The Recall Desk

State

American Samoa product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40326–40350 of 73831

  • SevereUSDA FSIS·002-2018·2018-01-05

    Crescent City Meats Recalls Underprocessed Ready-to-Eat Tasso Ham Products

    Crescent City Meats is recalling approximately 430 pounds of ready-to-eat Tasso Cajun Spicy Ham because the product may be underprocessed and undercooked.

    Product
    Crescent City Meats — Crescent City Meats Recalls Ready-To-Eat Tasso Ham Products due to Underprocessing
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·18077·2018-01-04

    HP Recalls Lithium-Ion Batteries for Notebook Computers and Mobile Workstations

    HP is recalling about 50,000 lithium-ion batteries for notebook computers and mobile workstations because they can overheat, posing fire and burn hazards.

    Product
    Lithium-ion batteries for HP notebook computers and mobile workstations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V004000·2018-01-04

    Audi Recalls Vehicles Due to Passenger Air Bag Inflator Explosion Risk

    Volkswagen Group of America is recalling specific Audi models because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.

    Product
    AUDI — AUDI S6, S4 CABRIOLET, A4 CABRIOLET, A6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V005000·2018-01-04

    Gulf Stream Recalls 2011-2012 Trailers Due to Fire Extinguisher Defect

    Gulf Stream is recalling 2011-2012 recreational trailers because the installed fire extinguishers may clog or detach, potentially failing to discharge or causing injury.

    Product
    GULF STREAM — GULF STREAM SERENITY, SKY, SPECIAL EDITION, RIDGELINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V006000·2018-01-04

    Altec Recalls 2010-2011 Knuckle Boom Cranes Due to Bearing Fastener Failure

    Altec Industries is recalling 2010-2011 Effer 440 and 470 Knuckle Boom Cranes because rotation bearing fasteners may fail, causing the pedestal to crack and increasing injury risk.

    Product
    ALTEC — ALTEC 470 KNUCKLE BOOM CRANE, EFFER 440
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18713·2018-01-04

    SureFit Recalls Riding Lawn Mower Blade Spindle Shafts Due to Impact Hazard

    SureFit is recalling about 900 riding lawn mower blade spindle shafts and assemblies because they can break and become projectiles, posing an impact injury risk.

    Product
    SureFit™ riding lawn mower blade spindle shafts and assemblies
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0213-2018·2018-01-03

    Sterilmed recalls reprocessed St. Jude Medical Agilis NxT Steerable Introducers

    Sterilmed Inc is recalling 112 reprocessed St. Jude Medical Agilis NxT Steerable Introducers due to inadequate seals caused by missing adhesive glue.

    Product
    St. Jude Medical. Agilis NxT Steerable Introducer: B1-Directional, Medium Curl 22.4 mm, 71 cm, 6.5 F ID; Dilator: 94 cm, 8.5 F; Super Stiff, Guidewire: 180 cm, 0.032". Reprocessed device for single use only, sterile. Product Usage: The reprocessed steerable introducer…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V003000·2018-01-03

    Forest River Recalls 2018 Glaval Legacy Buses for Brake Caliper Defect

    Forest River is recalling 2018 Glaval Legacy buses because improperly tightened brake caliper bolts may cause the calipers to detach, reducing braking power and increasing crash risk.

    Product
    GLAVAL BUS — GLAVAL BUS LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0270-2018·2018-01-03

    L3 Security Cabinet X-ray System Recalled for Shielding Gaps

    L3 Security & Detection is recalling 471 Examiner 3DX 6000 cabinet X-ray systems used for airline baggage screening due to shielding gaps that may cause excessive X-ray emissions.

    Product
    L3 Security & Detection System Cabinet X-ray system used for security screening of checked airline baggage.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0292-2018·2018-01-03

    Philips IntelliVue Patient Monitors Recalled for Distorted ST-Segment Display

    Philips is recalling specific IntelliVue patient monitors and measurement servers because they may display distorted ST-segments during 12-lead ECG monitoring.

    Product
    IntelliVue Multi Measurement Server, IntelliVue Multi Measurement Server SLCP, IntelliVue Multi Measurement Server X2, IntelliVue Patient Monitor Models MP2 and MP5 Product Usage: Indicated for use by health care professionals whenever there is a need for monitoring the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0295-2018·2018-01-03

    Medline Recalls Sterile Elastic Esmark Bandages Due to Sterilization Failure

    Medline Industries is recalling 5,722 units of sterile elastic bandages because they may not have been properly sterilized.

    Product
    Sterile Elastic Esmark Bandage, 3" x 9", individually packaged in a Tyvek plastic form fill seal pouch and placed into a corrugate case, 20 individually packed bandages per case.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0290-2018·2018-01-03

    Remel Shigella sonnei Agglutinating Serum Recalled for Failure to Agglutinate

    Remel Inc is recalling Shigella sonnei Agglutinating Serum because it may fail to agglutinate within the specified minimum reaction time.

    Product
    Remel Shigella sonnei Phase 1 & 2 Agglutinating Serum, Ref R30164201 ZH01. Product Usage: Suitable for the use in slide agglutination tests to identify Shigella cultures presumptively for epidemiological and diagnostic purposes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0130-2018·2018-01-03

    Pharmedium Recalls Morphine Sulfate Injection Due to Labeling Errors

    Pharmedium Services LLC is recalling morphine sulfate injection due to incorrect or missing lot and expiration dates on the labels.

    Product
    morphine Sulfate in 0.9% Sodium Chloride Injection 2 mL Total Volume 1 mg per mL (2 mg per 2 mL), For IV Use, Rx Only, Compounded by: PharMEDium Services LLC. 913 N Davis Ave Cleveland, MS 38732, NDC# 61553-259-28
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0132-2018·2018-01-03

    Pharmedium Recalls Hydromorphone Injection Due to Labeling Errors

    Pharmedium Services LLC is recalling Hydromorphone HCl Injection due to incorrect or missing lot and expiration dates.

    Product
    HYDROmorphone HCl in 0.9% Sodium Chloride Injection, 1 mL Total Volume 1 mg per mL, For IV Use Only, Rx Only, Compounded by: PharMEDium Services LLC. 913 N Davis Ave Cleveland, MS 38732, NDC# 61553-165-78
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0131-2018·2018-01-03

    Pharmedium Recalls Morphine Sulfate Injection Due to Labeling Errors

    Pharmedium Services LLC is recalling specific lots of compounded morphine sulfate injection because the labels may have incorrect or missing lot and expiration dates.

    Product
    morphine Sulfate in 0.9% Sodium Chloride Injection 1 mL Total Volume 2 mg per mL , For IV Use, Rx Only, Compounded by: PharMEDium Services LLC. 913 N Davis Ave Cleveland, MS 38732, NDC# 61553-455-78
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0133-2018·2018-01-03

    Auryxia Ferric Citrate Tablets Recalled for Damaged Desiccant Packets

    Keryx Biopharmaceuticals is recalling Auryxia (ferric citrate) tablets because damaged silica gel packets may allow desiccant granules to contact the medication.

    Product
    AURYXIA — AURYXIA (FERRIC CITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18E003000·2018-01-02

    Takata Frontal Passenger Air Bag Inflator Recall for 2009 Vehicles

    Takata is recalling specific 2009 model year air bag inflators that may explode due to propellant degradation. This affects vehicles registered in 22 specific states.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18E002000·2018-01-02

    Takata Frontal Passenger Air Bag Inflator Recall for 2010 Vehicles

    Takata is recalling specific frontal passenger air bag inflators in 2010 vehicles registered in 22 states and D.C. due to a risk of explosion causing serious injury or death.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V002000·2018-01-02

    Forest River Recalls 2018 Surveyor Trailers Due to Fire Risk

    Forest River is recalling 2018 Surveyor recreational trailers because an incorrect circuit breaker can cause wiring to melt, increasing the risk of a fire.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E001000·2018-01-02

    Takata Frontal Passenger Air Bag Inflator Recall for 2013 Vehicles

    Takata is recalling specific 2013 model year air bag inflators in 13 states and territories due to a risk of explosion from propellant degradation.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18076·2018-01-02

    Comfort Research Recalls Ultra Lounge Bean Bag Chair Covers

    Comfort Research is recalling about 1,200 Ultra Lounge bean bag chair covers due to risks of entrapment and suffocation to children.

    Product
    Ultra Lounge bean bag chair covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V001000·2018-01-02

    Erwin Hymer Recalls Motorhomes With Defective Fire Extinguishers

    Erwin Hymer is recalling 2012-2018 motorhomes because the installed fire extinguishers may clog and fail to discharge properly.

    Product
    ROADTREK — ROADTREK, CARADO, SUNLIGHT ZION, RS ADVENTUROUS, BANFF, AXION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V847000·2017-12-29

    ShowHauler Recalls 2003-2018 Motorhomes Due to Fire Extinguisher Defect

    ShowHauler is recalling 2003-2018 Garage Coach, Toter Coach, and Motorhome vehicles because their fire extinguishers may clog or detach, posing injury risks during a fire.

    Product
    SHOWHAULER — SHOWHAULER GARAGE COACH, TOTER COACH, MOTORHOME
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V846000·2017-12-28

    Forest River Recalls 2017-2018 Georgetown RVs for Brake Defect

    Forest River is recalling 2017-2018 Georgetown recreational vehicles because missing plugs in the brake system may cause fluid leaks or air ingestion, increasing stopping distance.

    Product
    FOREST RIVER — FOREST RIVER GEORGETOWN
    Category
    Vehicle
    Distribution
    Distributed nationwide