The Recall Desk

State

American Samoa product recalls

73,376 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 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19976–20000 of 73401

  • SevereNHTSA·22V467000·2022-07-01

    Mercedes-Benz Recalls 2022 EQS Models for Bumper Tow Ring Defect

    Mercedes-Benz is recalling 2022 EQS 450, EQS 580, and AMG EQS 53 vehicles because the bumper tow ring assembly may detach, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQS 580, EQS 450, AMG EQS 53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V474000·2022-07-01

    2022 Oliver Legacy Elite II Travel Trailer Bearing Washer Recall

    The 2022 Oliver Travel Trailers Legacy Elite II may have a cracked bearing washer in the hub assembly that could cause the hub to separate from the axle, risking loss of vehicle control. Owners should contact Oliver at 1-866-205-2621 for a free replacement.

    Product
    OLIVER TRAVEL TRAILERS — OLIVER TRAVEL TRAILERS LEGACY ELITE II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V473000·2022-07-01

    2022 Subaru Outback Engine Wiring Harness Damage Causes Stall Risk

    The engine wiring harness may be damaged in 2022 Subaru Outback vehicles, causing a loose connection to the engine control unit. This could cause engine stalls and increase crash risk.

    Product
    SUBARU — SUBARU OUTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22177·2022-06-30

    Children's Pajamas Recalled for Flammability Standards Violation

    Kids Tales-branded children's pajamas fail to meet federal flammability standards for sleepwear, posing a burn injury risk. About 9,100 units sold online at Amazon from November 2021 through April 2022 are affected.

    Product
    Children's Pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V468000·2022-06-30

    Freightliner recalls 2022 Cascadia trucks for parking brake failure

    Daimler Trucks is recalling certain 2022 Freightliner Cascadia trucks because the electronic parking brake may fail to engage when turned off, risking vehicle rollaway. Owners should contact dealers for free repair.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22175·2022-06-30

    RIO-Branded Swinging Hammock Chairs Recalled Due to Collapse Injury Hazard

    ShelterLogic Group is recalling approximately 786,000 RIO-branded swinging hammock chairs because improper pin insertion during assembly can cause the chair's legs to collapse, injuring users. The company has received 24 reports of injuries including bruises, lacerations, concussions, and back strain.

    Product
    RIO-branded Swinging Hammock Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22754·2022-06-30

    Mohnark Lidocaine 4% Topical Anesthetic Cream Recalled for Non-Child-Resistant Packaging

    Mohnark Pharmaceuticals is recalling Lidocaine 4% Topical Anesthetic Cream because the packaging does not meet child-resistant requirements, creating a poisoning risk if young children ingest the product. About 9,000 units sold online were affected.

    Product
    Lidocaine 4% Topical Anesthetic Cream
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·22176·2022-06-30

    Laars Residential Gas-Fired Boilers Recalled for Carbon Monoxide Risk

    Laars Heating Systems is recalling about 545 residential gas-fired boilers because a malfunctioning blocked vent temperature switch can release carbon monoxide into homes. No injuries have been reported.

    Product
    Residential atmospheric gas-fired boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V465000·2022-06-30

    GM Recalls 2018-2020 Buick Regal for Brake Software Error

    General Motors is recalling 2018-2020 Buick Regal vehicles because a software error may cause loss of power brake assist, increasing stopping distance.

    Product
    BUICK — BUICK REGAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22178·2022-06-30

    Children's Nightgowns Recalled for Flammability Standards Violation

    iMOONZZZ children's nightgowns sold on Amazon fail to meet federal flammability standards for sleepwear, posing a burn injury risk. About 2,000 units sold between June 2019 and May 2022 are affected.

    Product
    Children's Nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V463000·2022-06-30

    2022 Chevrolet Silverado 1500 accessory brake light may not function properly

    General Motors is recalling certain 2022 Chevrolet Silverado and GMC Sierra trucks with an accessory sport bar. The high-mounted brake light may not function or may be blocked, reducing visibility to other drivers and increasing crash risk.

    Product
    GMC — GMC, CHEVROLET SIERRA 1500, SILVERADO 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·22753·2022-06-30

    Yamaha Kodiak 700 ATVs Recalled for Missing Load Limit Label

    Yamaha is recalling about 3,500 Model Year 2021 and 2022 Kodiak 700 ATVs because they are missing the "Maximum Loading Limit" label, which can result in unsafe trailer towing and crash hazards.

    Product
    Model Year 2021 and 2022 Kodiak 700 All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1339-2022·2022-06-29

    Peanut Butter Fudge Recalled Due to Potential Salmonella Contamination

    Calico Cottage Inc is recalling Peanuttiest Caramel Chocolate fudge nationwide because the peanut butter ingredient may be contaminated with Salmonella.

    Product
    1. PEANUTTIEST CARAMEL CHOCOLATE P-MADE(6SS)6LB NT WT - not consumer packaging, bulk carton
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1338-2022·2022-06-29

    Peanut Butter Fudge Recalled for Potential Salmonella Contamination

    Calico Cottage Inc is recalling peanut butter fudge products due to potential Salmonella contamination in the peanut butter ingredient. The recall affects bulk carton products distributed nationwide.

    Product
    1. PEANUT BUTTER FUDGE (3 - 6LB SLABS/CS) 18LB NET WT - not consumer packaging, bulk carton 2. PEANUT BUTTER FUDGE (6S) 6LB NET WT- not consumer packaging, bulk carton 3. PEANUT BUTTER FUDGE (6SS) 6LB NET WT- not consumer packaging, bulk carton
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1271-2022·2022-06-29

    Medfusion Syringe Pump Recalled Due to Multiple Infusion Control and Alarm Failures

    Smiths Medical recalled 58,671 Medfusion Syringe Pump units worldwide due to multiple failures that could interrupt therapy or cause over-infusion, including defective alarms and display errors.

    Product
    Medfusion Syringe Pump Model: Model 4000-0100-50, Model 4000-0101-249, Model 4000-0101-50, Model 4000-0101-51, Model 4000-0101-78, Model 4000-0105-249, Model 4000-0105-51, Model 4000-0105-78, Model 4000-0106-00, Model 4000-0106-01, Model 4000-0106-231
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1321-2022·2022-06-29

    Chocolate Peanut Butter Cups Recalled for Salmonella Contamination

    Albanese Confectionery Group recalls Rich's Milk Chocolate peanut butter cups nationwide due to Salmonella contamination from recalled Jif peanut butter used in manufacturing.

    Product
    Rich s Milk Chocolate Giant Layered Peanut Butter and Cups Rich s Milk Chocolate Mini Peanut Butter Cups; 2ct 5lb bulk per 10 lb case. Product not retail packaged, distributed for bulk sale at retail.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1337-2022·2022-06-29

    Chocolate fudge with peanut butter recalled for potential Salmonella

    Calico Cottage Inc is recalling chocolate fudge products containing peanut butter due to potential Salmonella contamination. The recall affects 677 units distributed nationwide.

    Product
    1. PEANUT BUTTER CHOC (3 - 6LB SLABS/CS) 18LB NET WT - Not consumer packaging, bulk carton 2. PEANUT BUTTER CHOC FUDGE LAYERED (6S) 6LB NET WT - not consumer packaging, bulk carton 3. PEANUT BUTTER CHOCOLATE FUDGE (6SS) 6LB NET WT - not consumer packaging, bulk carton
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1272-2022·2022-06-29

    Medfusion Syringe Pump Class I Recall: Risk of Over-Infusion or Therapy Interruption

    Smiths Medical is recalling multiple Medfusion Syringe Pump models due to software and hardware defects that may interrupt drug infusion or cause over-infusion. Approximately 65,093 units distributed worldwide are affected.

    Product
    Medfusion Syringe Pump Models: 3500, 3500-0600-00, 3500-0600-01, 3500-0600-249, 3500-0600-50, 3500-0600-51, 3500-0600-82, 3500-306, 3500-402, 3500-414, 3500-415, 3500-500, 3500BC, 3500E, 3500G, 3500SD, 3500SD-500, 3500VX, 3500VX-306, 3500VX-414, 3500VX-415, 3500VX-500, 3500ZE…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1266-2022·2022-06-29

    HeartWare HVAD Battery Model 1650DE May Malfunction Due to Weld Defect

    Medtronic is recalling HeartWare HVAD batteries (Model 1650DE) due to an internal weld defect that can cause battery malfunction and prevent proper charging. Approximately 429 affected batteries were distributed worldwide.

    Product
    HeartWare Battery, Model #1650DE, a component of the HeartWare Ventricular Assist Device (HVAD) System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1340-2022·2022-06-29

    Salted Nut Roll Fudge Recalled for Potential Salmonella in Peanut Butter

    Calico Cottage Inc is recalling Salted Nut Roll Pre-Made Fudge nationwide because the peanut butter ingredient is potentially contaminated with Salmonella.

    Product
    1. SALTED NUT ROLL PRE-MADE FUDGE (6SS) 6LB NET WT - not consumer package, bulk carton
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1274-2022·2022-06-29

    Colonovideoscope Model CF-H180AL recalled due to narrowed viewing angle

    Olympus Corporation recalls a single colonovideoscope model CF-H180AL because an incorrect camera unit was installed, causing narrower viewing angle and potential device protrusion that could injure tissue. No injuries have been reported.

    Product
    Colonovideoscope Model CF-H180AL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1156-2022·2022-06-29

    Tretinoin Capsules Recalled Nationwide for Failed Dissolution Specifications

    Teva Pharmaceuticals is recalling Tretinoin Capsules (10 mg) nationwide due to failed dissolution specifications that may affect medication effectiveness. Patients should contact their pharmacist or doctor to confirm if their prescription is affected.

    Product
    Tretinoin Capsules, 10 mg, Rx Only, 100 capsules per bottle, Teva Pharmaceuticals USA Inc., North Wales, PA, 19454, NDC 0555-0808-02.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1153-2022·2022-06-29

    Testosterone Cypionate Injectable Recalled for Manufacturing Quality Issues

    Sun Pharmaceutical recalls 97,450 vials of Testosterone Cypionate Injection nationwide due to manufacturing deviations that could cause out-of-specification impurities.

    Product
    TESTOSTERONE CYPIONATE — TESTOSTERONE CYPIONATE (TESTOSTERONE CYPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1154-2022·2022-06-29

    Testosterone Cypionate Injectable Recalled Due to Manufacturing Sterility Deviation

    Sun Pharmaceutical is recalling approximately 47,500 vials of Testosterone Cypionate Injection due to a manufacturing deviation that may have affected product sterility.

    Product
    TESTOSTERONE CYPIONATE — TESTOSTERONE CYPIONATE (TESTOSTERONE CYPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide