The Recall Desk

State

American Samoa product recalls

73,566 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 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

76–100 of 73591

  • SevereNHTSA·26V681000·2026-10-16

    Forest River Recalls 2026-2027 Cedar Creek Trailers for Fire Risk

    Forest River is recalling 2026-2027 Cedar Creek recreational trailers because a slide switch may lack proper overcurrent protection, creating a fire risk.

    Product
    FOREST RIVER — FOREST RIVER CEDAR CREEK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V682000·2026-10-16

    Porsche Recalls 2024 Models for Center Lock Wheel Bolt Fracture Risk

    Porsche is recalling 548 specific 2024 models because a center lock wheel bolt may fracture, causing the wheel to detach and increasing crash risk.

    Product
    PORSCHE — PORSCHE 911, 718 CAYMAN GT4 RS, 911 TURBO S, 911 TURBO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·27024·2026-10-15

    3M Recalls Scotch Thermal Laminators Due to Fire Hazard

    3M is recalling Scotch thermal laminators because they can overheat and catch fire. Consumers should stop using the devices and contact 3M for a refund.

    Product
    Scotch™ Thermal Laminators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·27025·2026-10-15

    HatsanUSA Recalls Blitz Air Rifles Due to Projectile Hazard

    HatsanUSA is recalling Blitz and Blitz 777 air rifles because they can fire unexpectedly, posing a risk of serious injury or death.

    Product
    Blitz and Blitz 777 air rifles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V679000·2026-10-15

    Spartan RV Chassis K2 Recalled for Fuel Hose Separation Risk

    Shyft Group is recalling 2024-2027 Spartan RV Chassis K2 vehicles because remote fuel filter hoses may separate, causing fuel leaks and engine stalls.

    Product
    SPARTAN — SPARTAN RV CHASSIS K2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V677000·2026-10-15

    Volvo Recalls 2025-2026 VNL Trucks for Loose Structural Bolts

    Volvo Trucks North America is recalling 2025-2026 VNL (4) trucks because loose or missing structural bolts in the cab may reduce occupant protection during a crash.

    Product
    VOLVO — 2025 VOLVO VNL (4)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·27028·2026-10-15

    Primark Recalls 101 Dalmatians Coin Purses Due to Phthalate Levels

    Primark is recalling 101 Dalmatians Faux Leather Coin Purses because they contain higher phthalate levels, posing a risk of ingestion by young children.

    Product
    101 Dalmatians Faux Leather Coin Purses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V678000·2026-10-15

    Land Rover Range Rover Recall for Rearview Camera Drainage Issue

    Jaguar Land Rover is recalling 2022-2026 Range Rover vehicles because water may not drain from the rearview camera, potentially causing image failure and increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·27026·2026-10-15

    Loving Thyself Rocks Recalls Crystal Glass Cups Due to Injury Risk

    Loving Thyself Rocks is recalling about 600 crystal glass cups because loose crystal chips can break, posing a risk of serious injury from ingestion and laceration.

    Product
    Crystal Glass Cups with Loose Crystal Chips
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V675000·2026-10-15

    Prevost Buses Recalled for Missing Emergency Exit Instruction Labels

    Prevost is recalling certain buses because the entrance door is missing the emergency exit operating instruction label, which may delay evacuation during an emergency.

    Product
    PREVOST — PREVOST XL-45, XL-40, H3-45, H3-40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0013-2027·2026-10-14

    Berlin Seeds Recalls Alfalfa Sprouting Seeds for Potential E. coli and Salmonella

    Berlin Seeds is recalling alfalfa sprouting seeds due to potential E. coli and/or Salmonella contamination. The product was sold in Ohio and nationwide online.

    Product
    Berlin Seeds Alfalfa Sprouting Seeds, packaged in 1/4 lb., 1/2 lb., 1 lb., and 5 lb. resealable bags and 50 lb. woven poly bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0027-2027·2026-10-14

    Carolina Infusion Recalls Tirzepatide/Cyanocobalamin Injectable Due to Sterility Concerns

    Carolina Infusion, LLC is recalling Tirzepatide/Cyanocobalamin 26/2 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.

    Product
    TIRZEPATIDE/CYANOCOBALAMIN 26/2 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0009-2027·2026-10-14

    K.C. Pharmaceuticals Recalls Leader Ultra Lubricating Eye Drops for Sterility Concerns

    K.C. Pharmaceuticals is recalling 163,008 cartons of Leader Ultra Lubricating Eye Drops due to a lack of assurance of sterility. The product was distributed nationwide under multiple brand names.

    Product
    LEADER ULTRA LUBRICATING EYE DROPS — LEADER ULTRA LUBRICATING EYE DROPS (POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0024-2027·2026-10-14

    FDA Recalls Tri-MIX Injectable Due to Sterility Concerns

    Carolina Infusion, LLC is recalling Tri-MIX injectable syringes because processing equipment used may have compromised the product's sterility.

    Product
    Tri-MIX (PAPAV/PHENTO/ALPROS), 30/1/40, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0026-2027·2026-10-14

    Carolina Infusion Recalls Semaglutide/Cyanocobalamin Injectable Due to Sterility Concerns

    Carolina Infusion, LLC is recalling semaglutide/cyanocobalamin injectable products due to a lack of assurance of sterility related to formulation and processing equipment.

    Product
    SEMAGLUTIDE/CYANOCOBALAMIN 9/2 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0030-2027·2026-10-14

    FDA Recalls Tirzepatide/Cyanocobalamin Injectable Due to Sterility Concerns

    Carolina Infusion, LLC is recalling Tirzepatide/Cyanocobalamin 85/2 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.

    Product
    TIRZEPATIDE/CYANOCOBALAMIN 85/2 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936;
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0006-2027·2026-10-14

    K.C. Pharmaceuticals Recalls Dry Eye Relief Eye Drops for Sterility Concerns

    K.C. Pharmaceuticals is recalling 1,327,248 cartons of dry eye relief eye drops due to a lack of assurance of sterility. The products were distributed nationwide under multiple brand names.

    Product
    LEADER DRY EYE RELIEF EYE DROPS — LEADER DRY EYE RELIEF EYE DROPS (GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0071-2027·2026-10-14

    Steris VERIFY Biological/Integrator Challenge Pack Recall for Spore Population Defect

    Steris is recalling VERIFY Biological/Integrator Challenge Packs because the spore population may be too low, potentially causing false results in steam sterilization monitoring.

    Product
    VERIFY Biological/Integrator Challenge Pack Model/Catalog Number: LCB007
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0036-2027·2026-10-14

    Apothecary Pharma Recalls Tirzepatide Injection Vials Due to Sterility Concerns

    Apothecary Pharma LLC is recalling 22 vials of Tirzepatide Injection due to a lack of assurance of sterility. The affected product was distributed nationwide.

    Product
    Tirzepatide Injection, 18mg/mL, 4 mL Sterile Multi-Dose Vial, Rx only, Apothecary Pharma, LLC, 1913 Evans Road, Cary, NC 27513, NDC 85091-001-18.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0003-2027·2026-10-14

    Good Sense Eye Drops Recalled for Lack of Sterility Assurance

    K.C. Pharmaceuticals is recalling Good Sense Eye Drops Irritation Relief and related brands due to a lack of assurance of sterility.

    Product
    GOODSENSE EYE DROPS IRRITATION RELIEF — GOODSENSE EYE DROPS IRRITATION RELIEF (TETRAHYDROZOLINE HCL, ZINC SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0008-2027·2026-10-14

    K.C. Pharmaceuticals Recalls Multiple Brands of Eye Drops for Sterility Concerns

    K.C. Pharmaceuticals is recalling multiple brands of eye drops, including Leader, Equate, and Walgreens, due to a lack of assurance of sterility.

    Product
    LEADER EYE DROPS REDNESS RELIEF — LEADER EYE DROPS REDNESS RELIEF (GLYCERIN, NAPHAZOLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0086-2027·2026-10-14

    Medline Bariatric Rollator Recalled Due to Front Wheel Detachment Risk

    Medline is recalling 1,824 bariatric rollators because the front wheel assembly may detach, posing a risk of falls and serious injury.

    Product
    Rollator, Bariatric, Basic Steel, Burgundy, mechanical walker with four legs and a metal frame intended for medical purposes to provide moderate weight support while walking, Product Number MDS86800XWS
    Category
    Medical Device
    Distribution
    Distributed nationwide