The Recall Desk

State

American Samoa product recalls

73,381 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 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20501–20525 of 73406

  • ModerateFDA (Devices)·Z-1224-2022·2022-06-08

    Medical Device Patient Interface Recalled Due to Software Anomaly

    Medtronic is recalling the NIM Vital Patient Interface 4.0 due to a software anomaly identified in the device. The recall affects 29 units distributed worldwide, including in the US and France.

    Product
    NIM Vital Patient Interface 4.0 (P/N: NIM4CPB1) NIM with Software version 1.3.2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0975-2022·2022-06-08

    Family Dollar AMBI Skincare Sunscreen Recalled for Improper Storage

    Family Dollar is recalling an AMBI Skincare Even & Clear Nourishing Daily Facial Moisturizer (SPF 30) for improper storage. The product may have reduced efficacy.

    Product
    Only At Family Dollar AMBI Skincare Even & Clear Nourishing Daily Facial Moisturizer With Broad Spectrum SPF 30 Sunscreen, Net Wt. 1.7 FL. OZ. (50 mL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1150-2022·2022-06-08

    Lumbar Tray with Swab Products Recalled Due to Manufacturing Validation Uncertainty

    Busse Hospital Disposables is recalling Lumbar Tray units nationwide because test methods used during manufacturing could not be adequately validated. The recall affects swab/swabstick products used in medical procedures.

    Product
    Lumbar Tray Catalog 1091
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0972-2022·2022-06-08

    Losartan Potassium tablets recalled for excessive AZIDO impurity

    Strides Pharma is recalling approximately 200,407 bottles of Losartan Potassium 25 mg tablets nationwide due to AZIDO impurity levels exceeding acceptable manufacturing limits.

    Product
    LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1164-2022·2022-06-08

    Busse Convenience Kits Swabs Recalled Due to Testing Validation Uncertainty

    Busse Hospital Disposables is recalling Busse Convenience Kits containing medical swabs and swabsticks due to uncertainty about test method validation in manufacturing. No illnesses reported.

    Product
    Pain Tray Catalog Number: 9883
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1159-2022·2022-06-08

    Single Shot Epidural Tray Recalled Due to Test Validation Uncertainty

    Single Shot Epidural Trays made by Busse Hospital Disposables are being recalled nationwide due to inadequate validation of the test methods used to manufacture the product. The recall affects 400 units.

    Product
    Single Shot Epidural Tray Catalog Number: 8417
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1146-2022·2022-06-08

    FDA recalls APD Drain Manifold units lacking regulatory clearance

    Baxter Healthcare is recalling 180 APD Drain Manifold units distributed in nine US states because certain product codes lack FDA regulatory clearance. Patients using affected units should contact Baxter Healthcare immediately.

    Product
    APD Drain Manifold
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1168-2022·2022-06-08

    Cervical Tray Recalled for Manufacturing Test Method Validation Uncertainty

    Busse Hospital Disposables is recalling Cervical Tray Catalog Number 3765R2 units containing swab products due to uncertainty about the adequacy of manufacturing test method validation. Lot Numbers 2031213S and 2130221S are affected.

    Product
    Cervical Tray Catalog Number: 3765R2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1151-2022·2022-06-08

    Busse Hospital Epidural Trays Recalled for Manufacturing Validation Uncertainty

    Busse Hospital Disposables is recalling Single Shot Epidural Trays due to uncertainty about whether manufacturing test methods were adequately validated. No illnesses or injuries have been reported.

    Product
    Single Shot Epidural Tray Catalog 1165
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1197-2022·2022-06-08

    Drug Swab Products Recalled for Manufacturing Validation Uncertainty

    Busse Convenience kits containing swab/swabstick drug products made by PDI are being recalled due to uncertainty about validation testing adequacy in manufacturing. Users should discontinue use of affected lot numbers.

    Product
    3.2MM Pellet Insertion Tray Catalog Number: B7345R1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V398000·2022-06-07

    C.E. Smith and Malone Auto Racks Recall Boat Trailers Due to Axle Weld Failure

    C.E. Smith is recalling 2021-2022 boat trailers because a weld may fail, causing the wheel to separate and increasing crash risk.

    Product
    MALONE AUTO RACKS — MALONE AUTO RACKS, C.E. SMITH COMPANY MICROSPORT MPG460, MULTI-SPORT 48810, ECOLIGHT MPG585, MULTI-SPORT 48815
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V400000·2022-06-07

    Off Grid Trailers Recalls 2021-2022 Models Due to Gas Leak Risk

    Off Grid Trailers is recalling 2021-2022 Expedition, Pando, and Switchback travel trailers because damaged burner control valves may cause a gas leak.

    Product
    OFF GRID TRAILERS — OFF GRID TRAILERS EXPEDITION, SWITCHBACK, PANDO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22C002000·2022-06-07

    Clek Recalls Olli and Ozzi Booster Seats Due to Missing Label

    Clek is recalling Olli and Ozzi booster seats because a required installation diagram is missing, which could lead to improper installation and increased injury risk in a crash.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V397000·2022-06-07

    Kawasaki Recalls LX230 Motorcycles Due to Brake Rotor Defect

    Kawasaki is recalling 2020-2022 LX230 motorcycles because an incorrect front brake rotor may have been installed, reducing brake performance and increasing crash risk.

    Product
    KAWASAKI — KAWASAKI LX230G, LX230A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V401000·2022-06-07

    2021-2022 Mack trucks recalled for defective steering gears

    Mack Trucks is recalling certain 2021-2022 tractor trailers due to steering gears that may fracture, causing loss of steering control and crash risk.

    Product
    MACK — MACK PINNACLE (PI/PN), TE, ANTHEM (AN), GRANITE (GR)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V396000·2022-06-06

    Micro Bird Recalls 2017-2018 G5 School Buses Due to Seat Belt Defect

    Micro Bird is recalling 2017-2018 G5 school buses because an incorrect bracket may interfere with the driver's seat belt pretensioner, increasing injury risk in a crash.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V395000·2022-06-06

    Forest River Recalls 2022 Travel Trailers Due to Table Weld Defect

    Forest River is recalling 2022 East to West Alta and Palomino SolAire travel trailers because incomplete welds on the swing-up table base may cause it to drop unexpectedly, increasing injury risk.

    Product
    EAST TO WEST — EAST TO WEST, PALOMINO ALTA, SOLAIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V394000·2022-06-03

    2023 Freightliner M2 Trucks Steering Shaft Defect Recall

    Daimler Trucks North America is recalling 2023 Freightliner Business Class M2 trucks due to a u-joint pinch bolt that may detach from the steering shaft, causing loss of steering control and increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2, 114SD, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22T009000·2022-06-02

    Goodyear Recalls G159 Tires Due to Tread Separation Risk

    Goodyear is recalling specific G159 tires because the tread may separate, increasing the risk of a crash. Owners should contact dealers for free replacement.

    Product
    TIRES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22147·2022-06-02

    Backcountry Access Tracker4 Avalanche Transceivers Recalled for Toggle Switch Failure

    Backcountry Access Tracker4 Avalanche Transceivers are being recalled because the toggle switch can separate from the unit and prevent it from switching to search mode, which could prevent rescuers from locating a buried skier.

    Product
    Backcountry Access Tracker4 Avalanche Transceivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22146·2022-06-02

    Asweets Recalls Wonder & Wise Baby Activity Walkers for Strangulation Hazard

    Asweets is recalling about 13,300 Wonder & Wise baby activity walkers because rubber rings on the rear wheels can detach, posing a strangulation hazard to young children. No injuries have been reported.

    Product
    Wonder & Wise Baby Activity Walkers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22141·2022-06-02

    Communicorp Recalls Aflac Plush Promotional Ducks for Phthalates and Lead

    Communicorp is recalling about 600,000 six-inch Aflac plush promotional ducks distributed to Aflac employees and customers from February 2009 through March 2021. The ducks contain phthalates and lead levels that exceed federal standards and pose a risk if ingested by young children.

    Product
    6" Aflac Plush Promotional Ducks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22145·2022-06-02

    Children's Robes Recalled Due to Burn Hazard

    Joey Clothing is recalling about 15,930 children's robes sold online because they fail to meet flammability standards for children's sleepwear, posing a risk of burn injuries.

    Product
    Children's robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V393000·2022-06-02

    Winnebago Recalls 2020 ERA Motorhomes Due to Gas Leak Risk

    Winnebago is recalling 2020 ERA motorhomes because damaged burner control valves may cause a gas leak, increasing the risk of fire.

    Product
    WINNEBAGO — WINNEBAGO ERA
    Category
    Vehicle
    Distribution
    Distributed nationwide