The Recall Desk

State

American Samoa product recalls

73,509 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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25726–25750 of 73534

  • CriticalFDA (Drugs)·D-0256-2021·2021-02-24

    Optimus Lubricants Instant Hand Sanitizer Recalled for Methanol Contamination

    Liq-E S.A. De C.V. is recalling Optimus Lubricants Instant Hand Sanitizer because the product contains methanol and has lower ethanol content than labeled.

    Product
    OPTIMUS LUBRICANTS Instant Hand Sanitizer, (alcohol 70% v/v) 275 Gal (1040 L) tank with spout dispenser, Made in Mexico, Liq-E, S.A. DE C.V., Puerto Tampico No. 345 Col. La Fe San Nicolas de Los Garza, Nuevo Leon, Mexico. C.P. 66477.; UPC # 7 501799 118981
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0254-2021·2021-02-24

    Liq-E Recalls Optimus Hand Sanitizer Due to Methanol Contamination

    Liq-E S.A. De C.V. is recalling 575 drums of Optimus Instant Hand Sanitizer because the product contains methanol and has lower ethanol content than labeled.

    Product
    OPTIMUS LUBRICANTS Instant Hand Sanitizer, (alcohol 70% v/v) 55 Gal (208 L) drum, Made in Mexico, Liq-E, S.A. DE C.V., Puerto Tampico No. 345 Col.. La Fe San Nicolas de Los Garza, Nuevo Leon, Mexico. C.P. 66477.UPC # 7 501799 118998
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1114-2021·2021-02-24

    Combat Medical Systems Recalls Fresh Whole Blood Donor Sets

    Combat Medical Systems is recalling 954 Fresh Whole Blood Donor Sets due to a potential bent or disconnected needle in the kit components.

    Product
    Fresh Whole Blood Donor Set (P/N 80-801-D NSN 6515016640306) . Blood convenience kit. The Fresh Whole Blood Doner Set contains everything needed to test for ABO/Rh compatibility and collect the whole blood from donor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V107000·2021-02-24

    Lamborghini Recalls Aventador SVJ Vehicles Due to Hood Hinge Defect

    Lamborghini is recalling 2018-2021 Aventador SVJ vehicles because hood hinge screws may loosen, potentially causing the hood to detach at high speeds.

    Product
    LAMBORGHINI — LAMBORGHINI AVENTADOR SVJ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1113-2021·2021-02-24

    Combat Medical Systems Recalls Fresh Whole Blood Transfusion Sets

    Combat Medical Systems is recalling Fresh Whole Blood Transfusion Sets due to a potential for bent or disconnected needles in the kit components.

    Product
    Fresh Whole Blood Transfusion Set (P/N 80-801 NSN 6515016574750) . Blood convenience kit. The Fresh Whole Blood Transfusion Set contains everything needed to test for ABO/Rh compatibility and perform a fresh whole blood transfusion in a compact sealed package.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1112-2021·2021-02-24

    Combat Medical Systems Recalls Low Titer Type O FWB Transfusion Sets

    Combat Medical Systems, LLC is recalling 1021 units of Low Titer Type O FWB Transfusion Sets due to the potential for bent or disconnected needles in the components.

    Product
    Low Titer Type O FWB Transfusion Set (P/N 80-875 NSN 651501684994). Blood convenience kit. The Transfusion Set includes the items necessary to administer the collected blood to a patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1110-2021·2021-02-24

    Combat Medical Systems Recalls Valkyrie LTOWB Blood Collection Kits

    Combat Medical Systems is recalling 531 Valkyrie LTOWB blood collection kits due to a potential for bent or disconnected needles.

    Product
    Valkyrie LTOWB Collection (P/N 80-820, NSN 6515016862423). Blood collection convenience kit. The Valkyrie LTOWB Collection Set includes the items needed to allow for pre-screening to identify Low Titer Type O Donors as well as collect the blood from the donor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1111-2021·2021-02-24

    Combat Medical Systems Recalls Valkyrie LTOWB Blood Administration Kits

    Combat Medical Systems is recalling 953 Valkyrie LTOWB Administration Sets due to a potential for bent or disconnected needles.

    Product
    Valkyrie LTOWB Administration (P/N 80-821 NSN 6515016862401). Blood convenience kit. The Valkyrie LTOWB Administration Set contains the items needed to administer the blood to the patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V112000·2021-02-24

    2021 International LT Trucks Recalled for Potential Flywheel Detachment

    Certain 2021 International LT vehicles with Cummins X15 engines may have improperly torqued flywheel capscrews that could detach during operation, causing loss of drive power and risk of ejected engine parts.

    Product
    INTERNATIONAL — INTERNATIONAL LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1109-2021·2021-02-24

    BD 10 ml Syringes Recalled for Potential Open Seals and Sterility Compromise

    Becton Dickinson is recalling 155,200 10 ml syringes because open packaging seals may compromise sterility. The product was distributed in the US and Canada.

    Product
    BD Hypodermic Syringe 10 ml, eccentric tip. Catalog (Ref No.) 305482
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1126-2021·2021-02-24

    Confirm Biosciences Recalls Orient Gene COVID-19 Rapid Test Cassettes

    Confirm Biosciences is recalling Orient Gene COVID-19 Rapid Test Cassettes because they were distributed outside Emergency Use Authorization and not validated for fingerstick use.

    Product
    Orient Gene COVID- 19 IgG/ IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) REF GCCOV-402a - Product Usage: is a lateral flow immunoassay intended for the qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV- 2 in human venous whole blood, plasma…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21087·2021-02-24

    Urban Outfitters Recalls Margo Taper Candle Holders Due to Fire Hazard

    Urban Outfitters is recalling Margo Taper Candle Holders because they can catch fire if they contact the flame. One fire incident was reported, with no injuries.

    Product
    Margo Taper Candle Holders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1124-2021·2021-02-24

    Getinge CM320 Washer Disinfector Recalled for Hose Deformation Risk

    Getinge is recalling CM320 Series Washer Disinfectors because plastic inlet hose connections may deform or break, potentially causing water leaks and burns.

    Product
    Getinge CM320 Series Washer Disinfector - Product Usage: A multi chamber washer disinfector intended for washing, disinfecting and drying of surgical instruments, containers, operating theatre shoes and operating theatre accessories normally used in hospitals and central…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1131-2021·2021-02-24

    Biomet Recalls Mislabelled 25mm Shoulder Prosthesis Central Screws

    Biomet is recalling 49 units of 25mm central screws for shoulder prostheses because they were mislabeled as 25mm but are actually 40mm.

    Product
    Central Screw 6.5x25mm - Product Usage: used as a sterile screw that is intended for implantable shoulder prosthesis assembly and/or fixation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V110000·2021-02-24

    2021-2022 Polestar 2 vehicles recalled for battery control software glitch

    Polestar is recalling certain 2021-2022 Polestar 2 vehicles. A software issue in the Battery Energy Control Module may cause the high voltage system to disconnect, resulting in loss of drive power and increased crash risk.

    Product
    POLESTAR — POLESTAR POLESTAR 2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21086·2021-02-24

    Northern Tool Recalls Powerhorse Generators Due to Electrical Shock Hazard

    Northern Tool & Equipment is recalling Powerhorse 13000ES portable generators due to a wiring error that can cause electrical shock. No injuries have been reported.

    Product
    Northern Tool & Equipment Powerhorse 13000ES Portable Generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1129-2021·2021-02-24

    GE Healthcare Recalls Revolution CT Systems Due to Table Pinch Protector Issue

    GE Healthcare is recalling 96 Revolution CT systems because a damaged or missing table pinch protector may expose sharp screws, posing a laceration risk.

    Product
    System, X-Ray, Tomography, Computed: Revolution Apex, Revolution CT with Apex Edition
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1130-2021·2021-02-24

    GE Healthcare Recalls Revolution CT Systems Due to Table Pinch Protector Defect

    GE Healthcare is recalling Revolution CT and Revolution CT ES systems because damaged or missing table pinch protectors may expose sharp screws, posing a laceration risk.

    Product
    System, X-Ray, Tomography, Computed: Revolution CT, Revolution CT ES.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21085·2021-02-24

    Potter Electric Recalls Addressable Pull Stations Due to Fire Alarm Failure

    Potter Electric is recalling specific addressable pull stations because the handle may fail to activate the fire alarm, posing a risk of failure to alert occupants to a fire.

    Product
    Potter Electric Addressable Pull Stations Single/Dual Action
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V108000·2021-02-24

    Freightliner Custom XC Chassis Recalled for Missing Brake Return Spring

    Daimler Trucks North America is recalling 2021-2022 Freightliner Custom XC Chassis vehicles because a missing brake pedal return spring may cause brake lights to stay on or brakes to remain engaged.

    Product
    FCCC — FCCC XC CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V111000·2021-02-24

    Audi A8 and S8 Engine Control Module Connector Defect May Cause Engine Stall

    Audi is recalling certain 2019-2021 A8 and 2020-2021 S8 vehicles due to a missing sealing pin on the engine control module connector. Moisture can enter the connector and cause the engine to stall, increasing crash risk.

    Product
    AUDI — AUDI S8, A8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1116-2021·2021-02-24

    Medtronic Recalls Cerebrospinal Fluid Valves Due to Radiopaque Marking Issues

    Medtronic Neurosurgery is recalling 22,528 units of STRATA II cerebrospinal fluid valves and shunts worldwide because radiopaque markings may vary in visibility under imaging.

    Product
    Medtronic Cerebro Spinal Fluid Flow Control Valves and Shunts. STRATA II Valves and Shunts for the following CFNs: 27739 - SHUNT 27739 STRATA NSC SNAP SML 120CM, 27740 - SHUNT 27740 STRATA NSC SNAP REG 120CM, 27812 - VALVE 27812 STRATA II SM EXTRACTED, 27814 - SHUNT…
    Category
    Medical Device
    Distribution
    Distributed nationwide