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.

13326–13350 of 73131

  • HighFDA (Devices)·Z-0430-2024·2023-12-13

    ProCuity Hospital Patient Beds Recalled for Missing Electrical Safety Testing

    Stryker is recalling ProCuity bed series model 3009 because they are missing electrical safety test values, presenting a risk of tissue burn or electrical shock to patients.

    Product
    ProCuity bed series, model number 3009, item number: 3009PX-LEX-450.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0142-2024·2023-12-13

    Children's Acetaminophen Suspension Recalled for Failed Impurity Specifications

    KinderFarms is recalling KinderMed KIDS' PAIN & FEVER Acetaminophen oral suspension nationwide due to failed impurity and degradation specifications that do not meet FDA standards.

    Product
    PAIN AND FEVER — PAIN AND FEVER (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0497-2024·2023-12-13

    Integra Cranial Access Kit recalled over outer packaging defect

    Integra LifeSciences recalled the Integra Cranial Access Kit (160 units) due to a defect in the outer packaging that can split and compromise device sterility, creating an infection risk for neurosurgical procedures.

    Product
    Integra¿ Cranial Access Kit-For access to the subarachnoid space or the lateral ventricles of the brain. Catalog Number: HITHSP06
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0428-2024·2023-12-13

    ProCuity Patient Beds Recalled Missing Electrical Safety Test Values

    Stryker is recalling ProCuity patient beds (model 3009) for missing required electrical safety test documentation, creating a risk of electrical shock or tissue burn.

    Product
    ProCuity bed series, model number 3009, item number: 3009PX-LE-450.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0434-2024·2023-12-13

    ProCurity patient beds recalled for electrical safety testing defects

    Stryker is recalling ProCurity bed series (model 3009) due to missing electrical safety test values that could pose risk of electrical shock or tissue burn. Affected units were distributed nationwide and internationally.

    Product
    ProCurity bed series, model number 3009, item number: 3009PX-ZMX-450.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0137-2024·2023-12-13

    Bupropion Hydrochloride Extended-Release Tablets Recalled for Failed Dissolution

    Sun Pharmaceutical is recalling Bupropion Hydrochloride Extended-Release Tablets 200 mg due to failed dissolution specifications. The recall affects 2,016 bottles with lot HAD0630A distributed nationwide.

    Product
    BUPROPION HYDROCHLORIDE — BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0506-2024·2023-12-13

    TENS Devices Recalled for Missing Instruction Manual Warnings

    Liberty Medical Solutions is recalling 473 Multi-Mode TENS stimulator units distributed in five states due to missing warnings and contraindications in instruction manuals.

    Product
    Multi-Mode Stimulator, Transcutaneous Electrical Nerve Stimulation
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0140-2024·2023-12-13

    LET Gel Topical Anesthetic Recalled Due to Incorrect Product Formulation

    Right Value Drug Stores is recalling LET Gel topical anesthetic syringes nationwide due to incorrect product formulation. Patients should not use affected syringes and should consult their healthcare provider.

    Product
    LET Gel (Lidocaine HCL/Epinephrine Bitartrate/Tetracaine HCL 4%/0.18%/0.5% Topical Gel), Single-use Topical Syringe, 3mL syringe, 10/pack, Rx only, Carie Boyd Pharmaceuticals, 8400 Esters Blvd, Ste# 190, Irving, TX 75063, NDC73271-1003-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0451-2024·2023-12-13

    Blood Culture Identification Panel Quality Control Test Reporting Issue

    BioFire Diagnostics is recalling BIOFIRE Blood Culture Identification 2 (BCID2) Panels due to instrument characteristic changes that cause Candida tropicalis to be detected but reported as 'Not Detected' in quality control testing.

    Product
    BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, used with Maine Molecular Quality Controls, Inc (MMQCI) FilmArray BCID2 Control Panel M416, which is referenced in Quality Control Materials for use with BIOFIRE FILMARRAY and BIOFIRE SPOTFIRE Panels…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0500-2024·2023-12-13

    Luminex VERIGENE BC-GP Utility Trays Recalled Due to Potential Defects

    Luminex Corporation is recalling 222 kits (4,440 VERIGENE BC-GP Utility Trays) used in blood culture testing due to potentially defective utility trays. The affected lot (062123018C) expires December 20, 2023.

    Product
    Luminex VERIGENE BC-GP Utility Tray (5-Pack Carrier), Gram-Positive Blood Culture Nucleic Acid Test, REF 20-011-018, a component of the Luminex VERIGENE BC-GP Utility Kit, REF 20-012-018, containing 20 tests.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V838000·2023-12-12

    Tesla Model Y Autosteer Recall: Software Update for Control Prominence

    Tesla is recalling 2.03 million 2012-2023 Model S/X/3/Y vehicles with Autosteer due to insufficient control prominence that may allow driver misuse and crash risk. A free OTA software update will be provided.

    Product
    TESLA — TESLA MODEL S, MODEL X, MODEL 3, MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V837000·2023-12-12

    Mazda Recalls B-Series Trucks for Incorrect Air Bag Installation

    Mazda is recalling 2004-2006 B-Series trucks because previously replaced front passenger air bag inflators may have been installed incorrectly, potentially preventing proper inflation during a crash.

    Product
    MAZDA — MAZDA B-SERIES TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V833000·2023-12-08

    American Coach American Eagle Motorhomes Recalled for Deflector Bracket Defect

    REV Recreation Group is recalling 2016-2023 American Coach American Eagle motorhomes because turbulence may loosen or break the rear air deflector mounting bracket hardware.

    Product
    AMERICAN COACH — AMERICAN COACH AMERICAN EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V836000·2023-12-08

    2023 Harley-Davidson FLHXSE Motorcycles Engine Control Software Defect

    Harley-Davidson is recalling certain 2023 FLHXSE motorcycles due to an engine control module software defect that may cause loss of control at high speeds, increasing crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHXSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V835000·2023-12-08

    Mercedes-Benz Recalls 2021-2022 GLE Models Due to Fire Risk

    Mercedes-Benz is recalling 2021-2022 GLE 350 and GLE 450 vehicles because a 12-volt ground connection may overheat, increasing the risk of a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 450, GLE 350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V834000·2023-12-08

    Forest River Recalls 2024 XLR Boost Toy Haulers for Taillight Defect

    Forest River is recalling 2024 XLR Boost toy haulers because taillights may be insufficiently reflective, reducing visibility and increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER XLR BOOST TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·062-2023·2023-12-07

    Wayne Farms Recalls Undercooked Ready-to-Eat Chicken Breast Products

    Wayne Farms is recalling approximately 1,377 pounds of ready-to-eat chicken breast products that may be undercooked. The recall was initiated after a customer complaint regarding product appearance.

    Product
    Wayne Farms LLC — Wayne Farms, LLC, Recalls Ready-to-Eat Chicken Breast Products That May Be Undercooked
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V823000·2023-12-07

    Pierce Recalls 2019-2023 Tower Trucks Due to Wiring Harness Defect

    Pierce is recalling 2019-2023 Arrow XT, Enforcer, and Velocity tower trucks because a wiring harness may not be secured, risking basket tipping and injury.

    Product
    PIERCE — PIERCE ARROW XT, ENFORCER, VELOCITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24048·2023-12-07

    XpressGoods recalls magnetic balls for federal toy safety violations

    XpressGoods is recalling colorful neodymium magnetic balls that exceed federal safety limits for toy magnets. When swallowed, the magnets can lodge in the digestive system and cause serious injury or death.

    Product
    Colorful Metal Neodymium Magic Magnetic Balls - 8 color, 5mm
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V822000·2023-12-07

    Dutchmen Coleman Travel Trailers Recalled for Underrated Suspension Springs

    Keystone RV is recalling 2021-2022 Dutchmen Coleman travel trailers with suspension springs rated at 4400 pounds instead of 5100 pounds. The underrated springs can become overloaded, increasing crash risk.

    Product
    DUTCHMEN — DUTCHMEN COLEMAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24727·2023-12-07

    2022 Fugleman UT10E and UT10X Utility-Terrain Vehicles Fire Hazard Recall

    Segway Powersports is recalling about 1,100 2022 Fugleman UT10E and UT10X Utility-Terrain Vehicles because the ignition coil can fail, allowing fuel to enter the exhaust pipe and ignite, creating a fire hazard. One vehicle fire with property damage has been reported.

    Product
    2022 Fugleman UT10E and UT10X Utility-Terrain Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24040·2023-12-07

    SABRE Aim & Fire Pepper Gel Spray Canisters Failure to Deploy

    Security Equipment Corporation is recalling about 4,000 SABRE Aim & Fire Pepper Gel Spray canisters with expiration date 9/2027 because they lack a red nozzle needed to deploy the spray and will not function in an emergency. No injuries have been reported.

    Product
    SABRE Aim & Fire Pepper Gel Spray with Training Canisters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24042·2023-12-07

    Mary Meyer Bubba Bull Plush Toys Recalled for Choking Hazard

    Mary Meyer is recalling about 1,950 Bubba Bull Plush Toys because the eyes can break off and pose a choking hazard to young children. No injuries have been reported.

    Product
    Bubba Bull Plush Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide