The Recall Desk

State

American Samoa product recalls

72,971 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 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6551–6575 of 72996

  • ModerateFDA (Devices)·Z-1719-2025·2025-05-14

    Meridian Bioscience ImmunoCard STAT! Crypto/Giardia Test Kits Recalled

    One lot of Meridian Bioscience ImmunoCard STAT! Crypto/Giardia Test Kits (Model 750830) was stored at improper temperatures in Medline warehouses. The test kits may not perform as intended due to storage outside labeled requirements.

    Product
    Meridian Bioscience ImmunoCard STAT! Crypto/Giardia Test Kits, Model Number 750830
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0410-2025·2025-05-14

    Homeopathic Oral Spray Temper Tamer Recalled for CGMP Deviations

    Siddha Flower Essences is voluntarily recalling Temper Tamer homeopathic oral spray due to Current Good Manufacturing Practice (CGMP) deviations identified during manufacturing.

    Product
    temper tamer, 1 US fl oz. (29.6 mL), Homeopathic Oral Spray, Manufactured by: Siddha Flower Essences, Oxnard, CA, 93030 NDC 69779-020-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0412-2025·2025-05-14

    Testosterone Pellet 100 mg recalled due to glass particle contamination

    BSO LLC is recalling Testosterone Pellet 100 mg (compounded, office use only) distributed nationwide due to glass particles found in pellet vials.

    Product
    TESTOSTERONE PELLET 100 mg (with Cholesterol </=4%), 1 Pellet for Subcutaneous Use, This is a Compounded Drug, Not for Resale, RX or Office Use Only, Belmar Select Outsources, 12860 W. Cedar Drive #211, Lakewood, CO 80228, NDC: 70168-0101-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1732-2025·2025-05-14

    B Braun Interventional Coaxial Dilator Micro-Introducer Kits Recall

    Galt Medical Corporation is recalling B Braun Interventional Coaxial Dilator Micro-Introducer Kits due to a potential open seal in the sterile barrier packaging. The affected kits are distributed nationwide in eight U.S. states and six countries.

    Product
    B Braun Interventional Coaxial Dilator REF: KIT-018-47, KIT-019-67, KIT-018-41, KIT-019-37 These Micro-Introducer Kits are intended to introduce up to a .038 inch guidewire or catheter into the vascular system following a small gauge needle stick.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1721-2025·2025-05-14

    Washer Disinfector Aquadis 56 Model 56M Recalled

    Getinge Disinfection Ab recalls the Washer Disinfector Aquadis 56 (Model 56M) because the frequency inverter is not programmed to specification, causing the circulation pump to start earlier than expected and wear the axial seal prematurely.

    Product
    Washer Disinfector Aquadis 56; Model Number: 56M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1729-2025·2025-05-14

    Philips Tempus Pro Patient Monitor Software Update for Operational Issues

    Remote Diagnostic Technologies Ltd. is issuing a software update for the Philips Tempus Pro Patient Monitor due to freezing, rebooting, and potential ECG measurement accuracy issues across multiple software versions.

    Product
    Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, 00-1007
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1718-2025·2025-05-14

    Bio 1 Granules for Filling implant bone graft material nationwide recall

    Bio 1 Granules for Filling implant bone granules may contain less product than specified on the label. The affected lot is 240781 (UDI: 03760154000369), distributed nationwide.

    Product
    Bio 1 Granules for Filling ¿ 1 mm (2 cm¿), REF:P822692243, Material: BIOSORB (BTCP 95% minimum purity)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1734-2025·2025-05-14

    GALT Guidewire SGW-051-07 Sterile Packaging Seal Defect Recall

    Galt Medical Corporation is recalling GALT Guidewire model SGW-051-07 due to a potential open seal in the sterile barrier packaging. The defect may compromise the sterility of the device.

    Product
    GALT Guidewire REF SGW-051-07 Guidewires are intended for use in percutaneous procedures, to introduce and position catheters and other interventional devices within the Coronary and peripheral vasculature.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1723-2025·2025-05-14

    Ambu aScope 5 Broncho HD Endoscope Labeling Error Recall

    Ambu Inc. is recalling 160 units of the Ambu aScope 5 Broncho HD 5.6/2.8 Sampler Set due to incorrect front pouch labeling that states 5.0/2.2 instead of the correct size 5.6/2.8.

    Product
    Ambu aScope" 5 Broncho HD 5.6/2.8 Sampler Set. Model Number: 622002000US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1738-2025·2025-05-14

    Blueprint Software version 4.2.1 surgical planner access bug

    Tornier's Blueprint Software version 4.2.1 contains a bug that prevents surgeons from accessing surgical cases created in earlier software versions.

    Product
    Blueprint Software, BPUE001. Intended for use by surgeons as a pre surgical planner for shoulder replacement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0403-2025·2025-05-14

    Timolol Maleate Ophthalmic Solution Recalled for Defective Container

    FDC Limited is recalling Timolol Maleate Ophthalmic Solution 0.5% due to a defective container where the spike of the cap becomes lodged in the bottle nozzle, preventing users from accessing the solution.

    Product
    TIMOLOL MALEATE — TIMOLOL MALEATE (TIMOLOL MALEATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1724-2025·2025-05-14

    INSPIRA AIR Balloon Dilation System packaging error corrected nationwide

    Integra LifeSciences is recalling INSPIRA AIR Balloon Dilation System 10x40 cartons because an incorrect product was packaged inside. The recall affects six units distributed across Texas, Montana, Alabama, and Oklahoma.

    Product
    INSPIRA AIR BALLOON DILATION SYSTEM 10x40, 1 PK. Airway balloon dilation catheter.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1720-2025·2025-05-14

    Washer Disinfector Aquadis 56 Model 56A pump seal defect recall

    Getinge Disinfection Ab is recalling Washer Disinfector Aquadis 56 (Model 56A) units due to a frequency inverter programming error that causes the circulation pump to start earlier than expected, leading to accelerated wear on the axial seal.

    Product
    Washer Disinfector Aquadis 56; Model Number: 56A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V215000·2025-05-13

    Mitsubishi Fuso Recalls 2024 Rizon Trucks for Turn Signal Defect

    Mitsubishi Fuso is recalling 243 2024 Rizon trucks because a defective bulb socket may cause front turn signals to burn out, increasing crash risk.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO RIZON FEC7K (E16), RIZON FEC9K (E18)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V255000·2025-05-12

    Mercedes-Benz Recalls Vehicles With Incorrect Fuse Boxes From Prior Repair

    Mercedes-Benz is recalling 443 vehicles that received an incorrect fuse box during a previous recall. The defect may cause loss of drive power, safety functions, or fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH AMG EQS 53 4MATIC, AMG SL55 4MATIC+, AMG EQE 53 4MATIC, AMG SL63 4MATIC+
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E034000·2025-05-12

    Waymo Recalls 5th Generation Automated Driving Systems for Collision Risk

    Waymo is recalling 5th Generation Automated Driving Systems with older software that may cause vehicles to collide with roadway barriers like chains and gates.

    Product
    ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V317000·2025-05-12

    ATC Recalls 2025 PLA550 Trailers Due to Wiring Fire Risk

    ATC is recalling 2025 PLA550 Bumper Pull trailers because the power wire to stabilizer jacks may lack over-current protection, increasing fire risk.

    Product
    ATC — ATC PLA550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V310000·2025-05-09

    Ford Bronco upper control arm ball joint fasteners may be missing

    Ford is recalling certain 2024-2025 Bronco and Ranger vehicles because the front upper control arm ball joint fastener may be missing or improperly tightened.

    Product
    FORD — FORD BRONCO, RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V308000·2025-05-09

    Ford Bronco lower control arms may detach; owners told not to drive

    Ford is recalling certain 2024-2025 Bronco vehicles because front lower control arm fasteners may not be tightened, allowing the arm to detach. Owners are told not to drive.

    Product
    FORD — FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V314000·2025-05-09

    Ford Expedition front brake lines may contact the air cleaner pipe

    Ford is recalling certain 2022-2024 Expedition and Lincoln Navigator vehicles because front brake lines may contact the engine air cleaner outlet pipe and leak brake fluid.

    Product
    FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V309000·2025-05-09

    Ford Recalls 2025 F-150 Trucks for Steering Shaft Fastener Defect

    Ford is recalling 2025 F-150 vehicles because lower steering shaft fasteners may detach, causing loss of steering control and increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V316000·2025-05-09

    Ford Explorer front subframe mounting bolts may be improperly tightened

    Ford is recalling certain 2025 Explorer and Lincoln Aviator vehicles because a mounting bolt for the front subframe may have been tightened improperly. 206 units affected.

    Product
    LINCOLN — LINCOLN, FORD AVIATOR, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V303000·2025-05-09

    Ford Bronco rear doors may open despite the child safety lock

    Ford is recalling certain 2024 Bronco vehicles because the left-side rear door may be opened from inside the vehicle when the child safety lock is in the ON position.

    Product
    FORD — FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V312000·2025-05-09

    Ford Bronco rearview image may persist after the backing event ends

    Ford is recalling certain 2021-2022 Bronco vehicles repaired incorrectly under recall 22V-825, because the rearview camera image may still display after backing has ended.

    Product
    FORD — FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide