The Recall Desk

State

American Samoa product recalls

73,190 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 73,190 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15351–15375 of 73215

  • ModerateFDA (Drugs)·D-0886-2023·2023-07-05

    FDA Recalls StellaLife VEGA Oral Care Rinse for Manufacturing Deviations

    The FDA is recalling StellaLife VEGA Oral Care Rinse nationwide due to current Good Manufacturing Practice (cGMP) deviations. The manufacturer voluntarily initiated the recall.

    Product
    STELLALIFE VEGA ORAL CARE RINSE — STELLALIFE VEGA ORAL CARE RINSE (RINSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0881-2023·2023-07-05

    Drug: Arnica 7 Cream Recalled for Manufacturing Standards Deviations

    Homeocare Laboratories is recalling Arnica 7 Cream due to manufacturing standards deviations. The recall affects 2,376 bottles with lot number 2446.

    Product
    Arnica 7 Cream, net wt 2 oz (56.7g), Manufactured for: Brazmedics, LLC, New York, NY 10021 UPC 8 60208 00181 6
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0883-2023·2023-07-05

    Homeopathic diarrhea remedy recalled due to manufacturing control deviations

    Homeocare Laboratories is recalling Babelyn Diarrhea Drops due to manufacturing control (cGMP) deviations. The voluntary recall affects 5,957 bottles distributed nationwide.

    Product
    Babelyn Diarrhea Drops Homeopathic Remedy, 0.5 fl. oz. (15 mL) bottles, Distributed by Pharmadel LLC, Georgetown, DE NDC 55758-035-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0884-2023·2023-07-05

    Drug earache drops recalled due to manufacturing practice deviations

    DoloEar Earache Drops are being recalled due to manufacturing practice deviations. Homeocare Laboratories voluntarily initiated the recall, which was terminated in September 2024.

    Product
    DoloEar Earache Drops, 0.50 fl. oz. bottles, Distributed by Pharmadel LLC, Georgetown, DE NDC 55758-001-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·23V465000·2023-07-03

    Mack LR Garbage Trucks Recalled for Windshield Wiper Defect

    Mack is recalling 2023-2024 LR garbage trucks because loose wiper arm nuts may cause wipers to fail, reducing visibility and increasing crash risk.

    Product
    MACK — MACK LR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V466000·2023-07-03

    Polaris Slingshot Rearview Camera May Freeze, Affecting Visibility

    Polaris is recalling certain Slingshot models because the rearview camera image may freeze or display a blank screen after shifting into reverse. This defect reduces rear visibility and increases the risk of a crash.

    Product
    POLARIS — POLARIS SLINGSHOT S, SLINGSHOT R, SLINGSHOT S TECH, SLINGSHOT SL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·028-2023·2023-06-30

    House of Raeford Recalls Foster Farms Mini Chicken Corn Dogs for Spoilage

    House of Raeford is recalling Foster Farms mini chicken corn dogs due to possible spoilage. No illnesses have been reported.

    Product
    House of Raeford Farms, Inc. — House of Raeford Recalls Foster Farms Brand Mini Chicken Corn Dog Products Due to Possible Spoilage
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·027-2023·2023-06-30

    Panamerican Foods Recalls Ineligible Pork and Beef Bean Stew Products

    Panamerican Foods, LLC is recalling approximately 4,978 pounds of pork and beef bean stew products imported from Brazil. The products were imported from an establishment not eligible to export meat to the U.S.

    Product
    Panamerican Foods, LLC Recalls Ineligible Pork and Beef Bean Stew Products Imported from Brazil
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V463000·2023-06-30

    Mercedes-Benz Recalls C 300 and AMG C43 for Wiring Fire Risk

    Mercedes-Benz is recalling 2022-2023 C 300 and 2023 AMG C43 vehicles because improperly secured electrical wiring ground connections may overheat and cause a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C 300, AMG C43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V462000·2023-06-30

    Mercedes-Benz Recalls C300 and AMG C43 for Wiring Harness Defect

    Mercedes-Benz is recalling 2022-2023 C300 and 2023 AMG C43 vehicles because an incorrectly sized transmission wiring harness may cause damage and loss of drive power.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG C43, C 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V460000·2023-06-30

    Stoughton Recalls 2024 CCGN-40T Trailers Due to Brake Hose Defect

    Stoughton Trailers is recalling 2024 CCGN-40T trailers because brake hoses may be the wrong length or lack fasteners, risking brake failure and crashes.

    Product
    STOUGHTON — STOUGHTON CCGN-40T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V464000·2023-06-30

    Mercedes-Benz Recalls EQS Models for Rear Seat Belt Bolt Issue

    Mercedes-Benz is recalling 2022-2023 EQS 450 and 2022 EQS 580 vehicles because rear seat belt buckle bolts may not be secured properly, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQS 580, EQS 450, EQS450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E049000·2023-06-30

    Maxzone Recalls DEPO Rear Turn Signal Lights for Size Non-Compliance

    Maxzone is recalling specific DEPO rear turn signal lights that may be smaller than federal safety standards require, potentially reducing visibility to other drivers.

    Product
    EXTERIOR LIGHTING:TURN SIGNAL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·23237·2023-06-29

    CaTeam Canvas Baby Hammock Swings Recalled for Suffocation Hazard

    CaTeam is recalling about 700 Canvas Baby Hammock Swings sold online from November 2022 through January 2023 because they violate the Safe Sleep for Babies Act. The inclined design poses a suffocation risk to infants.

    Product
    Canvas Baby Hammock Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23234·2023-06-29

    Bose Acoustimass, Lifestyle, and Companion Bass Modules Due to Fire Hazard

    Bose Corporation is recalling select bass modules manufactured before April 2006 because electrical components can fail and cause fires. The firm has received 21 reports of ignition or melting worldwide, with three resulting in property damage.

    Product
    Bose Acoustimass, Lifestyle and Companion bass modules (produced before April 2006)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V458000·2023-06-29

    2020–2023 Honda Ridgeline Brake Master Cylinder Separation Recall

    Honda is recalling certain 2020–2023 Ridgeline vehicles because a fastener connecting the brake booster and master cylinder may have been improperly assembled, risking brake failure and crashes.

    Product
    HONDA — HONDA, ACURA PASSPORT, RIDGELINE, PILOT, CIVIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V457000·2023-06-29

    Hino Recalls 2023 NE7A, NV7A, and NJ7A Trucks for Front Axle Defect

    Hino is recalling 2023 NE7A, NV7A, and NJ7A trucks because over-tightened front axle U-bolts may break, potentially causing loss of vehicle control.

    Product
    HINO — HINO NE7A, NV7A, NJ7A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V455000·2023-06-29

    2023 Grand Design travel trailers recalled for improperly tightened axle fittings

    Grand Design is recalling certain 2023 Momentum and Reflection travel trailers with 5200 and 6000 CURT RV axles due to improperly tightened grease fittings that may separate, risking wheel detachment and crashes.

    Product
    GRAND DESIGN — GRAND DESIGN MOMENTUM, REFLECTION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23235·2023-06-29

    Victrola Wood Metropolitan Bluetooth Record Players Recalled for Fire Hazard

    Victrola is recalling about 5,700 Wood Metropolitan Bluetooth Record Players because they can overheat and catch fire. The company has received six reports of overheating or fire, including one minor injury and one report of minor property damage.

    Product
    Wood Metropolitan Bluetooth Record Players with 3-Speed Turntables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23771·2023-06-29

    H-E-B Leather Woven Chairs Recalled for Fall Hazard

    H-E-B is recalling about 1,400 Haven & Key Leather Woven Chairs because the backrest and legs can crack and break off when someone is seated, creating a fall hazard. The firm has received 11 reports of cracking or breaking, with no injuries reported.

    Product
    Haven & Key Leather Woven Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1742-2023·2023-06-28

    Medtronic CRT-D Defibrillators: Rare Energy Output Failure Risk During Therapy

    Medtronic implantable cardioverter defibrillators (CRT-D) may deliver reduced or no energy during high-voltage therapy due to manufacturing defect in the feedthrough component. FDA Class I recall affects 182 units.

    Product
    CRT-D DTBB1D4 VIVA S IS1/DF4 US, Model Number DTBB1D4; Implantable Cardioverter Defibrillators
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1725-2023·2023-06-28

    Medtronic Implantable Cardioverter Defibrillators Recalled for Potential Therapy Failure

    Medtronic's ICD COBALT defibrillators may fail to deliver critical therapy due to a manufacturing defect in a power delivery component. Patients should contact their physician to determine if affected.

    Product
    ICD COBALT DR MRI IS1 DF1, Model Number DDPB3D1; Implantable Cardioverter Defibrillators
    Category
    Medical Device
    Distribution
    Distributed nationwide