The Recall Desk

State

American Samoa product recalls

73,716 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 73,716 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30051–30075 of 73741

  • ModerateFDA (Devices)·Z-1227-2020·2020-02-19

    CooperVision Vertex Toric Contact Lenses Recalled for Incorrect Power

    CooperVision is recalling 216 units of Vertex Toric contact lenses because they have an incorrect power than expected.

    Product
    Coopervision Vertex Toric /2 Clear Toric- Power -2.50 -0.75 /90 Soft (hydrophilic) Contact Lens (extended wear)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0843-2020·2020-02-19

    Par Pharmaceutical Recalls Frovatriptan Tablets Due to Incorrect Expiration Date

    Par Pharmaceutical is recalling 9,936 cartons of Frovatriptan Succinate Tablets, 2.5mg, because they are labeled with an incorrect expiration date.

    Product
    Frovatriptan Succinate Tablets, 2.5mg, packaged in 1 blister card of 9 tablets per carton, Rx Only, Manufactured by: Almac Pharma Services Limited, Craigavon, BT63 5UA, UK; Manufactured for: Par Pharmaceutical, Chestnut Ridge, NY 10977, NDC 0603-3718-34.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V091000·2020-02-17

    Jayco Recalls Fifth Wheel Trailers Due to Underrated Axles

    Jayco is recalling 2013-2015 Fifth Wheel Seismic and 2015 Pinnacle trailers because they were built with 6,000lb axles instead of the intended 7,000lb axles.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL, JAYCO SEISMIC, PINNACLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V090000·2020-02-14

    Mercedes-Benz Recalls G 550 and AMG G63 for Stability Control Defect

    Mercedes-Benz is recalling 2019-2020 G 550 and AMG G63 vehicles because a faulty electrical resistor may deactivate Electronic Stability Program and Anti-lock Brake System.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ G 550, AMG G63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V088000·2020-02-14

    Kia Recalls Sedona and Sorento Models for ABS Module Fire Risk

    Kia is recalling 2006-2010 Sedona and 2007-2009 Sorento vehicles because moisture in the ABS module can cause an electrical short and engine compartment fire.

    Product
    KIA — KIA SEDONA, SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V089000·2020-02-14

    Mercedes-Benz Recalls Vehicles for Instrument Cluster Software Defect

    Mercedes-Benz is recalling specific 2020-2021 models because instrument cluster software may deactivate interior switch illumination, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, GLE 450, CLA 250, GLS450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V080000·2020-02-13

    RAM Recalls 2019 1500 Trucks for Transfer Case Defect

    Chrysler is recalling 2019 Ram 1500 4WD trucks because a transfer case gear may be installed incorrectly, potentially causing a sudden loss of power or loss of the Park function.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V085000·2020-02-13

    Vermeer Recalls Brush Chipper Trailers Due to Lug Nut Defect

    Vermeer is recalling certain 2016-2020 brush chipper trailers because incorrect lug nuts may loosen, potentially causing the wheel to detach or loss of control.

    Product
    VERMEER — VERMEER AX19, BC1500, BC1000XL, BC1200XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V084000·2020-02-13

    Heartland Recalls 2020 Fifth Wheel Trailers Due to Smoke Detector Placement

    Heartland is recalling 487 fifth wheel trailers because a smoke detector may be incorrectly located in the bedroom, potentially delaying fire warnings.

    Product
    HEARTLAND — HEARTLAND MILESTONE, PIONEER, BIGHORN TRAVELER, ELKRIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V081000·2020-02-13

    Jaguar Recalls 2010 XF Vehicles Due to Fuel Leak Fire Risk

    Jaguar is recalling 2010 XF vehicles with 4.2L engines because a cracked fuel tank outlet flange may leak fuel, increasing fire risk.

    Product
    JAGUAR — JAGUAR XF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V083000·2020-02-13

    BMW Recalls 2019 C 400 X Scooters for Throttle Cable Defect

    BMW is recalling 2019 C 400 X scooters because water in the throttle cable can freeze, causing the throttle to stick and increasing crash risk.

    Product
    BMW — BMW C 400 X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20073·2020-02-13

    Textron Recalls Gas-Powered Off-Road Vehicles Due to Fire Hazard

    Textron Specialized Vehicles is recalling approximately 20,573 gas-powered E-Z-GO, Cushman, and Tracker off-road vehicles because a starter generator wire can contact the exhaust, posing a fire hazard.

    Product
    Gas-powered E-Z-GO, Cushman and Tracker brand off-road vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1002-2020·2020-02-12

    Cardinal Health Recalls AAMI 3 Fabric Reinforced Gowns Due to Contamination

    Cardinal Health is recalling AAMI 3 Fabric Reinforced Gowns due to unknown levels of bioburden, microbiological flora, and particulate contamination.

    Product
    AAMI 3 FABRIC REINFORCEDGown 2XL NS, Item Code 9571NA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1014-2020·2020-02-12

    Cardinal Health Recalls RoyalSilk Gowns Due to Unknown Contamination

    Cardinal Health is recalling RoyalSilk gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.

    Product
    ROYALSILK 3XLARGE/XLONG NS, Gown Item Code 95998N
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V079000·2020-02-12

    2019 Mercedes-Benz and Freightliner Sprinter Vehicles Recalled for Exhaust Leak

    Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vehicles because an exhaust gas leak could increase the risk of a fire.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 1500, SPRINTER 4500, SPRINTER 2500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0927-2020·2020-02-12

    Intuitive Surgical Recalls da Vinci SP Systems Due to Defective Capacitors

    Intuitive Surgical is recalling four da Vinci SP Surgical Systems because defective capacitors on circuit boards may cause vision loss or non-recoverable system errors.

    Product
    da Vinci SP Surgical System, SP1098, 00886874114605 Product Usage: used with an endoscope, surgical instruments, and accessories to perform minimally invasive surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1013-2020·2020-02-12

    Cardinal Health Recalls AAMI 3 Royalsilk Surgical Gowns Due to Contamination

    Cardinal Health is recalling AAMI 3 Royalsilk Surgical Gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.

    Product
    AAMI 3 ROYALSILK SURGGOWN BNS 2XL, Item Code 9578NB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1030-2020·2020-02-12

    Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination

    Cardinal Health is recalling AAMI 3 Nonreinforced Surgical Gowns (4XL) because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.

    Product
    AAMI 3 NONREINF SURGICAL GOWN 4XL, Item Code 9599
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1004-2020·2020-02-12

    Cardinal Health Recalls Surgical Gowns Due to Unknown Contamination

    Cardinal Health is recalling AAMI 3 surgical gowns because they contain unknown levels of bioburden, microbiological flora, and particulate contamination.

    Product
    AAMI 3 FABREINF SURG GOWN L NS, Item Code 9511NB
    Category
    Medical Device
    Distribution
    Distributed nationwide