The Recall Desk

State

American Samoa product recalls

72,940 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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5076–5100 of 72965

  • SevereNHTSA·25V648000·2025-09-25

    Bentley high pressure fuel pump joint may be improperly tightened

    Bentley is recalling certain 2025-2026 Continental GT, Continental GTC and 2025 Flying Spur vehicles because the bolted joint securing the high-pressure fuel pump to the V8 engine may be improperly tightened.

    Product
    BENTLEY — BENTLEY CONTINENTAL GT, FLYING SPUR, CONTINENTAL GT CABRIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V647000·2025-09-25

    International Recalls 2025-2026 IC Bus CECB Due to Parking Brake Defect

    International is recalling 2025-2026 IC Bus CECB commercial buses because a tire may damage an air line, causing the parking brake to activate unintentionally while driving.

    Product
    IC BUS — IC BUS CECB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·PHA-09252025-01·2025-09-25

    USDA Alerts on Ready-to-Eat Pasta Meals Linked to Listeria Outbreak

    USDA FSIS issued a public health alert for specific ready-to-eat pasta meals sold at Walmart and Trader Joe's due to possible Listeria monocytogenes contamination linked to a confirmed outbreak.

    Product
    Freshrealm — FSIS Issues Public Health Alert For Ready-To-Eat Meals Containing Pasta That May Be Contaminated with Listeria
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V642000·2025-09-25

    Jeep Wagoneer quarter window trim may not be properly secured

    Chrysler is recalling certain 2022-2024 Jeep Wagoneer and Grand Wagoneer vehicles because the quarter trim on the driver and passenger windows may not have been properly secured and can detach.

    Product
    JEEP — JEEP WAGONEER, GRAND WAGONEER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V641000·2025-09-25

    International Recalls 2026 IC Bus CECB for Wiper Crank Shaft Defect

    International is recalling 2026 IC Bus CECB commercial buses because a weld on the wiper crank shaft may fail, causing the left-side wiper to stop working.

    Product
    IC BUS — IC BUS CECB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V650000·2025-09-25

    Altec Recalls Aerial Devices Due to Outrigger Pad Fire Risk

    Altec is recalling 2021-2025 aerial devices because the outrigger pad holder may be installed too close to the exhaust, increasing fire risk.

    Product
    ALTEC — ALTEC AN SERIES AERIAL DEVICE, AM SERIES AERIAL DEVICE, AA SERIES AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V639000·2025-09-25

    Chevrolet Equinox EV pedestrian alert sound may be insufficient

    General Motors is recalling certain 2024 Chevrolet Equinox EV vehicles because the pedestrian alert sound system may not change volume enough between standstill and low speed, failing FMVSS 141.

    Product
    CHEVROLET — CHEVROLET EQUINOX EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V645000·2025-09-25

    Range Rover Evoque rearview camera can admit water distorting the image

    Land Rover is recalling certain 2023 Range Rover Evoque vehicles because water may enter the rearview camera, so the image may not appear on the display or may appear distorted.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25477·2025-09-25

    Numbing cream recalled because lidocaine packaging is not child resistant

    About 28,000 RELIEVE numbing cream containers are recalled because the lidocaine product is not in child-resistant packaging as required by the Poison Prevention Packaging Act. No incidents reported.

    Product
    RELIEVE Numbing Cream
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V649000·2025-09-25

    Kia Sorento blower motor wiring harness may be inadequate causing fire

    Kia is recalling certain 2021-2023 Sorento vehicles because the heating, ventilation and air conditioning blower motor wiring harness may be inadequate, which can result in a fire.

    Product
    KIA — KIA SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25C010000·2025-09-25

    Evenflo Recalls Revolve360 Slim Child Seats Due to Foam Choking Hazard

    Evenflo is recalling Gold Revolve360 Slim and Revolve360 Slim child seats because loose headrest foam can break off and pose a choking hazard to children.

    Product
    CHILD SEAT:SHELL:HEADREST recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0655-2025·2025-09-24

    Cyclobenzaprine bottles recalled after being filled with meloxicam tablets instead

    Unichem Cyclobenzaprine Hydrochloride Tablets, 10 mg, lot GMML24026A, are recalled because bottles labeled as cyclobenzaprine contained yellow Meloxicam 7.5 mg tablets. The FDA classified the action as Class I.

    Product
    CYCLOBENZAPRINE HYDROCHLORIDE — CYCLOBENZAPRINE HYDROCHLORIDE (CYCLOBENZAPRINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2483-2025·2025-09-24

    Blood and fluid warming sets recalled to clarify flow rates and temperatures

    3M Ranger Blood/Fluid Warming High Flow Sets are the subject of a field action to clarify flow rates, inlet fluid temperatures and the location of the outlet temperature. The FDA classified it as Class I.

    Product
    3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355, 24370
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V638000·2025-09-24

    Volkswagen and Audi front seat belt retractor torsion bars may be damaged

    Volkswagen is recalling certain 2025-2026 GTI, Golf R, Audi A5, S5, A6 and Q4 e-Tron models because the torsion bar in one or both front seat belt retractors may have been damaged during production.

    Product
    AUDI — AUDI, VOLKSWAGEN Q4 E-TRON, A6 SPORTBACK E-TRON, S5, S6 SPORTBACK E-TRON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V637000·2025-09-24

    Audi SQ7 high pressure fuel pump fasteners may be loose

    Volkswagen is recalling one Audi SQ7 vehicle because the fasteners securing the high pressure fuel pump may not be tightened properly, resulting in a fuel leak. The vehicle has been repaired.

    Product
    AUDI — AUDI SQ7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E059000·2025-09-24

    Lippert Paddle Latches Recalled for Risk of LP Compartment Fire

    Lippert is recalling specific paddle latches used on REV Recreation Group vehicles because they may lock unintentionally, preventing access to the liquid propane compartment and increasing fire risk.

    Product
    LATCHES/LOCKS/LINKAGES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2564-2025·2025-09-24

    CD20 reagent lots recalled over weak staining risking false negative identification

    FLEX Monoclonal Mouse Anti-Human CD20cy for Dako Omnis, catalog GA60461-2CN, is recalled because of the potential for weak staining that may result in false negative CD20 identification. 65 units are affected.

    Product
    Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use (Dako Omnis) Model/Catalog Number: GA60461-2CN Software Version: Not applicable Product Description: FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use (Dako Omnis) is intended for use i
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2570-2025·2025-09-24

    Radiation planning software recalled over image errors in three patient orientations

    Pinnacle Radiation Therapy Planning System software is recalled because of a potential image error of the Region of Interest for expansion or contraction in head first prone, feet first supine and feet first prone orientations.

    Product
    Pinnacle Radiation Therapy Planning System: Multimodality Simulation Workspace 18.0.5 Model 870258 UDI code: (01)00884838103566(10)18.0.5.22236 Pinnacle TumorLOC 16.2 Model 870226 UDI code: (01)00884838091122(10)16.2.0.60010 Pinnacle TumorLOC 16.2.1 Model 870227 UDI c
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2574-2025·2025-09-24

    DxH 800 hematology analyzers recalled over erroneously high hemoglobin results

    UniCel DxH 800 Coulter Cellular Analysis Systems configured with the LED HGB photometer are recalled because they may produce erroneously high hemoglobin results on samples with elevated white blood cell counts.

    Product
    UniCel DxH 800 COULTER Cellular Analysis System, configured with the Led HGB Photometer REFs:B24802, 629029, B63322
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2572-2025·2025-09-24

    DxH 900 hematology analyzers recalled over erroneously high hemoglobin results

    UniCel DxH 900 Coulter Cellular Analysis Systems configured with the LED HGB photometer are recalled because they may produce erroneously high hemoglobin results on samples with elevated white blood cell counts.

    Product
    UniCel DxH 900 COULTER Cellular Analysis System, configured with the Led HGB Photometer REF: C11478
    Category
    Medical Device
    Distribution
    Distributed nationwide