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.

47801–47825 of 73852

  • HighCPSC·16228·2016-07-19

    Things Remembered Recalls Children's Jewelry Due to Lead Violation

    Things Remembered is recalling silver bracelets and charm necklaces for children because the clear surface coating contains lead in excess of allowable limits.

    Product
    Silver bracelets and charm necklaces
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·056-2016 EXP·2016-07-15

    ConAgra Recalls Frozen Chicken and Beef Entrées Due to Metal Contamination

    ConAgra Foods is recalling approximately 195,597 pounds of frozen P.F. Chang's Home Menu chicken and beef products due to potential metal contamination. No injuries have been reported.

    Product
    Conagra Brands (Conagra Foods Packaged Foods, LLC) — ConAgra Foods Recalls Frozen Chicken and Beef Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·16757·2016-07-15

    Nestlé AccuPure Water Dispensers Recalled for Fire and Burn Hazards

    Nestlé Waters North America is recalling AccuPure countertop water dispensers because they can overheat, melt, and smoke, posing fire and burn risks.

    Product
    AccuPure countertop filtered water dispensers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·16223·2016-07-14

    Flushmate III Pressure-Assist Flushing Systems Recalled for Bursting Hazard

    Flushmate is recalling about 453,000 Flushmate III Pressure-Assist Flushing Systems in the U.S. because the units can burst, posing impact and laceration hazards.

    Product
    Flushmate® III Pressure-Assist Flushing Systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16224·2016-07-14

    Home Source Recalls Floor Lamps Due to Fire and Shock Hazards

    Home Source is recalling about 2,700 floor lamps sold in the New York area and online because defective sockets can cause fires and electric shocks.

    Product
    Floor lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V536000·2016-07-14

    Altec Recalls 2015-2016 Aerial Devices and Digger Derricks for Winch Defect

    Altec is recalling 252 model year 2015-2016 Aerial Devices and Digger Derricks because a hydraulic motor shaft may fail, causing unexpected winch movement and increasing injury risk.

    Product
    ALTEC — ALTEC DIGGER DERRICK, AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16226·2016-07-14

    IKEA Recalls Safety Gates and Extensions Due to Fall Hazard

    IKEA is recalling PATRULL safety gates and extensions because the locking mechanism can open unexpectedly, posing a fall hazard to children.

    Product
    Safety gates and safety gate extensions
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16225·2016-07-14

    Liquid Plumr Clog Removers Recalled for Non-Child-Resistant Caps

    The Clorox Company is recalling three Liquid Plumr clog remover products because the bottles lack required child-resistant closures, posing a risk of chemical burns.

    Product
    Liquid Plumr® Pro-Strength Foaming Clog Fighter®, Liquid Plumr® Industrial Strength Urgent Clear® and Liquid Plumr® Pro-Strength Urgent Clear® clog removers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1149-2016·2016-07-13

    XCEL Capsules Recalled for Undeclared Fluoxetine and Phenolphthalein

    Bee Extremely Amazed LLC is recalling XCEL Capsules marketed as a dietary supplement because they contain undeclared fluoxetine and phenolphthalein.

    Product
    XCEL Capsules, 300 mg, 60-count bottles, Manufactured for JNS Health
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1145-2016·2016-07-13

    Prime Capsules Recalled for Undeclared Sibutramine and Phenolphthalein

    Bee Extremely Amazed LLC is recalling Prime Capsules because they contain undeclared sibutramine and phenolphthalein, making them unapproved drugs.

    Product
    Prime Capsules, 500mg, 60-count bottles, Distributed By Zagonfly 3129 25th St. #392 Columbus, IN 47203
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1144-2016·2016-07-13

    Oasis Capsules Recalled for Undeclared Sibutramine and Phenolphthalein

    Bee Extremely Amazed LLC is recalling Oasis Capsules because they contain undeclared sibutramine and phenolphthalein, making them unapproved drugs.

    Product
    Oasis Capsules, 500mg, 45-count bottles, Manufactured for: MWN Health 37 N Orange Ave Suite 500 Orlando FL 32801 (407)930-4043
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1151-2016·2016-07-13

    ZI XIU TANG Beauty Capsules Recalled for Undeclared Sibutramine

    Bee Extremely Amazed LLC is recalling ZI XIU TANG Beauty Face & Figure Capsules because they contain undeclared sibutramine, a withdrawn drug.

    Product
    ZI XIU TANG BEAUTY FACE & FIGURE Capsules, 250 mg, 60-count bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1143-2016·2016-07-13

    La' Trim Plus Capsules Recalled for Undeclared Withdrawn Ingredients

    Bee Extremely Amazed LLC is recalling La' Trim Plus Capsules because the product contains undeclared sibutramine and phenolphthalein, both withdrawn from the US market for safety reasons.

    Product
    La' Trim Plus Capsules, 350 mg, 60-count bottles, Manufactured for: MWN Health 37 N Orange Ave Suite 500 Orlando, FL 32801 (407) 930-4043
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1654-2016·2016-07-13

    Harris Teeter Soup Mix Recalled for Listeria Risk

    The Pictsweet Company is recalling Harris Teeter brand Soup Mix Veggies due to the possibility of Listeria monocytogenes contamination in the onions.

    Product
    Harris Teeter(TM) brand SOUP MIX VEGGIES, carrots, potatoes, corn, green beans, lima beans, okra, green peas, celery, onions, NET WT 12 OZ (340g), UPC 72036 71683, PROUDLY DISTRIBUTED BY HARRIS TEETER, LLC, MATTHEWS, NC 28105
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1137-2016·2016-07-13

    Hospira Recalls Magnesium Sulfate Injection Due to Particulate Matter

    Hospira Inc. is recalling specific lots of Magnesium Sulfate Injection due to confirmed particulate matter. The recall covers 88,500 vials distributed in the US and several Middle Eastern countries.

    Product
    Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq Magnesium/mL, 20 mL Single-dose vial, packaged in 25 vials per box, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2168-02, barcode (01) 2 030409 216802 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1141-2016·2016-07-13

    Bee Extremely Amazed LLC Recalls Infinity Capsules Tainted With Sibutramine

    Bee Extremely Amazed LLC is recalling Infinity Capsules because the product was found to contain undeclared sibutramine, a withdrawn appetite suppressant.

    Product
    Infinity Capsules, 500 mg, 30-count bottle, Manufactured for Floyd Nutrition
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1661-2016·2016-07-13

    Pictsweet Vegetables for Cajun Gumbo Recalled for Listeria Risk

    The Pictsweet Company is recalling Vegetables for Cajun Gumbo because the onions used in the product may be contaminated with Listeria monocytogenes.

    Product
    PICTSWEET(R) Vegetables for Cajun Gumbo, Seasoned with a blend of Cajun Spices, NET WT 12 OZ (340g), UPC 70560 95818, DISTRIBUTED BY THE PICTSWEET COMPANY, BELLS, TN 38006
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1657-2016·2016-07-13

    Kroger Vegetable Stir Fry Starters Recalled for Listeria Risk

    The Pictsweet Company is recalling Kroger Vegetable Stir Fry Starters because the onions used in the product may be contaminated with Listeria monocytogenes.

    Product
    Kroger(R) VEGETABLES WITH NOODLES, egg noodles, broccoli, carrots, green bell peppers, mushrooms, onions & red bell peppers, STIR FRY STARTERS(R), NET WT 12 OZ (340g), UPC 11110 89776, DISTRIBUTED BY THE KROGER COMPANY, CINCINNATI, OH 45202
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1148-2016·2016-07-13

    FDA Recalls Ultimate Formula Capsules Tainted With Undeclared Sibutramine

    Bee Extremely Amazed LLC is recalling Ultimate Formula Capsules because they contain undeclared sibutramine, a withdrawn drug.

    Product
    Ultimate Formula Capsules, 250mg, 48-count bottles, Manufactured for: Zi Xiu Tang Success, LLC Trexlertown, PA 18087, USA www.zixiutangsuccess.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1154-2016·2016-07-13

    Cantrell Drug Recalls Subpotent Fentanyl Citrate Injection Syringes

    Cantrell Drug Company is recalling 42 syringes of fentanyl citrate injection because the drug was subpotent. The recall is voluntary and nationwide.

    Product
    fentaNYL Citrate 1 MCG/mL in 0.9% Sodium Chloride Injection, in 3 mL Syringe, Rx Only, Cantrell Drug Co., Little Rock, AR --- UPC: 9999992131
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1147-2016·2016-07-13

    SLIM TRIM U Capsules Recalled for Undeclared Sibutramine

    Bee Extremely Amazed LLC is recalling SLIM TRIM U Capsules because they contain undeclared sibutramine, a withdrawn drug.

    Product
    SLIM TRIM U Capsules, 250mg, 60-count bottles, Manufactured for Floyd Nutrition
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1157-2016·2016-07-13

    Cantrell Drug Recalls Subpotent Fentanyl Citrate Injection Syringes

    Cantrell Drug Company is recalling 148 syringes of fentanyl citrate injection because the drug was subpotent. The recall is voluntary and nationwide.

    Product
    fentaNYL CITRATE 4 MCG/mL in 0.9% SODIUM CHLORIDE Injection, in 1 mL Syringe, Rx Only, Cantrell Drug Co., Little Rock, AR --- UPC: 9999993491
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1165-2016·2016-07-13

    FDA Recalls Zero Xtreme Fat Burner for Unapproved Ingredients

    The FDA is recalling Zero Xtreme High Performance Fat Burner capsules because testing found unapproved ingredients. Consumers should stop using the product.

    Product
    Zero Xtreme High Performance Fat Burner capsules, 30-count bottle, Distributed by Xtreme Z Distributors, Inc., Miami, FL 33180
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1138-2016·2016-07-13

    Asset BOLD Capsules Recalled for Undeclared Sibutramine and Phenolphthalein

    Bee Extremely Amazed LLC is recalling Asset BOLD Capsules because they contain undeclared sibutramine and phenolphthalein, making them unapproved drugs.

    Product
    Asset BOLD Capsules, 500 mg, 60-count bottles, Distributed by Descor, LLC www.assetcapsules4u.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1142-2016·2016-07-13

    Jenesis Capsules Recalled for Undeclared Sibutramine and Phenolphthalein

    Bee Extremely Amazed LLC is recalling Jenesis Capsules marketed as a dietary supplement because they contain undeclared sibutramine and phenolphthalein, both withdrawn from the US market for safety reasons.

    Product
    Jenesis Capsules, 350 mg, 60-count bottles, Manufactured for Timeless Solutions 1810 E. Sahara Ave #100 Las Vegas, Nevada 89104
    Category
    Drug
    Distribution
    Distributed nationwide