The Recall Desk

State

American Samoa product recalls

73,104 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 73,104 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12576–12600 of 73129

  • HighFDA (Devices)·Z-1012-2024·2024-02-14

    BD antibiotic susceptibility testing discs recalled for accuracy failures

    Becton Dickinson is recalling BD BBL Sensi Disc Ampicillin antibiotic susceptibility testing discs due to accuracy and quality control failures that may cause delayed diagnosis or inappropriate antibiotic selection.

    Product
    BD BBL Sensi Disc Ampicillin - 10 ¿g, Catalog No. 230705 and 231264; 2 ¿g, Catalog No. 231263. Used for semi-quantitative in vitro susceptibility testing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1038-2024·2024-02-14

    BD BBL Sensi Disc Rifampin Antibiotic Susceptibility Test Discs Recalled

    BD BBL Sensi Disc Rifampin antibiotic susceptibility test discs are being recalled due to potential accuracy and quality control failures. These discs are distributed domestically nationwide and internationally.

    Product
    BD BBL Sensi Disc Rifampin- 5 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231541 and 231544¿
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0314-2024·2024-02-14

    Prescription Drug Febuxostat Recalled Due to Manufacturing Practice Violations

    Amerisource Health Services LLC is recalling approximately 1,932 cartons of Febuxostat (40 mg tablets) nationwide due to deviations from current good manufacturing practices. The firm initiated the recall voluntarily on January 25, 2024.

    Product
    FEBUXOSTAT — FEBUXOSTAT (FEBUXOSTAT)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0312-2024·2024-02-14

    FDA Recalls Glimepiride Tablets for Misprint on Tablet

    Dr. Reddy's Laboratories is recalling Glimepiride 1mg tablets due to a misprint on the tablet. The recall affects 59,336 bottles distributed nationwide.

    Product
    GLIMEPIRIDE — GLIMEPIRIDE (GLIMEPIRIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0313-2024·2024-02-14

    Prescription Glimepiride Tablets Recalled Due to Tablet Misprint

    Dr. Reddy's Laboratories is recalling Glimepiride 1mg tablets nationwide due to a printing defect on the tablet. The voluntary recall affects 14,425 bottles.

    Product
    GLIMEPIRIDE — GLIMEPIRIDE (GLIMEPIRIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0856-2024·2024-02-14

    Popcorn Pre-Pop Recalled Due to Undeclared Yellow #5 Dye

    County Fair Foods is recalling 42,000 bags of Popcorn Pre-Pop nationwide due to undeclared Yellow #5 dye. The voluntary recall was initiated because Yellow #5 was not declared on the product label.

    Product
    Popcorn Pre-Pop in 8oz Polypropylene bag packaged 20 bags to a case
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0315-2024·2024-02-14

    Medline Antifungal Cream Recalled for False Paraben-Free Labeling

    Medline Remedy Clinical antifungal cream is recalled for labeling that falsely claims to be paraben-free while the product actually contains parabens. About 1,786 tubes nationwide are affected.

    Product
    MEDLINE — MEDLINE (MICONAZOLE NITRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0859-2024·2024-02-14

    Phosphatidyl Serine Softgels Recalled for Understated Ingredient Concentration

    Now Foods has recalled Phosphatidyl Serine 300mg softgels due to lower actual ingredient content than labeled. The recall affects 12,051 bottles distributed nationwide and internationally.

    Product
    Protocol for Life Balance, Phosphatidyl Serine 300mg softgels, 50 count bottle, UPC 707359123922. NOW Foods, Phosphatidyl Serine 300mg softgels, 50 count bottle, UPC 733739023926.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0320-2024·2024-02-14

    Hydralazine Hydrochloride Tablets Recalled Due to Failed Purity Tests

    Amerisource Health Services is recalling HydrALAZINE Hydrochloride Tablets (10 mg) due to failed impurity specifications discovered during 6-month stability testing.

    Product
    HydrALAZINE Hydrochloride Tablets, USP, 10 mg, 100-count (10 x 10) per unit dose carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 68084-447-01; NDC Unit Dose: 68084-447-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1004-2024·2024-02-14

    Olympus Paparella-Type Vent Tube Recall: Missing Expiration Date on Inner Packaging

    Olympus Corporation of the Americas is recalling one lot of Paparella-Type Vent Tubes due to missing expiration date on the inner package, though the date is present on the outer packaging.

    Product
    Olympus/Gyrus Paparrela-Type Vent Tube 1.02MM, Silicone, Sterile- to ventilate the middle ear subsequent to otitis media Model: 240044
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V107000·2024-02-13

    Hyundai Recalls Genesis Models Due to Starter Solenoid Fire Risk

    Hyundai is recalling certain 2015-2019 Genesis vehicles because water in the starter solenoid can cause an electrical short and engine fire.

    Product
    HYUNDAI — HYUNDAI, GENESIS GENESIS, G80, G90, G70
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24E014000·2024-02-13

    Dainese Recalls AGV Tourmodular Helmets Due to Buckle Failure Risk

    Dainese is recalling AGV Tourmodular helmets because the micrometric buckle may fail to engage, leaving the chin strap loose. This defect increases the risk of injury during a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V106000·2024-02-13

    2024 Hyundai Palisade Engine Valve Springs May Break While Driving

    Hyundai is recalling certain 2024 Palisade vehicles because engine valve springs may break while driving, potentially causing loss of drive power and engine block damage. This increases the risk of crashes and fires.

    Product
    HYUNDAI — HYUNDAI PALISADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24E013000·2024-02-13

    Waymo Recalls 5th Generation Automated Driving Systems for Software Defect

    Waymo is recalling 5th Generation Automated Driving Systems with software released before December 20, 2023, because the systems may inaccurately predict the movement of towed vehicles.

    Product
    ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V105000·2024-02-13

    Belmont FlatTrak Trailers Recalled for Spindle Mount Cracking Risk

    Belmont Trailers is recalling 2023-2024 FlatTrak trailers because the spindle mount may crack and separate, increasing the risk of a crash.

    Product
    BELMONT TRAILER — BELMONT TRAILER FLATRAK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V108000·2024-02-13

    2023 CFMOTO 450SS Motorcycle Telematics Box Fall May Cause Steering Loss

    CFMOTO is recalling certain 2023 450SS motorcycles where the telematics box may fall onto the steering forks, causing loss of steering control and increasing crash risk. Dealers will replace the T-box holder at no charge.

    Product
    CFMOTO — CFMOTO 450SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·006-2024·2024-02-12

    Fratelli Beretta Recalls Ready-to-Eat Charcuterie Due to Under Processing

    Fratelli Beretta USA is recalling ready-to-eat charcuterie products containing Coppa due to possible under processing and Salmonella contamination.

    Product
    Fratelli Beretta USA, INC. — Fratelli Beretta USA, Inc. Recalls Ready-To-Eat Charcuterie Meat Products Due to Possible Under Processing
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·24V104000·2024-02-12

    Integrated brake system malfunction in 2023-2025 BMW and MINI vehicles

    BMW is recalling certain 2023-2025 BMW, MINI, and Rolls-Royce vehicles due to integrated brake system malfunction. The defect may cause loss of power brake assist or ABS/DSC failure, increasing crash risk.

    Product
    BMW — BMW, MINI, ROLLS-ROYCE X7, 530I, 750E, 760I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V103000·2024-02-12

    Motorhomes recalled for LPG tank mounting bracket failure and fire risk

    Forest River recalled certain 2019-2024 Georgetown and FR3 motorhomes because LPG tank mounting brackets may break, allowing tanks to become dislodged and damaged, creating a fire risk. Dealers will replace the brackets at no charge.

    Product
    FOREST RIVER — FOREST RIVER GEORGETOWN, FR3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V097000·2024-02-09

    2021-2022 Ford E-350 and E-450 Power Steering Fluid Loss Recall

    Ford is recalling certain 2021-2022 E-350 and E-450 vehicles due to a defective power steering connection that may cause loss of power steering fluid and brake assist.

    Product
    FORD — FORD E-350, E-450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V098000·2024-02-09

    Vermeer Recalls BC1800XL Trailers Due to Tongue Weldment Crack Risk

    Vermeer is recalling 2016-2024 BC1800XL brush chipper trailers because the tongue weldment may crack and separate from the tow hitch, increasing crash risk.

    Product
    VERMEER — VERMEER BC1800XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E010000·2024-02-09

    R.H. Sheppard Recalls Steering Gears Due to Fracture Risk

    R.H. Sheppard is recalling steering gears where the sector shaft may have been improperly heat-treated, potentially causing cracks or fractures that lead to loss of steering control.

    Product
    STEERING:GEAR BOX:SHAFT SECTOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide