The Recall Desk

State

American Samoa product recalls

73,096 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 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

11001–11025 of 73121

  • HighCPSC·24257·2024-06-06

    FURminator deShedding Dog Conditioner Recalled for Bacterial Contamination

    Spectrum Brands is recalling about 102,000 units of FURminator deShedding Ultra Premium Dog Conditioner (1 Gallon) because the product can contain Pseudomonas aeruginosa bacteria, which poses a serious infection risk to people with weakened immune systems or external medical devices.

    Product
    FURminator deShedding Ultra Premium Dog Conditioner (1 Gallon)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24255·2024-06-06

    Biometric Firearm Safes Recalled for Unauthorized Access Risk

    SA Consumer Products is recalling Sanctuary Quick Access and Sports Afield Biometric Firearm Safes because the biometric lock can be opened by unauthorized users, posing a serious injury hazard and risk of death. No injuries have been reported.

    Product
    Sanctuary and Sports Afield Biometric Firearm Safes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24258·2024-06-06

    Sling Carriers Recalled for Infant Suffocation and Fall Hazards

    About 1,160 sling carriers sold on Walmart.com through Joybuy Marketplace Express are recalled due to violations of federal safety standards. The carriers pose suffocation and fall hazards to infants because they lack required structural integrity, occupant retention, and proper restraint systems.

    Product
    Sling Carriers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V415000·2024-06-06

    2022 RAM 2500 Electronic Stability Control Software Defect

    Chrysler is recalling 2022 RAM 2500 and 3500 vehicles due to an ABS control module software malfunction that can disable the electronic stability control system, increasing crash risk. Dealers will provide a free software update.

    Product
    RAM — RAM, DODGE 2500, DURANGO, 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24E047000·2024-06-06

    Chrysler Recalls MOPAR ABS Control Modules for Software Malfunction

    Chrysler is recalling MOPAR anti-lock braking system control modules used as replacement parts in 2022 Dodge Durango and Ram 2500/3500 vehicles. A software malfunction may disable electronic stability control, increasing crash risk.

    Product
    SERVICE BRAKES, AIR:ANTILOCK:CONTROL UNIT/MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V416000·2024-06-06

    RAM ProMaster vehicles recalled for missing side door beam and incorrect seating label

    Certain 2021-2024 RAM ProMaster vehicles lack a side door beam and have incorrect seating capacity information on the tire placard. These defects may reduce occupant protection in side-impact crashes and could result in improper vehicle loading.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V414000·2024-06-06

    2024 Jeep Wrangler Recalled for Trailer Lighting Malfunction

    Chrysler is recalling 2024 Jeep Wrangler vehicles because the power distribution center may prevent trailer turn signals and taillights from operating, increasing crash risk.

    Product
    JEEP — JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·24259·2024-06-06

    Wild Country Ropeman 1 Ascenders Recalled for Failure to Engage

    Salewa USA recalls Wild Country Ropeman 1 ascenders because the teeth can fail to engage, making it difficult or impossible to ascend. About 7,700 units sold in the United States since December 2022.

    Product
    Wild Country Ropeman 1 ascenders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V407000·2024-06-05

    2023 Kia Telluride power seat motor fire risk recall

    Kia is recalling certain 2023 Telluride vehicles due to a fire risk in the front power seat motor caused by a stuck seat slide knob. Owners should park outside until repairs are completed.

    Product
    KIA — KIA TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0511-2024·2024-06-05

    Compounded Tirzepatide Vials Mislabeled with Testosterone Cypionate

    Revive Rx Pharmacy recalls 751 vials of compounded tirzepatide (Lot #748127) labeled to contain tirzepatide but actually filled with testosterone cypionate. Patients receiving this medication may take the wrong drug with serious health consequences.

    Product
    Tirzepatide 10 mg/0.5 mL Sterile Solution, 2 mL Multi-dose vial, Rx only, This is a Compounded Product By: Revive RX Pharmacy, 3831 Golf Dr A, Houston, TX 77018, internally assigned NDC 99000-9278-64
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1876-2024·2024-06-05

    Medline Sub-G Endotracheal Tubes with Subglottic Suctioning—Inflation and Suction Defects

    Medline endotracheal tubes with subglottic suctioning may have inflation tubes that detach or tear and suction pumps that disconnect, risking loss of ventilation control.

    Product
    Medline Sub-G Endotracheal Tube with Subglottic Suctioning: (1) REF DYNJ18860, Polyurethane Cuff 6.0 mm ID; (2) REF DYNJ18865, Polyurethane Cuff 6.5 mm ID; (3) REF DYNJ18870, Polyurethane Cuff 7.0 mm ID; (4) REF DYNJ18875, Polyurethane Cuff 7.5 mm ID; (5) REF DYNJ18880, Po
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V408000·2024-06-05

    Rivian R1S and R1T damaged pillar clips affect airbag deployment

    Rivian is recalling certain 2022-2024 R1S and R1T vehicles. Damaged attachment clips on pillar trim panels may prevent proper side curtain airbag deployment in a crash, increasing injury risk.

    Product
    RIVIAN — RIVIAN R1T, R1S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V411000·2024-06-05

    Vermeer Recalls 2023 Vacuum Excavator Trailers Due to Frame Defect

    Vermeer is recalling 2023 LPSDT vacuum excavator trailers because the frame may bend or distort, potentially causing loss of stability and control while towing.

    Product
    VERMEER — VERMEER VACUUM EXCAVATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V412000·2024-06-05

    2024 Hyundai Tucson and Santa Cruz power steering defect recall

    Hyundai is recalling 2024 Tucson and Santa Cruz vehicles due to a potential circuit board short in the power steering system. Loss of steering assist could increase crash risk.

    Product
    HYUNDAI — HYUNDAI TUCSON, SANTA CRUZ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1271-2024·2024-06-05

    Mother's Day Heart Box Recalled for Undeclared Coconut Allergen

    Maribel's Sweets, Inc. is recalling its 7.7-piece Mother's Day heart box due to undeclared coconut. The product may pose a risk to consumers with coconut allergies. Approximately 4,011 boxes were distributed nationwide and through online retailers.

    Product
    7. 7pc Mother s Day heart box
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1265-2024·2024-06-05

    Ganache tote boxes recalled for undeclared coconut allergen

    Maribel's Sweets, Inc. is recalling 4,011 ganache tote boxes containing undeclared coconut. The product was distributed nationwide through e-commerce and retail stores in New York.

    Product
    1. 2pc Ganache tote box
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1273-2024·2024-06-05

    Mother's Day Heart Ganache Boxes Recalled for Undeclared Coconut

    Maribel's Sweets, Inc. is recalling Mother's Day heart ganache boxes because they contain undeclared coconut, an allergen not listed on the label. This poses a risk to consumers with tree nut allergies.

    Product
    9. 25pc Mother s Day heart ganache box
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1900-2024·2024-06-05

    EsophaCap Sponge May Detach From String During Removal

    Lucid Diagnostics is recalling EsophaCap medical devices (220 units in MN and MD) because the sponge may detach from the string during removal, particularly at esophageal sphincters.

    Product
    Brand Name: EsophaCap Product Name: EsophaCap (25mm diameter, 10 pores/inch) Model/Catalog Number: EC25T10VI Software Version: N/A Product Description: EsophaCap is pouched as individual units. 10 units go into a shelf-box. Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V405000·2024-06-05

    2023 Fisker Ocean Recall: Instrument Cluster Warning Lights Display Incorrectly

    Fisker is recalling 2023 Ocean vehicles because warning lights display with incorrect font sizes and colors, and fail to illuminate during bulb checks. The defect risks drivers missing critical safety information.

    Product
    FISKER — FISKER OCEAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V403000·2024-06-05

    Timpte Recalls 2024-2025 Deck Trailers Due to Ramp Bolt Defect

    Timpte is recalling 2024-2025 1420 and 1424 deck trailers because retaining rod bolts may fall off, leaving the folding ramp unsecured and increasing injury risk.

    Product
    TIMPTE — TIMPTE TIMPTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0517-2024·2024-06-05

    Metoprolol Tartrate Tablets Recalled Nationwide for Metal Contamination

    Rubicon Research is recalling 11,664 bottles of Metoprolol Tartrate 25mg tablets nationwide due to the presence of metal in the tablets. Consumers should discontinue use and contact their healthcare provider.

    Product
    METOPROLOL TARTRATE — METOPROLOL TARTRATE (METOPROLOL TARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·24V404000·2024-06-05

    2023 Fisker Ocean Software Defect Causes Loss of Drive Power

    Fisker is recalling all 2023 Ocean vehicles. A software defect in the MCU/VCU can cause unexpected loss of drive power, increasing crash risk.

    Product
    FISKER — FISKER OCEAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1268-2024·2024-06-05

    Maribel's Sweets 6-piece ganache boxes recalled for undeclared coconut

    Maribel's Sweets, Inc. is recalling 4,011 boxes of 6-piece signature ganache chocolate boxes due to undeclared coconut. Consumers with coconut allergies are at risk.

    Product
    4. 6pc signature ganache box
    Category
    Food
    Distribution
    Distributed nationwide