The Recall Desk

State

American Samoa product recalls

73,598 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 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29726–29750 of 73623

  • HighCPSC·20081·2020-02-27

    Step2 Recalls Children's Grocery Shopping Carts Due to Laceration Hazard

    Step2 is recalling about 17,000 Little Helper's children's grocery shopping carts because the baskets can break into sharp pieces, posing a laceration hazard.

    Product
    Little Helper's™ children's grocery shopping carts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0711-2020·2020-02-26

    Hungry Root Dairy Free Garlic Parmesan Sauce Recalled for Undeclared Cashews

    The Honest Stand is recalling Hungry Root Dairy Free Garlic Parmesan Sauce because it contains cashews that were not listed on the physical packaging.

    Product
    Hungry Root Dairy free Garlic Parm sauce, Packaged in 9 oz. polypropylene dip containers with lidding film and lid, packed in 24 count master cases. Distributed by Hungry Root Inc. NY, NY 10003
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1278-2020·2020-02-26

    FDA Recalls Polysorb Sutures Due to Packaging Integrity Issues

    The FDA is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that could compromise sterility.

    Product
    Polysorb Braided Absorbable Suture 1 30 VIOLET GS-22, Item Code CL885 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V112000·2020-02-26

    Nissan Recalls 2020 Versa Vehicles for Fuel Tank Manufacturing Defect

    Nissan is recalling 2020 Versa vehicles because a manufacturing issue may cause a small hole in the fuel tank seam, potentially leading to a fuel leak and fire risk.

    Product
    NISSAN — NISSAN VERSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0850-2020·2020-02-26

    NCS Healthcare Recalls Glycopyrrolate Tablets Due to Impurity Failure

    NCS Healthcare of Kentucky Inc is recalling 6,929 blister cards of Glycopyrrolate Tablets, USP, 1 mg, due to high out-of-specification results for an unknown impurity.

    Product
    Glycopyrrolate Tabs, USP, 1 mg, 30-count unit dose blister card, FOR INSTITUTIONAL USE ONLY, Rx Only, Packaged by Vangard, Glasgow, KY 42141; NDC 0615-8170-39.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0705-2020·2020-02-26

    ABH Nature's Products Recalls All Dietary Supplements for cGMP Violations

    ABH Nature's Products Inc. is recalling all dietary supplements under a consent decree because they were prepared, packed, or held in violation of current good manufacturing practice regulations.

    Product
    All Dietary Supplement manufactured and distributed by ABH Nature's Products Inc.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1333-2020·2020-02-26

    Siemens Uroskop Omnia max Recalled for Collision Control Override Risk

    Siemens is recalling 192 Uroskop Omnia max devices because a bypass key can override collision controls, creating a risk of collision with obstacles or persons.

    Product
    Uroskop Omnia max, Model No. 10762473 - Product Usage: Uroskop Omnia Max is a device intended to visualize anatomical structures by converting an Xray pattern into a visible image. The system is designed primarily for urological diagnosis and the support of urological…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1286-2020·2020-02-26

    Recall of Polysorb Sutures Due to Potential Packaging Integrity Issues

    Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Sutures due to potential packaging integrity issues that could impact sterility.

    Product
    Polysorb Braided Absorbable Suture 2-0 VIOLET 30" V-20, Item Code GL123 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0708-2020·2020-02-26

    Dragonfly Botanicals Breathe Deep Recalled for Internal Use of Coltsfoot

    Green Water, LLC is recalling Dragonfly Botanicals Breathe Deep dietary supplements because they contain Coltsfoot, which is not to be used internally.

    Product
    Dragonfly Botanicals Full spectrum Breathe Deep 1000mg/oz Dietary Supplement, sold in 0.5 oz, 1 oz, 2 oz, and 4 oz amber glass bottles with dropper.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0707-2020·2020-02-26

    Taspen's Organics Breathe Easy Herbal Tincture Recalled for Coltsfoot

    Green Water, LLC is recalling Taspen's Organics Breathe Easy Herbal Tincture because it contains Coltsfoot, which is not to be used internally.

    Product
    Taspen's Organics Breathe Easy Herbal Tincture Dietary Supplement, sold in 1 oz, 2 oz, and 4 oz amber glass bottles with dropper.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1290-2020·2020-02-26

    Polysorb Braided Absorbable Suture Recalled for Packaging Integrity Issues

    Covidien LLC is recalling specific lots of Polysorb Braided Absorbable Suture due to potential packaging integrity issues that may impact the humidity or sterility barrier.

    Product
    Polysorb Braided Absorbable Suture 3/0 30" UNDYED V-20, Item Code GLS322 - Product Usage: Indicated for use in soft tissue approximation or ligation and ophthalmic surgery, but not in cardiovascular or neural tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0724-2020·2020-02-26

    Safeway Chocolate Buttercreme Base Recalled for Plastic Polymer Contamination

    CSM Bakery Products is recalling 45 lb. boxes of Safeway Chocolate Buttercreme Base because pieces of plastic polymer were introduced into the sugar system.

    Product
    45 lb. box SAFEWAY CHOCOLATE BUTTERCREME BASE, MDM # 10201865, Distributed by Safeway Inc. PO Box 99 Pleasanton, CA 94566-0009
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·20078·2020-02-26

    Safavieh Recalls Aura and Silas Chests Due to Tip-Over Hazards

    Safavieh is recalling Aura and Silas 3-drawer chests because they can tip over or entrap children if not anchored to the wall.

    Product
    Aura and Silas 3-Drawer Chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1264-2020·2020-02-26

    Recall of Covidien Endo GIA Ultra Universal Staplers Due to Sterility Risk

    COVIDIEN LLC is recalling 2,180 units of Endo GIA Ultra Universal Staplers because the sterile barrier may be compromised, increasing the risk of infection.

    Product
    Covidien Endo GIA Ultra Universal Stapler 12 mm-intended for resection, transection in general surgery Item Code: EGIAUSTND
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1314-2020·2020-02-26

    Nobel Biocare Dense Bone Drill Recall Due to Sterility Concerns

    Nobel Biocare is recalling Dense Bone Drills because a packaging sealing issue may compromise sterility during shelf life.

    Product
    Dense Bone Drill NP 3.5x16 mm Single-Pat - Product Usage: Drills are intended to be used in the upper and lower jaw bone to prepare osteotomy prior to implant placement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0723-2020·2020-02-26

    CSM Bakery Products Recalls Donut Icing Due to Plastic Polymer Contamination

    CSM Bakery Products is recalling 43 lb. pails of Glossy White Icing distributed by Krispy Kreme because pieces of plastic polymer were introduced into the sugar system.

    Product
    43 lb. pail GLOSSY WHITE ICING (1102507) donut icing, MDM # 10199098, Distributed by Krispy Kreme Doughnut Corporation 1814 Ivy Avenue, Winston-Salem, NC 27105
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1235-2020·2020-02-26

    Cardinal Health Recalls Presource Procedure Packs with Potential Sterility Issues

    Cardinal Health is recalling Presource Procedure Packs containing AAMI Level 3 surgical gowns because they may not be sterile due to improper environmental conditions during manufacturing.

    Product
    Presource Procedure Packs containing AAMI Level 3 surgical gowns, Multiple Catalog Numbers Produced Between September 1, 2018 and January 15, 2020. Additional kits produced through February 19, 2020 were included.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1315-2020·2020-02-26

    Nobel Biocare Dense Bone Drills Recalled for Sterility Concerns

    Nobel Biocare is recalling Dense Bone Drills because a packaging defect may compromise sterility during shelf life.

    Product
    Dense Bone Drill WP 5x13 mm Single-Pat - Product Usage: Drills are intended to be used in the upper and lower jaw bone to prepare osteotomy prior to implant placement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V111000·2020-02-26

    Custom Fire Recalls 2017 Side Mount Pumper for Foam Pump Overheating

    Custom Fire is recalling one 2017 Side Mount Pumper because the foam pump system can overheat and fail, making firefighting foam unavailable.

    Product
    CUSTOM FIRE — CUSTOM FIRE SIDE MOUNT PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1332-2020·2020-02-26

    Siemens Luminos Agile Max X-ray System Recalled for Collision Risk

    Siemens is recalling 475 Luminos Agile Max X-ray systems because a bypass key can override collision controls, creating a risk of collision with obstacles or persons.

    Product
    Luminos Agile Max, Model No. 10762472 - Product Usage: Luminos Agile Max is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image. The system has medical applications ranging from gastrointestinal examinations to cranial…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1319-2020·2020-02-26

    Nobel Biocare Recalls Implant Retrieval Instruments Due to Sterility Concerns

    Nobel Biocare is recalling 423 implant retrieval instruments because a packaging defect may compromise sterility during shelf life.

    Product
    Implant Retrieval Instrument CC NP & Ext Hex WP 22 mm - Product Usage: They can be used to remove implants, if the implant connection has been damaged. It can be used to remove implants with internal conical connection, internal tri-channel connection or external hex connection.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1329-2020·2020-02-26

    Philips CombiDiagnost PCF X-ray System Software Recall

    Philips is recalling 131 CombiDiagnost PCF X-ray systems due to a software error that locks the table and an incorrectly installed thermos switch.

    Product
    CombiDiagnost PCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic, general purpose.
    Category
    Medical Device
    Distribution
    Distributed nationwide