The Recall Desk

State

American Samoa product recalls

73,100 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 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12026–12050 of 73125

  • HighCPSC·24172·2024-03-21

    BRS and BULin Liquid Fuel Bottles Recalled for Unsafe Closures

    BRS and BULin portable liquid fuel bottles sold on Amazon have non-child-resistant closures that violate federal safety law, posing risks of burns and poisoning to children. Consumers should stop using them and contact the seller for disposal and refund instructions.

    Product
    BRS and BULin Liquid Fuel Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24167·2024-03-21

    Fisher-Price Little People figures recalled due to detachable head choking hazard

    Fisher-Price is recalling Mickey and Friends figures sold since May 2023 because Donald and Daisy Duck heads can detach, posing a choking hazard. Three detachments were reported, including one found in a child's mouth, with no injuries.

    Product
    Fisher-Price Little People Mickey and Friends Figures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V217000·2024-03-20

    Porsche Taycan high voltage batteries may short circuit within modules

    Porsche is recalling certain 2020-2024 Taycan vehicles because the high-voltage battery may experience a short circuit within the battery modules, increasing the risk of fire.

    Product
    PORSCHE — PORSCHE TAYCAN, TAYCAN 4S, TAYCAN GTS, TAYCAN TURBO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V215000·2024-03-20

    Additional Porsche Taycan models recalled for high voltage battery short circuits

    A second Porsche recall covers certain 2020-2023 Taycan vehicles because the high-voltage battery may experience a short circuit within the battery modules. 606 units affected.

    Product
    PORSCHE — PORSCHE TAYCAN 4S, TAYCAN GTS, TAYCAN TURBO, TAYCAN 4 CROSS TURISMO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V213000·2024-03-20

    Prevost coach coolant heaters may overheat and emit excessive exhaust gas

    Prevost is recalling certain H3-45, H3-45 VIP and X3-45 coaches because the coolant heaters may generate excessive exhaust gas and overheat. 37 units are affected.

    Product
    PREVOST — PREVOST H3-45 VIP, H3-45, X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V216000·2024-03-20

    LiveWire rear axle and shock joint nuts may not be tightened

    LiveWire is recalling certain 2024 S2 Del Mar motorcycles because the rear axle and lower shock joint nuts may not have been properly tightened. 165 units are affected.

    Product
    LIVEWIRE — LIVEWIRE S2 DEL MAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1071-2024·2024-03-20

    Trader Joe's Southwest Salad Recalled Due to Listeria Monocytogenes Contamination

    Trader Joe's Company is recalling Trader Joe's Southwest Salad (SKU 56077), 9 oz. due to potential Listeria monocytogenes contamination. Approximately 800,955 units were distributed nationwide.

    Product
    Trader Joe s Southwest Salad (SKU 56077) 9 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V214000·2024-03-20

    Kia Telluride driveshafts may not fully engage, allowing roll away

    Kia is recalling certain 2020-2024 Telluride vehicles because the intermediate shaft and right front driveshaft may not be fully engaged, which can result in roll away while in PARK.

    Product
    KIA — KIA TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1069-2024·2024-03-20

    Trader Joe's Cilantro Salad Dressing Recalled for Listeria Contamination

    Trader Joe's is recalling Cilantro Salad Dressing (SKU 36420) due to possible Listeria monocytogenes contamination. Approximately 15,890 cases were distributed nationwide.

    Product
    Trader Joe s Cilantro Salad Dressing (SKU 36420) Perishable Keep Refrigerated 12 FL OZ (355mL)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1070-2024·2024-03-20

    Trader Joe's Elote Chopped Salad Kit Recalled for Listeria Contamination

    Trader Joe's Company is recalling approximately 7,348 cases of Trader Joe's Elote Chopped Salad Kit nationwide due to potential Listeria monocytogenes contamination. All products with "Used By" dates on or before February 18, 2024 are affected.

    Product
    Trader Joe s Elote Chopped Salad Kit (SKU 74768) 11.94 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1293-2024·2024-03-20

    EasyPoint Needle may detach inside patient during use

    Retractable Technologies is recalling EasyPoint Needles (25G x 5/8", REF: 82091) because the needle cannula may detach from the needle holder inside the patient.

    Product
    EasyPoint Needle, 25G x 5/8", REF: 82091
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0376-2024·2024-03-20

    TRP Blur Relief Eye Drops Recalled Nationwide for Sterility Assurance Failure

    TRP Blur Relief sterile eye drops (Lot #B905) are recalled due to inability to assure product sterility. Approximately 7,248 bottles were distributed nationwide.

    Product
    TRP Blur Relief, Sterile Eye Drops, Homeopathic 0.5 FL OZ (15mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-002-11.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0374-2024·2024-03-20

    FDA Recalls Betimol Eye Drops for Sterility and Container Closure Defects

    Thea Pharma is recalling Betimol (timolol) ophthalmic solution nationwide for lack of sterility assurance and compromised container closure. The defects could allow contamination of the eye medication.

    Product
    BETIMOL — BETIMOL (TIMOLOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0380-2024·2024-03-20

    TRP Natural Eyes Floaters Relief eye drops recalled due to sterility concerns

    Optikem International is recalling TRP Natural Eyes Floaters Relief eye drops nationwide due to lack of assurance of sterility in manufacturing. Affected bottles have lot numbers F404, F405, or F406.

    Product
    TRP Natural Eyes Floaters Relief, Sterile Eye Drops, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-098-15.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0375-2024·2024-03-20

    TRP Natural Eyes Allergy Relief Eye Drops Recalled for Sterility Assurance Issues

    Optikem International is recalling TRP Natural Eyes Allergy Eyes Relief eye drops due to lack of assurance of sterility. The recall affects 30,240 bottles distributed nationwide.

    Product
    TRP Natural Eyes Allergy Eyes Relief, Sterile Eye Drops, Homeopathic 0.33 FL OZ (10mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-032-15.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0381-2024·2024-03-20

    TRP Natural Eyes eye drops recalled due to lack of sterility assurance

    TRP Natural Eyes Aging Eye Relief eye drops are being recalled because the manufacturer cannot assure the product meets sterility requirements. The recall affects 19,344 bottles distributed nationwide.

    Product
    TRP Natural Eyes Aging Eye Relief, Sterile Eye Drops, Homeopathic, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-027-15.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0379-2024·2024-03-20

    TRP Eye Strain Relief Eye Drops Recalled Due to Lack of Sterility Assurance

    Optikem International recalls TRP Eye Strain Relief eye drops nationwide due to lack of assurance of sterility. Affected units are 10 mL bottles with Lot E206.

    Product
    TRP Eye strain Relief, Sterile Eye Drops, Homeopathic, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-172-15.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1292-2024·2024-03-20

    Shimadzu Trinias Digital Angiography System Recalled for Capacitor Defect

    Shimadzu has recalled the Trinias Digital Angiography System due to a capacitor manufacturing issue that could cause abnormal display or system malfunction. No injuries have been reported.

    Product
    Shimadzu, Trinias, Digital Angiography System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1054-2024·2024-03-20

    Coffee recalled for potential allergen contact with almonds, pecans, coconut

    House of Coffee Beans, Inc is recalling coffee products distributed in Texas, South Carolina, and North Carolina due to potential cross-contact with almonds, pecans, and coconut. Consumers with allergies to these ingredients should not consume affected products.

    Product
    Coffee 5 pound bags, 2 pound bags, 1 pound bags, 12 ounce bags, half pound bags and/or 6 ounce bags
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1299-2024·2024-03-20

    SPII Lubinus Hip Prosthesis Recalled Due to Carton Label Interpretation Guidance

    Waldemar Link is recalling SPII Model Lubinus Long Stem Prosthesis XL Neck implants due to carton labeling that could be misinterpreted during surgery. Clearer guidance is being provided to prevent surgical misapplication.

    Product
    SPII Model Lubinus, Long Stem Prosthesis XL Neck, cemented
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0385-2024·2024-03-20

    Antibiotic Injection Recalled for Failed Stability Specification

    Eugia US LLC is recalling 1,160 vials of Tobramycin for Injection due to failed water determination testing. Affected lot numbers are 3TB23001 and 3TB23002, expiring 04/30/2025.

    Product
    TOBRAMYCIN — TOBRAMYCIN (TOBRAMYCIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1278-2024·2024-03-20

    D-Clip Applier Recalled for Failure to Release During Surgery

    Peter Lazic GmbH's D-Clip Standard/Mini Applier is being recalled after a customer complaint that the device failed to release the clip during surgery, with the applier remaining attached to the clip.

    Product
    D-Clip Standard/Mini Applier, 210mm bayonet, jaw rigid, double action.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1290-2024·2024-03-20

    CARTO VIZIGO Guiding Sheath Recalled for Manufacturing Validation Issue

    Biosense Webster is recalling CARTO VIZIGO Bi-Directional Guiding Sheaths after inadvertently mixing unvalidated devices into production. The recall affects 853 units distributed nationwide.

    Product
    CARTO VIZIGO Bi-Directional Guiding Sheath, REF D128502 The CARTO VIZIGOTM Bi-Directional Guiding Sheath is designed to provide accessibility and maneuverability in the cardiac anatomy. The steerable sheath is fitted with a hemostasis valve to minimize blood loss during…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0370-2024·2024-03-20

    Potassium Chloride Injection Recalled Due to Pinhole Container Defects

    B. Braun Medical is recalling 22,752 bags of Potassium Chloride for Injection Concentrate nationwide due to pinholes in container bags that compromise sterility assurance. Affected lots are J2S007 (expires 12/31/2024) and J3A115 (expires 01/31/2025).

    Product
    POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide