The Recall Desk

State

American Samoa product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30801–30825 of 73747

  • HighCPSC·20040·2019-12-17

    J. Crew Recalls Boys' Denim Pants Due to Choking Hazards

    J. Crew is recalling specific boys' denim pants because small stones from the manufacturing process may remain in the pockets or waistband, posing a choking risk to young children.

    Product
    Crewcuts boys' stone washed denim pants
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V893000·2019-12-16

    Foretravel Recalls 2020 Realm and iH45 Vehicles Due to Brake Defect

    Foretravel is recalling 2020 Realm and iH45 vehicles because a brake relay valve defect may increase stopping distance, raising crash risk.

    Product
    FORETRAVEL — FORETRAVEL REALM, IH-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V896000·2019-12-16

    Mack Trucks Recalls 2020 Models for Steering Drag Link Defect

    Mack Trucks is recalling 2020 Anthem, Granite, and Pinnacle vehicles because steering drag link connections may be improperly installed, risking loss of steering control.

    Product
    MACK — MACK ANTHEM (AN), PINNACLE (CHU), GRANITE (GR)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V894000·2019-12-16

    Maintainer Recalls 2019 Custom Body Heavy Rescue Vehicle for Shock Defect

    Maintainer is recalling one 2019 Custom Body Heavy Rescue vehicle because front shocks may separate, potentially causing a steering fluid leak and loss of power steering assist.

    Product
    MAINTAINER — MAINTAINER CUSTOM BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V892000·2019-12-16

    Mercedes-Benz Recalls CLA Models Due to Air Bag Calibration Issue

    Mercedes-Benz is recalling certain 2015-2018 CLA models because the passenger air bag may not deploy properly in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ CLA 250, CLA250, AMG CLA45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V891000·2019-12-13

    Forest River Recalls 2020 Motorhomes Due to Trailer Hitch Bolt Issue

    Forest River is recalling 2020 Georgetown and FR3 motorhomes because trailer hitch bolts may not be properly tightened, posing a crash risk while towing.

    Product
    FOREST RIVER — FOREST RIVER FR3, GEORGETOWN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-121319·2019-12-13

    USDA Issues Public Health Alert for H-E-B Butter Chicken Soup

    USDA FSIS issued a public health alert for H-E-B Butter Chicken Soup due to undeclared wheat and soy allergens.

    Product
    FSIS Issues Public Health Alert for Chicken Soup due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V885000·2019-12-12

    Chrysler Recalls 2005-2006 Dodge Viper for Airbag Deployment Defect

    Chrysler is recalling 2005-2006 Dodge Viper vehicles because the Occupant Restraint Control module may inadvertently deploy air bags and seat belt pretensioners, increasing injury risk.

    Product
    DODGE — DODGE VIPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V890000·2019-12-12

    Maintainer Recalls 2019 Custom Body Heavy Rescue Vehicle for Brake Defect

    Maintainer is recalling one 2019 Custom Body Heavy Rescue vehicle because a brake relay valve defect may cause extended stopping distances, increasing crash risk.

    Product
    MAINTAINER — MAINTAINER CUSTOM BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V888000·2019-12-12

    GM Recalls 2019-2020 Silverado and Sierra Trucks for Electrical Fire Risk

    General Motors is recalling 2019-2020 Chevrolet Silverado 1500 and GMC Sierra 1500 trucks because excessive glue on the battery cable may cause electrical arcing, stalling, or fire.

    Product
    GMC — GMC, CHEVROLET SIERRA 1500, SILVERADO 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V889000·2019-12-12

    GM Recalls 2019 Trucks and Sedans for Brake Software Error

    General Motors is recalling 2019 Chevrolet Silverado 1500, GMC Sierra 1500, and Cadillac CT6 vehicles because a software error may disable Electronic Stability Control and Antilock Brake Systems without warning.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC SILVERADO 1500, SIERRA 1500, CT6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V886000·2019-12-12

    Chrysler Recalls 2018-2019 Pacifica for Rearview Camera Software Error

    Chrysler is recalling 2018-2019 Pacifica minivans because a software error may keep the rearview camera image on the radio display after shifting out of reverse, potentially distracting the driver.

    Product
    CHRYSLER — CHRYSLER PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0537-2020·2019-12-11

    Sanofi Recalls Regular Strength Zantac 150 mg Due to NDMA Impurity

    Sanofi-Aventis U.S. LLC is recalling Regular Strength Zantac 150 mg because the FDA detected the NDMA impurity in the product.

    Product
    Regular Strength Zantac 150 mg Distributed by: Chattem, Inc., a Sanofi Company P.O. Box 2219, Chattanooga, TN 37409-0219. NDC 05269-220-25.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0562-2020·2019-12-11

    QuVa Pharma Recalls Fentanyl and Ropivacaine Bags Due to Glass Particulates

    QuVa Pharma is recalling specific lots of fentanyl and ropivacaine injection bags due to the presence of glass particulate matter.

    Product
    fentaNYL 400 mcg/200 mL (2 mcg/mL) 0.1% ROPivacaine HCl 200 mg/200 mL (1 mg/mL) in 0.9% Sodium Chloride , 200 mL bag, Preservative Free, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1207-37
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0559-2020·2019-12-11

    QuVa Pharma Recalls Fentanyl and Bupivacaine Infusions Due to Particulate Matter

    QuVa Pharma is recalling specific lots of fentanyl and bupivacaine infusions due to the potential presence of glass particulate matter.

    Product
    fentaNYL 200 mcg/100 mL (2 mcg/mL) BUPivacaine HCl 0.1% 100 mg/100 mL (1 mg/mL) in 0.9% Sodium Chloride 100 mL CADD Preservative Free, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1255-75
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0552-2020·2019-12-11

    QuVa Pharma Recalls Fentanyl and Ropivacaine Bags Due to Particulate Matter

    QuVa Pharma is recalling specific lots of fentanyl and ropivacaine injection bags due to the presence of particulate matter, including potential glass particles.

    Product
    fentaNYL 500 mcg/250 mL (2 mcg/mL) ROPivacaine HCl 0.2% 500 mg/250 mL (2 mg/mL) in 0.9% Sodium Chloride 250 mL Bag Rx, Preservative Free, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1225-37
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V883000·2019-12-11

    BMW Recalls M5 and M8 Models for Transmission Wiring Defect

    BMW is recalling 2019-2020 M5 and 2020 M8 vehicles because a damaged transmission wiring harness can cause an electrical short, leading to loss of propulsion and increased crash risk.

    Product
    BMW — BMW M5, M8, M8 GRAN COUPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V880000·2019-12-11

    Ford Recalls 2017-2019 Super Duty Trucks for Fire Risk

    Ford is recalling 2017-2019 F-Super Duty trucks because seat belt pretensioner sparks could ignite B-pillar materials, potentially causing a vehicle fire.

    Product
    FORD — FORD F-350 SD, F-250 SD, F-550 SD, F-450 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0540-2020·2019-12-11

    Sanofi Recalls Zantac 75 mg Due to NDMA Impurity

    Sanofi-Aventis U.S. LLC is recalling Regular Strength Zantac 75 mg tablets nationwide because NDMA impurity was detected in the product.

    Product
    Regular Strength Zantac 75 mg, Distributed by: Chattem, Inc., a Sanofi Company P.O. Box 2219, Chattanooga, TN 37409-0219. NDC 50269-222-25.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0536-2020·2019-12-11

    Sanofi Recalls Maximum Strength Zantac 150 mg Due to NDMA Impurity

    Sanofi-Aventis U.S. LLC is recalling Maximum Strength Zantac 150 mg tablets nationwide because an NDMA impurity was detected in the product.

    Product
    Maximum Strength Zantac 150 mg Distributed by: Chattem, Inc., a Sanofi Company P.O. Box 2219, Chattanooga, TN 37409-0219. NDC's 41167-0310-1 41167-0310-2 41167-0310-3 41167-0310-4 41167-0310-6 41167-0310-7 41167-0310-8
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0558-2020·2019-12-11

    QuVa Pharma Recalls Fentanyl Syringes Due to Glass Particulate Matter

    QuVa Pharma is recalling fentanyl 50 mcg/mL syringes because of potential glass particulate matter. The recall covers multiple lots distributed nationwide.

    Product
    fentaNYL 2750 mcg/55 mL (50 mcg/mL) 55 mL Syringe, Preservative Free, Rx, QuVA Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 NDC 70092-1100-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0535-2020·2019-12-11

    Sanofi Recalls Zantac 75 mg Tablets Due to NDMA Impurity

    Sanofi-Aventis U.S. LLC is recalling Regular Strength Zantac 75 mg tablets nationwide because NDMA impurity was detected. This action addresses CGMP deviations.

    Product
    Regular Strength Zantac 75 mg, Distributed by: Chattem, Inc., a Sanofi Company P.O. Box 2219, Chattanooga, TN 37409-0219 NDC's 41167-0300-0, 41167-0300-1, 41167-0300-3, 41167-0300-5, 41167-0300-6, 41167-0300-7, 41167-0300-8
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V879000·2019-12-11

    Volkswagen Recalls 2019 Jetta and Golf Models for Wheel Bearing Defect

    Volkswagen is recalling 2019 Jetta GLI, Golf Alltrack, and Golf GTI vehicles because improperly machined front wheel bearings may cause excessive stress, increasing the risk of a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA, GOLF ALLTRACK, GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide