The Recall Desk

State

American Samoa product recalls

73,376 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 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20001–20025 of 73401

  • HighFDA (Food)·F-1345-2022·2022-06-29

    Ice cream recall for undeclared tree nut allergen

    Red Button Vintage Creamery Canadian Vanilla Ice Cream was distributed nationwide with undeclared almond allergen due to packaging mix-up. Consumers with tree nut allergies should not consume this product.

    Product
    Red Button Vintage Creamery Canadian Vanilla Ice Cream, 56 ounce tub, UPC 0 77865 01001 7, Distributed by Associated Foods Stores, Salt Lake City, UT, 84119. Store Frozen.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1273-2022·2022-06-29

    FDA Recalls Catheter Drainage Kits With Wrong Needle Size

    Bard Peripheral Vascular Inc is recalling certain catheter drainage kits that may contain an 8 Fr needle instead of the correct 6 Fr needle. The incorrect needle size could cause tissue injury during patient care.

    Product
    REF: PIG1260K, 6Fr, X10, Safe-t-Centesis Catheter drainage Kit, Sterile EO,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1347-2022·2022-06-29

    Kava Glycerite Recalled Due to High Yeast and Mold Contamination

    EarthLab Inc is recalling Wise Woman Herbals Standardized Kava Glycerite due to high yeast and mold counts detected during microbial testing. The affected product was distributed nationwide.

    Product
    Wise Woman Herbals Standardized Kava Glycerite, product is liquid and contains 15 mg Kavalactones (from Piper methysticum) and 9 mg Kavalactones (from Piper methysticum) depending on lot. Dosage: 60 drops 1-2 times a day. Product is packaged in Amber Glass Boston Round…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1151-2022·2022-06-29

    Isopropyl Alcohol bottles recalled for defective containers and leakage

    Vi-Jon's 70% isopropyl alcohol bottles may leak when squeezed or tilted due to defects in the bottle neck finish. Over 3 million bottles with various lot numbers were distributed nationwide.

    Product
    ISOPROPYL ALCOHOL — ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1155-2022·2022-06-29

    Clonazepam Tablets Recalled Due to Manufacturing Defect

    Sun Pharmaceutical is recalling Clonazepam Orally Disintegrating Tablets (0.125mg) due to manufacturing defects where oversized tablets were found. The affected lot (MHC1430A, exp. 09/2023) was distributed nationwide.

    Product
    Clonazepam Orally Disintegrating Tablets, USP, 0.125mg, Rx Only, 60 Tablets, Mfd. by: Sun Pharmaceutical Industries Ltd. Mumbai, India, Dist. by: Sun Pharmaceutical Industries In., Cranbury, NJ 08512, NDC 57664-783-68, packaged in bottles.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1281-2022·2022-06-29

    BVI Wet-Field Eraser surgical devices shipped with incorrect tip configuration

    Beaver Visitec International recalled 660 units of BVI Wet-Field Eraser surgical devices after discovering boxes labeled with one tip configuration contained a different tip design. This mismatch could affect surgical precision and hemostasis control.

    Product
    BVI Wet -Field Eraser, 18GA Blunt Tip, 45Deg.-Intended to remove tissue and control bleeding by the use of high frequency electrical current Part Number: 221251
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1282-2022·2022-06-29

    INTERGARD Woven Vascular Graft mislabeled with incorrect size specification

    Maquet Cardiovascular recalls INTERGARD Woven Vascular Grafts with incorrect labeling. Units labeled as 8 mm diameter instead contained 32 mm diameter grafts.

    Product
    INTERGARD Woven Vascular Graft is a woven polyester graft coated with a bovine collagen. It has an external velour surface and non-velour inner surface. The device is available in straight tubes and bifurcated configurations, as well as hemabridge, aortic arch, thoracic aortic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1283-2022·2022-06-29

    Cardiac device software recalled for inadequate electrical insulation

    CardioTek EP-TRACER Software V2.x is recalled because it failed electrical safety testing for insulation. The 146 affected units were distributed worldwide.

    Product
    CardioTek EP-TRACER Software V2.x.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1275-2022·2022-06-29

    EVIS EXERA II Gastrointestinal Videoscope Recalled for Incorrect Component Fit

    Olympus is recalling 8 EVIS EXERA II gastrointestinal videoscopes (Model GIF-HQ190) because an incorrect rubber component may have been installed during repair. The incorrect part does not meet the device's design specifications.

    Product
    EVIS EXERA II Gastrointestinal Videoscope-indicated for use within the upper digestive tract (including the esophagus, stomach, and duodenum). Model: GIF-HQ190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1346-2022·2022-06-29

    Wise Woman Herbals Kava Capsules recalled for yeast and mold contamination

    EarthLab Inc is recalling Wise Woman Herbals Kava Capsules nationwide due to microbial contamination. Quality testing found yeast and mold counts that exceeded acceptable levels.

    Product
    Wise Woman Herbals Kava Capsules, 450 mg Kava (Piper met. Root), Dosage: 1 capsule up to 3 times per day day at 450mg Kava root. 90 counts per bottle. UPC 7 48840 14284 8. Kava Capsules older lots are packaged in 250cc Wide Mouth Amber Glass Packer, Black 45/400 PP ribbed…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1348-2022·2022-06-29

    Wise Woman Herbals Sleepytime Glycerite Recalled for Yeast and Mold Contamination

    EarthLab Inc is recalling Wise Woman Herbals Sleepytime Glycerite due to elevated yeast and mold levels detected in microbial testing. Consumers should discontinue use.

    Product
    Wise Woman Herbals Sleepytime Glycerite. Product is liquid and strength is 20% presence in formula. Dosage: 60 drops 1-4 times a day. Product is packaged in Amber Glass Boston Round bottle, Black serrated polypropylene dropper assembly with rubber bulb (2oz only) or Black…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1152-2022·2022-06-29

    FDA Recalls Clonidine Transdermal Patches for Delivery System Defect

    Mayne Pharma is recalling 1,440 cartons of Clonidine transdermal patches nationwide due to an out-of-specification defect in the release liner that could affect proper drug delivery.

    Product
    CLONIDINE — CLONIDINE (CLONIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·020-2022·2022-06-28

    Creminelli Recalls Mini Parmesan Salami Sticks Due to Undeclared Egg Allergen

    Creminelli Fine Meats is recalling approximately 4,207 pounds of mini parmesan salami sticks because the product contains an undeclared egg allergen.

    Product
    Creminelli Operating LLC — Creminelli Fine Meats Recalls Mini Parmesan Salami Stick Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V459000·2022-06-28

    Hyundai Recalls 2017-2018 Ioniq Hybrids for Fire Risk

    Hyundai is recalling 2017-2018 Ioniq Hybrid and Plug-in Hybrid vehicles because a power relay assembly may overheat, increasing the risk of a fire.

    Product
    HYUNDAI — HYUNDAI IONIQ HYBRID, IONIQ PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V458000·2022-06-27

    2020-2022 Hyundai Venue seat belt pretensioners may explode in crash

    Hyundai is recalling 2020-2022 Venue vehicles because the front seat belt pretensioners may explode when deployed in a crash, potentially projecting metal fragments at occupants.

    Product
    HYUNDAI — HYUNDAI VENUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V452000·2022-06-24

    Airstream Recalls 2022 Travel Trailers Due to Hub Assembly Defect

    Airstream is recalling 2022 Caravel, Flying Cloud, Globetrotter, International, and Pottery Barn travel trailers because a bearing washer may crack, causing the hub to separate from the axle.

    Product
    AIRSTREAM — AIRSTREAM POTTERY BARN, CARAVEL, INTERNATIONAL, GLOBETROTTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V455000·2022-06-24

    2022 Lincoln Navigator Headlight Control Software Defect Causes Light Failure

    Ford is recalling certain 2022 Lincoln Navigator vehicles due to headlight control module software that may fail, causing side marker and daytime running lights to go dark. This increases crash risk from reduced visibility.

    Product
    LINCOLN — LINCOLN NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V451000·2022-06-24

    2022 Ford Bronco Windshield May Separate During Crash

    Certain 2022 Ford Broncos and Rangers have windshields that may not be properly bonded and could separate during a crash, increasing injury risk.

    Product
    FORD — FORD RANGER, BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V457000·2022-06-24

    2021 Nissan Frontier transmission parking pawl failure may cause vehicle rollaway

    Certain 2020-2022 Nissan Frontier and Titan vehicles have a defective transmission parking pawl that may not engage when shifted to park, creating a rollaway risk. Dealers will replace the component at no cost.

    Product
    NISSAN — NISSAN TITAN, FRONTIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V454000·2022-06-24

    2022 Lincoln Aviator Engine Rails Defect Increases Crash Injury Risk

    Ford is recalling certain 2022 Lincoln Aviator vehicles due to improperly heat-treated engine rails that may reduce structural protection in crashes and potentially detach while driving. Owners should contact Ford for a free inspection and replacement.

    Product
    FORD — FORD, LINCOLN EXPLORER, AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V450000·2022-06-24

    2022 Forest River R-POD Trailers Recalled for Incorrect Axle Rating

    Forest River is recalling 205 2022 R-POD travel trailers because the Federal Placard shows an incorrect axle rating (4400 lbs instead of 3500 lbs), which can cause overload and loss of control.

    Product
    FOREST RIVER — FOREST RIVER R-POD
    Category
    Vehicle
    Distribution
    Distributed nationwide