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.

38651–38675 of 73766

  • HighFDA (Drugs)·D-0721-2018·2018-05-02

    FDA Recalls LIPO-DEN Injectable Due to Unknown Particulate Matter

    Coastal Meds, LLC. is recalling 1,309 vials of LIPO-DEN Injectable-30 mL because of the presence of unknown particulate matter.

    Product
    LIPO-DEN Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·18V274000·2018-05-02

    Winnebago Recalls 2018-2019 RVs Due to Roof Rack Fastener Defect

    Winnebago is recalling 293 recreational vehicles because roof racks may detach due to incorrect fasteners, creating a road hazard.

    Product
    WINNEBAGO — WINNEBAGO ERA, REVEL, TRAVATO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1500-2018·2018-05-02

    Stryker T4 Pullover Toga Recalled for Potential Material Separation

    Stryker is recalling T4 Pullover Toga sterile garments because material layers may separate, posing a risk of exposure to contaminants.

    Product
    T4 Pullover Toga, (S/M); Catalog Number: 0400-710-000 Sterile personal protection garment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1510-2018·2018-05-02

    Stryker T5 Zipper Toga Sterile Garment Recall for Layer Separation

    Stryker is recalling T5 Zipper Toga sterile garments because material layers may separate, posing a risk of exposure to contaminants.

    Product
    T5 Zipper Toga with Peel-Away Face Shield, (XL/T); Catalog number: 0400-850-100 Sterile personal protection garment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1476-2018·2018-05-02

    Zimmer Biomet Recalls ZMS Intramedullary Fixation Smooth Guide Wires

    Zimmer Biomet is recalling ZMS Intramedullary Fixation Smooth Guide Wires due to potential failure of the sterile packaging seal.

    Product
    ZMS Intramedullary Fixation Smooth Guide Wire Bullet Tip 3.0 mm Diameter, 100 cm Length; Item Number: 47-2237-038-00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1468-2018·2018-05-02

    Zimmer Biomet Recalls Natural Nail System Tear Drop Guide Wires

    Zimmer Biomet is recalling 19,483 Natural Nail System Tear Drop Guide Wires due to a potential failure of the sterile packaging seal.

    Product
    Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter, 70 cm length; Item Number: 47-2490-098-01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1528-2018·2018-05-02

    EEA Hemorrhoid Stapler Recalled for Potential Welding Defect

    FDA is recalling EEA Hemorrhoid and Prolapse Stapler Sets due to a potential welding defect that could cause bleeding or anastomotic leak.

    Product
    EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 4.8MM, Product Number HEM3348, GTIN Number 1 - 10884521047563, GTIN Number 2 - 20884521047560 Product Usage: The EEA Hemorrhoid and prolapse stapler set with DST Series Technology (instrument) is designed…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1465-2018·2018-05-02

    Zimmer Biomet Recalls Humeral Guide Wires Due to Packaging Seal Failure

    Zimmer Biomet is recalling 19,483 M/DN Intramedullary Fixation Humeral Guide Wires because the sterile packaging seal may fail, potentially compromising sterility.

    Product
    M/DN Intramedullary Fixation Humeral Guide Wire - Smooth 2.4 mm Diameter 70 cm Length Single Use Only; Item Number: 00-2255-025-00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18E029000·2018-05-02

    FiTech Fuel Injection Systems Recalled for Fuel Leak Fire Risk

    Fuel Injection Technology is recalling Summit Racing Max 500-EFI systems because fuel injector O-rings may leak, increasing fire risk.

    Product
    FUEL SYSTEM, GASOLINE:FUEL INJECTION SYSTEM recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1513-2018·2018-05-02

    BioFire FilmArray BCID Panel Recalled for False Positive Proteus Results

    BioFire Diagnostics is recalling the FilmArray BCID Panel because it may produce false positive Proteus results when used with specific BD BACTEC blood culture bottles.

    Product
    FilmArray BCID Panel (Blood Culture Identification Panel), Catalog numbers RFIT-ASY-0126 (30 test kit) and RFIT-ASY-0127 (6 test kit), when used with all lots of BD BACTEC Blood Culture Bottles, Catalog numbers 442020, 442021, 442023, 442192, 442265, 442194, 442022, 442193…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1514-2018·2018-05-02

    Synthes Stem Extractor Recalled Due to Potential Screw Breakage

    Synthes, Inc. is recalling 31 Stem Extractor f/Guide Bar units because the connection screw may break during use.

    Product
    Stem Extractor f/Guide Bar, Part number 03.401.072. Instrumentation for extraction and revision of Epoca shoulder implants.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1131-2018·2018-05-02

    Frozen Parotta Recalled for Undeclared Milk Allergen

    Maharaja Food Importers is recalling frozen Parotta products because the label lists ghee but fails to declare milk, a major allergen.

    Product
    Parotta Family Pack, UPC: 8 70400 00084 5, Frozen; and Small Parotta, UPC: 870400000012, Frozen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1509-2018·2018-05-02

    Stryker T4 Zipper Toga Recall Due to Material Separation Risk

    Stryker is recalling T4 Zipper Toga sterile garments because material layers may separate, creating a risk of exposure to contaminants.

    Product
    T4 Zipper Toga, X-Large; Catalog number: 0400-850-000 Sterile personal protection garment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1527-2018·2018-05-02

    Recall of EEA Hemorrhoid and Prolapse Stapler Sets Due to Welding Defect

    Covidien LLC is recalling EEA Hemorrhoid and Prolapse Stapler Sets because a defective staple guide may cause bleeding or anastomotic leak during surgery.

    Product
    EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM, Product Number HEM3335, GTIN Number 1 - 10884521047518, GTIN Number 2 - 20884521047515 Product Usage: The EEA Hemorrhoid and prolapse stapler set with DST Series Technology (instrument) is designed…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1506-2018·2018-05-02

    Stryker T4 Zipper Toga Sterile Garment Recall for Layer Separation

    Stryker is recalling T4 Zipper Toga sterile personal protection garments because material layers may separate, creating a risk of exposure to contaminants.

    Product
    T4 Zipper Toga, (L/XL); Catalog Number: 0400-820-000 Sterile personal protection garment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0717-2018·2018-05-02

    Coastal Meds Recalls Cyanocobalamin Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling 745 vials of Cyanocobalamin Injectable due to the presence of unknown particulate matter.

    Product
    CYANOCOBALAMIN Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1132-2018·2018-05-02

    MMRF Ela Ada Jaggery Recalled for Undeclared Milk Allergen

    Maharaja Food Importers is recalling frozen MMRF Ela Ada Jaggery because the label lists ghee but fails to declare milk, a major allergen.

    Product
    MMRF Ela Ada Jaggery, UPC: 870400000067, Frozen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1508-2018·2018-05-02

    Stryker T4 Zipper Toga Sterile Garments Recalled for Layer Separation

    Stryker is recalling T4 Zipper Toga sterile personal protection garments because material layers may separate, posing a risk of exposure to contaminants.

    Product
    T4 Zipper Toga, Regular; Catalog number: 0400-830-000 Sterile personal protection garment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1470-2018·2018-05-02

    Zimmer Biomet Recalls ZMS Intramedullary Fixation Smooth Guide Wires

    Zimmer Biomet is recalling ZMS Intramedullary Fixation Smooth Guide Wires due to potential failure of the sterile packaging seal.

    Product
    ZMS Intramedullary Fixation Smooth Guide Wire 3.0 mm Diameter, 100 cm Length; Item Number: 47-2237-037-00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1501-2018·2018-05-02

    Stryker T4 Pullover Toga Recalled for Potential Material Separation

    Stryker is recalling T4 Pullover Toga sterile garments because material layers may separate, posing a risk of exposure to contaminants.

    Product
    T4 Pullover Toga, L/XL; Catalog Number: 0400-720-000 Sterile personal protection garment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·18148·2018-05-02

    Carter's Recalls Children's Cardigan Sets Due to Choking Hazard

    Carter's is recalling 3-piece penguin cardigan sets because the toggle button can detach, posing a choking hazard to young children.

    Product
    3-piece penguin cardigan sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1504-2018·2018-05-02

    Stryker Recalls T4 Pullover Toga Due to Material Separation Risk

    Stryker is recalling T4 Pullover Toga sterile garments because material layers may separate, creating a potential risk of exposure to contaminants.

    Product
    T4 Pullover Toga, X-Large; Catalog Number: 0400-770-000 Sterile personal protection garment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0720-2018·2018-05-02

    Coastal Meds Recalls LIPO-B Injectable Due to Particulate Matter

    Coastal Meds, LLC. is recalling LIPO-B Injectable-30 mL vials due to the presence of unknown particulate matter.

    Product
    LIPO-B Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1502-2018·2018-05-02

    Stryker T4 Pullover Toga Recall Due to Layer Separation Risk

    Stryker is recalling T4 Pullover Toga sterile garments because material layers may separate, posing a risk of exposure to contaminants.

    Product
    T4 Pullover Toga, Regular ; Catalog Number: 0400-750-000 Sterile personal protection garment
    Category
    Medical Device
    Distribution
    Distributed nationwide