The Recall Desk

State

American Samoa product recalls

73,198 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
5
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 5 (20%) are Severe.

Which agencies issued them

These figures cover only the 25 recalls whose distribution notice names American Samoa specifically. The 73,198 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15926–15950 of 73223

  • ModerateFDA (Drugs)·D-0759-2023·2023-05-31

    Glimepiride 4 Milligram Tablets Nationwide Recalled for Manufacturing Practice Deviations

    Amerisource Health Services LLC is recalling 129,849 bottles of Glimepiride Tablets, USP 4 mg nationwide due to manufacturing practice deviations identified during an FDA inspection. No illnesses have been reported.

    Product
    Glimepiride Tablets, USP, 4 mg, RX, Packaged as a) 100-count bottle, NDC# 68001-179-00; b) 500-count bottle, NDC# 68001-179-03, Manufactured by: Intas Pharmaceuticals Limited, Pharmez, Ahmedabad-382 213. INDIA. For BluePoint Laboratories
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1479-2023·2023-05-31

    Fluoroscopic imaging system may display incorrect radiation dose readings

    Siemens Luminos Agile Max fluoroscopic imaging systems may occasionally display incorrect radiation dose information under certain unlikely circumstances. The manufacturer states there is no impact on clinical workflow or diagnosis. The error only occurs in systems with a second overhead X-ray tube.

    Product
    Luminos Agile Max (VE10, VF10, VF11)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1632-2023·2023-05-31

    Siemens Atellica CH Toxicology Calibrator Reassignment Due to Positive Bias

    Siemens Healthcare Diagnostics is reassigning Atellica CH Toxicology Calibrators due to a positive bias. The affected calibrators were distributed in the US and internationally across multiple countries.

    Product
    Atellica CH Toxicology Calibrator (TOX CAL)-The Atellica¿ CH Toxicology Calibrator (TOX CAL) is for in vitro diagnostic use in calibrating the Acet, ETOH and Sal assays using the Atellica¿ CH Analyzer Siemens Material Number (SMN): 11099440
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0767-2023·2023-05-31

    Fentanyl Buccal Tablets Recalled for Missing or Incorrect Package Insert

    Teva Pharmaceuticals is recalling Fentanyl Buccal Tablets (200mcg) due to missing or incorrect package inserts. Patients should contact their healthcare provider if they have affected product.

    Product
    Fentanyl Buccal Tablets CII, 200mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-635-28
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1480-2023·2023-05-31

    Fluoroscopic Imaging System May Display Incorrect Radiation Dose Measurements

    Siemens Luminos dRF Max fluoroscopic imaging systems may occasionally display incorrect radiation dose measurements during certain operating conditions. The manufacturer states the error does not affect diagnosis or workflow.

    Product
    Luminos dRF Max (VE10, VF10, VF11)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1481-2023·2023-05-31

    LUMINOS Lotus Max fluoroscopic system recalled for sporadic measurement errors

    LUMINOS Lotus Max fluoroscopic systems may sporadically display incorrect radiation dose measurements. The error only occurs with secondary X-ray tubes and does not affect diagnosis or workflow.

    Product
    LUMINOS Lotus Max (VF11)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0757-2023·2023-05-31

    Nationwide Recall of Glimepiride Tablets for Manufacturing Practice Deviations

    Amerisource Health Services LLC recalls 63,335 bottles of Glimepiride Tablets nationwide due to manufacturing practice deviations identified during FDA inspection.

    Product
    Glimepiride Tablets, USP, 1 mg, RX, Packaged as a)100-count bottle, NDC# 68001-177-00; b) 500-count bottle, NDC# 68001-177-03; Manufactured by: Intas Pharmaceuticals Limited, Pharmez, Ahmedabad-382 213. INDIA. For BluePoint Laboratories
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0770-2023·2023-05-31

    Fentanyl buccal tablets recalled due to incorrect or missing package insert

    Teva Pharmaceuticals USA Inc is recalling Fentanyl Buccal Tablets 800mcg due to incorrect or missing package inserts. The recall affects 3,032 units distributed nationwide.

    Product
    Fentanyl Buccal Tablets CII, 800mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-638-28
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0766-2023·2023-05-31

    Fentanyl Buccal Tablets recalled due to missing or incorrect package insert

    Teva Pharmaceuticals is recalling Fentanyl Buccal Tablets 100mcg due to incorrect or missing package inserts in affected cartons. Patients should verify proper labeling or contact their pharmacy.

    Product
    Fentanyl Buccal Tablets CII, 100mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-634-28
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0769-2023·2023-05-31

    Fentanyl Buccal Tablets 600mcg Recalled for Incorrect or Missing Package Insert

    Teva Pharmaceuticals is recalling Fentanyl Buccal Tablets 600mcg due to incorrect or missing package inserts in 1,908 units distributed nationwide across multiple lot numbers.

    Product
    Fentanyl Buccal Tablets CII, 600mcg, packaged in cartons of 28 Buccal Tablets (4 tablets x 7 cards), Rx only, Distributed by: Mayne Pharma, Greenville, NC 27834, NDC 51862-637-28
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0756-2023·2023-05-31

    Methylprednisolone Acetate Injectable Suspension recalled for NDC carton labeling error

    Amneal Pharmaceuticals recalls Methylprednisolone Acetate Injectable Suspension due to incorrect NDC number on product cartons. The typographical error appears on secondary packaging only; the medication vial itself is unaffected.

    Product
    Methylprednisolone Acetate Injectable Suspension, USP 80 mg/mL, For Intramuscular, Intrasynovial and Soft Tissue Injection Only, Not for Intravenous Use, 1 mL Single Dose Vial, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd. Parenteral Unit, Ahmedabad 382213, India, Amneal…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V382000·2023-05-30

    Alfa Romeo Giulia and Stelvio Recalled for Brake Rotor Fracture Risk

    NHTSA is recalling 2017-2020 Alfa Romeo Giulia and 2018-2020 Stelvio vehicles with carbon ceramic brakes due to a risk of rotor fracture and decreased brake performance.

    Product
    ALFA ROMEO — ALFA ROMEO GIULIA, STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V384000·2023-05-30

    2023 Toyota Corolla Cross instrument panel airbag deployment risk

    Toyota is recalling 2022-2023 Corolla Cross vehicles because the instrument panel may lack required perforations, preventing proper front-passenger airbag deployment in a crash.

    Product
    TOYOTA — TOYOTA COROLLA CROSS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V378000·2023-05-26

    Ford Recalls 2015-2019 Lincoln MKC for Engine Compartment Fire Risk

    Ford is recalling 2015-2019 Lincoln MKC vehicles because a battery monitor sensor may short-circuit and overheat, causing a fire in the engine compartment.

    Product
    LINCOLN — LINCOLN MKC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V375000·2023-05-26

    Forest River Recalls 2023 East to West Travel Trailers Due to Gas Leak Risk

    Forest River is recalling 2023 East to West Della Terra and Silver Lake travel trailers because an incorrectly installed furnace may cause a gas leak inside the cabin.

    Product
    EAST TO WEST — EAST TO WEST DELLA TERRA, SILVER LAKE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V381000·2023-05-26

    Knapheide Recalls Vehicles with Warn Winches Due to Unintentional Operation Risk

    Knapheide is recalling 2022-2023 trucks equipped with certain Warn winches because water intrusion can cause the winch to operate unintentionally, increasing injury risk.

    Product
    KNAPHEIDE — KNAPHEIDE RAM 3500, FORD F-350, FORD F-250, FORD F-550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V380000·2023-05-26

    Ford Escape, Maverick, and Corsair Engine Fire Risk Recall

    Ford is recalling certain 2020-2023 Escape, 2022-2023 Maverick, and 2021-2023 Corsair vehicles due to a 2.5L engine defect that could cause an engine compartment fire. No injuries have been reported.

    Product
    FORD — FORD, LINCOLN MAVERICK, CORSAIR, ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V379000·2023-05-26

    Ford Vehicles Recalled for Incorrect Tire and Loading Capacity Label

    Ford is recalling certain 2019-2023 Ranger, 2022-2023 Bronco, and 2023 F-250 SD vehicles with TREAD labels stating incorrect load carrying capacity, which could result in vehicle overload and increase crash risk.

    Product
    FORD — FORD F-250 SD, RANGER, BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V376000·2023-05-26

    Travel trailers recalled for missing wardrobe cabinet backer board

    Certain 2021-2023 Keystone Arcadia travel trailers lack a backer board behind the wardrobe cabinet, potentially allowing the slide room to extend and cause injury. Dealers will install steel brackets to secure the slide room at no cost.

    Product
    KEYSTONE — KEYSTONE ARCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V373000·2023-05-25

    2021-2023 Autocar Xpeditor trucks recalled for defective door latch

    Autocar is recalling 2021-2023 Xpeditor commercial trucks due to incorrectly assembled right-side door latches that may open unexpectedly during operation. Owners should contact Autocar for a free inspection and reassembly.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V369000·2023-05-25

    Jaguar I-PACE Battery Overheat May Increase Fire Risk

    Jaguar is recalling certain 2019-2024 I-PACE vehicles because the high-voltage battery may overheat, increasing the risk of fire. Owners should park and charge vehicles outside until repairs are complete.

    Product
    JAGUAR — JAGUAR I-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V368000·2023-05-25

    Fontaine Recalls 2023-2024 Container Trailers Due to Missing Reflectors

    Fontaine Trailer Company is recalling 2023-2024 40-foot container trailers because they may be missing rear reflex reflectors, which reduces visibility and increases crash risk.

    Product
    FONTAINE — FONTAINE CONTAINER TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide