The Recall Desk

State

American Samoa product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50626–50650 of 73852

  • SevereNHTSA·15V838000·2015-12-14

    Charmac Recalls 2015-2016 Horse and Cargo Trailers Due to Axle Weld Failure

    Charmac is recalling 2015-2016 Horse and Cargo trailers because a weld on the torsion axle may fail, causing the wheel assembly to separate and increasing crash risk.

    Product
    CHARMAC — CHARMAC HORSE TRAILER, CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V837000·2015-12-14

    MCI Recalls 2015 Motor Coaches Due to Missing Axle Welds

    Motor Coach Industries is recalling specific 2015 D4500 and D4505 motor coaches because drive axles may be missing welds on hanger brackets, which could separate and affect vehicle control.

    Product
    MCI — MCI D4500, D4505
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V839000·2015-12-14

    Altec Recalls Manitex/PM Knuckle Boom Cranes Due to Outrigger Weld Cracks

    Altec is recalling 2013-2014 Manitex/PM Knuckle Boom Cranes because outrigger welds may crack, causing failure and increasing the risk of the truck tipping over.

    Product
    MANITEX/PM — MANITEX/PM KNUCKLE BOOM CRANES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V836000·2015-12-11

    McLaren Recalls 2014-2015 P1 Vehicles Due to Hood Latch Defect

    McLaren is recalling 122 model year 2014-2015 P1 hybrid vehicles because the secondary hood latch may fail to re-engage, potentially allowing the hood to open while driving.

    Product
    MCLAREN — MCLAREN P1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V833000·2015-12-11

    GM Recalls 2016 Acadia, Traverse, Enclave for Seat Frame Weld Defect

    General Motors is recalling 2,633 model year 2016 Chevrolet Traverse, GMC Acadia, and Buick Enclave vehicles because the third-row left lower seat frame may have welds in incorrect locations.

    Product
    GMC — GMC, CHEVROLET, BUICK ACADIA, TRAVERSE, ENCLAVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V834000·2015-12-11

    Highland Ridge RV Recalls Fifth Wheels and Travel Trailers for Missing Label

    Highland Ridge RV is recalling specific 2015-2016 fifth wheels and travel trailers because they may be missing a caution label regarding the sewer drain valve.

    Product
    HIGHLAND RIDGE FW — HIGHLAND RIDGE FW, OPEN RANGE OPEN RANGE, 3X, HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V835000·2015-12-11

    Trail Boss Recalls 2013 Bloomer Horse Trailer Water Heater

    Trail Boss is recalling one 2013 Bloomer Horse Trailer because a water heater valve may cause overheating, posing a scalding risk.

    Product
    BLOOMER — BLOOMER HORSE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V832000·2015-12-10

    Roush Recalls 2015 Ford Mustang GT Stage 3 for Brake Caliper Defect

    Roush is recalling 2015 Ford Mustang GT Roush Stage 3 vehicles because a brake caliper guide pin may loosen, reducing rear braking ability and increasing crash risk.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16713·2015-12-10

    Polaris Recalls RZR XP Turbo Vehicles Due to Oil Leak Fire Hazard

    Polaris is recalling about 2,230 RZR XP Turbo recreational off-highway vehicles because an oil drain line leak can cause a fire.

    Product
    Recreational Off-Highway Vehicles (ROV)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V830000·2015-12-10

    GM Recalls 2016 Silverado and Sierra Trucks for Air Bag Sensor Defect

    General Motors is recalling 2016 Chevrolet Silverado and GMC Sierra trucks because a misplaced mounting stud may cause the air bag sensor housing to fracture, potentially preventing air bag deployment in a crash.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO, SIERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15T022000·2015-12-10

    Cooper Zeon LTZ Tires Recalled for Tread Cracking and Lug Chunking

    Cooper Tire & Rubber Co. is recalling specific Zeon LTZ tires manufactured in September 2015 because tread cracking or chunking may cause loss of tire pressure, increasing crash risk.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0392-2016·2015-12-09

    Geritrex Recalls Unapproved Hydrocortisone Suppositories Nationwide

    Geritrex Corp is recalling GRx HiCort 25 suppositories because the FDA determined they are unapproved new drugs and misbranded.

    Product
    GRx HiCort 25 (hydrocortisone acetate 25 mg) Suppositories, 12-count box, Rx only, Distributed by Geritrex Corporation Mount Vernon, NY 10550, NDC 54162-015-12
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0400-2016·2015-12-09

    Western Drug Recalls Butor/Nal/Hydro Nasal Suspension Due to Sterility Concerns

    Western Drug is recalling two containers of Butor/Nal/Hydro Nasal Suspension because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.

    Product
    Butor/Nal/Hydro Nasal Susp, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0461-2016·2015-12-09

    Western Drug Recalls Toradol Injection Due to Sterility Concerns

    Western Drug is recalling Toradol 60mg/mL Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.

    Product
    Toradol 60mg/mL Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0432-2016·2015-12-09

    Western Drug Recalls Jessners Dermal Solution Due to Sterility Concerns

    Western Drug is recalling all lots of Jessners Dermal Solution because the product lacks assurance of sterility. The recall covers distribution in eight US states.

    Product
    Jessners Dermal Solution, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0402-2016·2015-12-09

    Western Drug Recalls Dep-Estradiol Injection Due to Sterility Concerns

    Western Drug is recalling Dep-Estradiol 10 mg/mL Injection because the company cannot ensure the product is sterile. The recall covers 9 containers distributed nationwide.

    Product
    Dep-Estradiol 10 mg/mL Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0453-2016·2015-12-09

    Western Drug Recalls Squaric Acid 4% Injection Due to Sterility Concerns

    Western Drug is recalling Squaric Acid 4% Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.

    Product
    Squaric Acid 4% Inj, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0483-2016·2015-12-09

    Western Drug Recalls Quad Mix Strong Injections Due to Sterility Concerns

    Western Drug is recalling all lots of Quad Mix Strong Injections because the company cannot ensure the product is sterile. The recall covers distribution in eight US states.

    Product
    Quad Mix Strong Inj, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0405-2016·2015-12-09

    Western Drug Recalls Furosemide Solution Due to Sterility Concerns

    Western Drug is recalling Furosemide 20 mg/mL solution because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.

    Product
    Furosemide 20 mg/mL svn Sol, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0471-2016·2015-12-09

    Western Drug Recalls Hydroxocobalamin Injections Due to Sterility Concerns

    Western Drug is recalling Hydroxocobalamin 1mg Injections because the company cannot guarantee the product is sterile.

    Product
    Hydroxocobalamin 1mg Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide