The Recall Desk

State

American Samoa product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38551–38575 of 73766

  • HighNHTSA·18V314000·2018-05-14

    BMW Recalls 2010-2011 335d Vehicles for Battery Cable Defect

    BMW is recalling 2010-2011 335d vehicles because a battery cable connection may degrade, causing intermittent power loss and unexpected stalling.

    Product
    BMW — BMW 335D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V310000·2018-05-14

    Trail Boss Recalls One Horse Trailer Due to Propane Leak Risk

    Trail Boss is recalling one 2017 Twister Horse Trailer because a loose or missing propane gas valve screw may allow gas to leak, increasing fire risk.

    Product
    TRAIL BOSS — TRAIL BOSS TWISTER HORSE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V309000·2018-05-13

    MCI Motor Coaches Recalled for Exhaust Pipe Fire Risk

    Motor Coach Industries is recalling 1,123 motor coaches because exhaust bellow pipes may develop holes, allowing hot gases to leak and increase fire risk.

    Product
    MCI — MCI D4000, D4500, D4005, D4505
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V308000·2018-05-11

    Kenworth Recalls 2018 T270 Trucks Due to Front Wheel Hub Defect

    PACCAR is recalling 2018 Kenworth T270 trucks because an incorrectly installed front wheel hub component may cause bearing failure and wheel separation.

    Product
    KENWORTH — KENWORTH T270
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V306000·2018-05-11

    Navistar Recalls 2019 International LT Trucks for Brake Drum Defect

    Navistar is recalling 2019 International LT heavy diesel trucks because lightweight brake drums may overheat, crack, or separate, increasing crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V307000·2018-05-11

    Newmar Recalls 2016-2018 Mountain Aire Motorhomes for Tire Damage Risk

    Newmar is recalling 2016-2018 Mountain Aire motorhomes because the DEF tank bracket may contact the tag axle tire, potentially causing tire failure and increasing crash risk.

    Product
    NEWMAR — NEWMAR MOUNTAIN AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V304000·2018-05-10

    GM Recalls 2016-2018 Chevrolet Cruze Vehicles for Fuel Leak Risk

    General Motors is recalling 2016-2018 Chevrolet Cruze LS vehicles because they may leak gasoline after a rear-impact crash and rollover, increasing fire risk.

    Product
    CHEVROLET — CHEVROLET CRUZE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18152·2018-05-10

    ALDI Recalls Ambiano Mini Deep Fryers Due to Fire and Burn Hazards

    ALDI is recalling Ambiano mini deep fryers because the heating element can overheat, posing fire and burn hazards. Three fire incidents and minor property damage have been reported.

    Product
    Ambiano mini deep fryers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18153·2018-05-10

    Munchkin Recalls Waterpede Bath Toys Due to Choking Hazard

    Munchkin is recalling Waterpede bath toys because they can break apart and expose small beads, posing a choking hazard to young children.

    Product
    Waterpede™ children's bath toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18741·2018-05-10

    Tobi Recalls Babynest Crib Bumpers Due to Strangulation Hazard

    Tobi USA LLC is recalling Babynest crib bumpers sold online at babybay.us because the strings pose a strangulation hazard to babies.

    Product
    Babynest crib bumpers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18154·2018-05-10

    illy Recalls 8.8-Ounce Whole Bean Coffee Cans Due to Lid Injury Hazard

    illy is recalling about 65,000 8.8-ounce whole bean coffee cans because the lid can detach suddenly with force upon opening, posing an injury hazard.

    Product
    illy 8.8-ounce whole bean coffee cans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1478-2018·2018-05-09

    FDA Recalls Kratom Powder Due to Potential Salmonella Contamination

    Viable Solutions, LLC is recalling Mitragyna Speciosa Leaf Powder (Kratom) because it may be contaminated with Salmonella.

    Product
    Mitragyna Speciosa Leaf Powder-Thai Maeng Da, sold under the brand name Herbal-Salvation.com. The powder is packaged in kraft paper, foil-lined heat sealed pouches and sold in 25g, 100g, 250g, and 1000g. The product label is read in parts: "***herbal-salvation***Mitragyna…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1477-2018·2018-05-09

    Viable Solutions Recalls Mitragyna Speciosa Leaf Powder Due to Salmonella Risk

    Viable Solutions, LLC is recalling Mitragyna Speciosa Leaf Powder (Green Horn) sold as Herbal-Salvation.com due to potential Salmonella contamination.

    Product
    Mitragyna Speciosa Leaf Powder-GREEN Horn, sold under the brand name Herbal-Salvation.com. The powder is packaged in kraft paper, foil-lined heat sealed pouches and sold in 25g, 100g, 250g, and 1000g. The product label is read in parts: "***herbal-salvation***Mitragyna…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0703-2018·2018-05-09

    AuroMedics Recalls Linezolid Injection Bags Due to Sterility Concerns

    AuroMedics Pharma LLC is recalling Linezolid Injection bags due to a lack of assurance of sterility and a confirmed report of leaking bags with mold.

    Product
    LINEZOLID — LINEZOLID (LINEZOLID)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0705-2018·2018-05-09

    AuroMedics Recalls Levetiracetam Injection Due to Sterility Concerns

    AuroMedics Pharma LLC is recalling 261,250 bags of Levetiracetam Injection due to a confirmed report of leaking bags and mold found between the outer bag and overwrap.

    Product
    LEVETIRACETAM — LEVETIRACETAM (LEVETIRACETAM IN SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0709-2018·2018-05-09

    AuroMedics Recalls Levofloxacin IV Bags Due to Sterility Concerns

    AuroMedics Pharma LLC is recalling 308,112 bags of Levofloxacin in 5% Dextrose Injection due to a lack of assurance of sterility and a confirmed report of mold.

    Product
    LEVOFLOXACIN — LEVOFLOXACIN (LEVOFLOXACIN IN 5% DEXTROSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1603-2018·2018-05-09

    Philips MultiDim Eleva Imaging System Recalled for Uncontrolled Table Rotation

    Philips is recalling 184 MultiDim Eleva imaging systems because a broken actuator fixation can cause the patient table to rotate uncontrollably at high speed.

    Product
    MultiDim Eleva 708032 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1605-2018·2018-05-09

    Philips MultiDiagnost Eleva Imaging System Recalled for Uncontrolled Table Rotation

    Philips is recalling 37 MultiDiagnost Eleva imaging systems because a broken actuator fixation can cause the patient table to rotate uncontrollably at high speed.

    Product
    MultiDiagnost Eleva 708036 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0706-2018·2018-05-09

    AuroMedics Recalls Levetiracetam Injection Due to Sterility Concerns

    AuroMedics Pharma LLC is recalling Levetiracetam Injection due to a lack of assurance of sterility and a confirmed report of leaking bags and mold.

    Product
    LEVETIRACETAM — LEVETIRACETAM (LEVETIRACETAM IN SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1607-2018·2018-05-09

    Philips MD-Eleva Medical Imaging System Recalled for Tilt Actuator Failure

    Philips is recalling 199 MD-Eleva imaging systems because a tilt actuator may break, causing the table to rotate uncontrollably at high speed.

    Product
    Mutlidiagnost-Eleva with Flat Detector Eleva with Flat Detector 708037 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1606-2018·2018-05-09

    Philips MD-Eleva Imaging System Recalled for Uncontrolled Table Rotation

    Philips is recalling 206 MD-Eleva imaging systems because the tilt actuator fixation may break, causing the table to rotate uncontrollably at high speed.

    Product
    Mutlidiagnost-Eleva with Flat Detector 708034 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide