity.

    Product
    Cardinal Health Presource Packs IV START KIT-Intended for IV Access CATALOG #: 01A4553E
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1156-2023·2023-03-01

    HydroMID 4Fr Peripheral Venous Catheter Kit Recalled for Incorrect Component Labeling

    Access Vascular is recalling HydroMID 4Fr Single Lumen Maximal Barrier Kits due to an incorrect component listed on the inner kit label. The error could lead to confusion and improper use of the device.

    Product
    HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term access (<30days) to the peripheral venous access system for intravenous therapy Product Number: 80004004
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0339-2023·2023-03-01

    Levothyroxine sodium oral solution recalled due to subpotency

    IBSA Pharma Inc. has recalled TIROSINT levothyroxine sodium oral solution nationwide due to subpotency. Some doses may contain less active ingredient than labeled. Patients should contact their healthcare provider.

    Product
    TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1163-2023·2023-03-01

    Medline Sterile Hand Pack recalled for inadequate sterilization

    Medline Sterile Hand Pack surgical prep kits are recalled because components were improperly placed in the nonsterile portion of the tray and did not receive proper sterilization. Affects 1,689 trays distributed in AR, CO, and GA.

    Product
    (1) Medline Sterile Hand Pack, Item DYNJ63380A, 3 kits per case, contains BD Chloraprep Hi-Lite Orange, 26 mL Applicator, Vendor PN: 930815NS; and (2) Medline Sterile Hand Pack, Item DYNJ63380C, 3 kits per case, contains BD Chloraprep Hi-Lite Orange, 26 mL Applicator, Vendor…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1168-2023·2023-03-01

    Diagnostic imaging system recalled due to ceiling and wall collision risk

    Siemens Uroskop Omnia Max imaging systems are recalled due to collision risk with ceilings, walls, or objects caused by default configuration settings. The systems may move dangerously, potentially injuring staff or patients.

    Product
    Uroskop Omnia Max with software VE10 & VF11- A diagnostic imaging system for radiographic and fluoroscopic studie Model Number:10762473
    Category
    Medical Device
    Distribution
    Distributed nationwide