The Recall Desk

State

American Samoa product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42476–42500 of 73834

  • LowFDA (Drugs)·D-0933-2017·2017-07-12

    PharMEDium Recalls Ropivacaine Pumps Due to Incorrect Lot and Expiration Dates

    PharMEDium Services, LLC is recalling 10 Ropivacaine HCl 0.2% ON-Q pumps nationwide due to incorrect or missing lot and expiration dates.

    Product
    Ropivacaine HCl 0.2% 750 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 600 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-279-33
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalNHTSA·17E034000·2017-07-10

    Takata Driver Frontal Air Bag Inflator Recall for Rupture Risk

    Takata is recalling specific driver-side air bag inflators that may rupture due to propellant degradation, posing a risk of serious injury or death.

    Product
    AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V435000·2017-07-10

    Chrysler Recalls 2011-2014 Vehicles for Alternator Failure Risk

    Chrysler is recalling specific 2011-2014 Dodge, Chrysler, and Jeep vehicles because the alternator may fail, causing the vehicle to stall or catch fire.

    Product
    DODGE — DODGE, CHRYSLER, JEEP DURANGO, 300, CHARGER, CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V437000·2017-07-10

    GM Recalls 40,683 Vehicles for Air Bag and Seat Belt Software Defect

    General Motors is recalling 40,683 vehicles from 2014-2017 because a software error may prevent front air bags and seat belt pretensioners from deploying in a crash.

    Product
    CHEVROLET — CHEVROLET, GMC, BUICK CORVETTE, SILVERADO 1500, SIERRA 1500, LACROSSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V438000·2017-07-10

    BMW Recalls 2014-2017 R1200GS Motorcycles for Fork Tube Separation Risk

    BMW is recalling 2014-2017 R1200GS and R1200GS Adventure motorcycles because the fixed fork tube may separate from the seal plug, increasing crash risk.

    Product
    BMW — BMW R1200 GS ADVENTURE, R 1200 GS ADVENTURE, R1200 GS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17E036000·2017-07-10

    MORryde Recalls Jerry Can Holders for Detachment Risk

    MORryde is recalling Jerry Can holders that may tear apart from the spare tire mount, creating a road hazard.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V434000·2017-07-07

    Chrysler Recalls 2017 Ram 1500 Trucks for Fuel Tank Valve Defect

    Chrysler is recalling 2017 Ram 1500 trucks because a broken fuel tank control valve may leak fuel if the vehicle is inverted, increasing fire risk in a rollover crash.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V431000·2017-07-07

    2017 Dodge Challenger Recall for Transmission Park Position Defect

    Chrysler is recalling 2017 Dodge Challengers with 5.7L V8 engines and eight-speed automatic transmissions because the vehicle may not stay in Park, increasing crash risk.

    Product
    DODGE — DODGE CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V432000·2017-07-07

    Dodge Journey Recall for Frontal Air Bag Wiring Defect

    Chrysler is recalling 2011-2015 Dodge Journey vehicles because the driver's frontal air bag wiring may chafe and short circuit, causing unexpected deployment.

    Product
    DODGE — DODGE JOURNEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V433000·2017-07-07

    2017 Jeep Compass Recall for Incorrect Jump Start Instructions

    Chrysler is recalling 2017 Jeep Compass vehicles because the User's Guide contains reversed battery terminal polarity for jump starting, which may increase the risk of injury.

    Product
    JEEP — JEEP COMPASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V430000·2017-07-06

    Forest River Recalls Transit Buses Due to Driveshaft Coupling Failure Risk

    Forest River is recalling specific 2015-2018 transit buses and work trucks because a flexible coupling may fail, potentially damaging brake and fuel lines.

    Product
    STARCRAFT — STARCRAFT, FOREST RIVER, GLAVAL PRODIGY BUS, STARLITE, CANDIDATE II, CROSSFIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V427000·2017-07-06

    Ford Recalls 2017 Edge, Fusion, and Lincoln MKZ for Torque Converter Defect

    Ford is recalling 2017 Edge, Fusion, and Lincoln MKZ vehicles with 2.0L engines and six-speed automatics because torque converter weld studs may be inadequate, risking loss of vehicle movement.

    Product
    LINCOLN — LINCOLN, FORD MKZ, FUSION, EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V428000·2017-07-06

    BMW Recalls 2006 Models for Front Passenger Air Bag Sensor Defect

    BMW is recalling 2006 3 and 5 Series vehicles because the front passenger seat occupant detection mat may crack, potentially deactivating the air bag in a crash.

    Product
    BMW — BMW 330XI, 325I, 530XI, 550I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E033000·2017-07-05

    Cummins Recalls L9 Diesel Engines in Pierce Fire Trucks

    Cummins is recalling L9 heavy-duty diesel engines installed in Pierce fire trucks because improperly tightened capscrews may cause the flexplate to separate, potentially leading to engine stalling and a crash.

    Product
    ENGINE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17184·2017-07-05

    Home Depot Recalls Crystal Chandeliers Due to Fire and Burn Hazards

    Home Depot is recalling Hampton Bay and Home Decorators Collection crystal chandeliers because halogen bulbs can melt parts, posing fire and burn risks.

    Product
    Crystal chandeliers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2639-2017·2017-07-05

    DeRoyal Dolphin Inflation Device Recalled for Sterility Assurance Defect

    DeRoyal Industries is recalling 426 Dolphin Inflation Devices due to a primary packaging defect that may compromise sterility.

    Product
    DeRoyal(R) Dolphin Inflation Device, REF 0185ND, Rx Only, STERILE EO, Dolphin is an inflation device indicated during angioplasty procedures to inflate and deflate the balloon catheter, and control pressure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0929-2017·2017-07-05

    Allergan Recalls Blephamide Ophthalmic Ointment Due to Impurity Failures

    Allergan is recalling 648 units of Blephamide ophthalmic ointment because stability testing showed impurities exceeding specifications.

    Product
    Blephamide (sulfacetamide sodium and prednisolone acetate ophthalmic ointment, USP) 10%/0.2% sterile, 3.5 g tube, RX only, Manufactured by Allergan, Irvine, California, 92612, U.S.A., NDC: 0023-0313-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2629-2017·2017-07-05

    Olympus Recalls High Frequency Resection Electrodes Due to Wire Breakage

    Olympus Corporation of the Americas is recalling 1,264 High Frequency Resection Electrodes because loop wires may break at the distal end.

    Product
    High Frequency Resection Electrodes, endoscope, ac-powered and accessories The electrodes are used for endoscopic diagnosis and treatment in urological and gynecological applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2653-2017·2017-07-05

    Shimadzu Ceiling X-ray Tube Support Recalled for Potential Cracks

    Shimadzu Medical Systems is recalling ceiling-type X-ray tube supports because cracks may develop on the tube holding shaft, posing a risk of equipment failure.

    Product
    SHIMADZU Ceiling Type X-ray Tube Support CH-200/CH-200M Catalog Number: CH-200/CH-200M Holds an x-ray tube unit and collimator combined with an z-ray high voltage generator, radiographic stand, and table. It is designed to perform radiography of patients either in a standing or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2640-2017·2017-07-05

    Merge Healthcare Recalls SpO2 Cables for Hemodynamics Monitors

    Merge Healthcare is recalling 219 SpO2 connecting cables for its Hemodynamics monitors because they may stop displaying patient SpO2 readings, causing a slight delay in patient care.

    Product
    SpO2 connecting cable for Masimo LNCS sensor (Merge Part Number: HW-HEMO-00014), Product Usage: Merge Hemodynamics monitors, measures, and records physiologic data from a human patient undergoing a cardiac catheterization procedure. The Monitoring System is for the…
    Category
    Medical Device
    Distribution
    Distributed nationwide