The Recall Desk

State

American Samoa product recalls

73,213 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 73,213 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

16576–16600 of 73238

  • ModerateFDA (Drugs)·D-0478-2023·2023-04-05

    Prescription Drug Ropinirole 0.25 mg Tablets Recalled for Manufacturing Deviations

    Direct Rx is recalling Ropinirole, USP, 0.25 mg tablets (NDC 72189-0364-30, Lot 21JU2210) nationwide due to Good Manufacturing Practice (cGMP) deviations. The firm voluntarily initiated this recall on March 13, 2023.

    Product
    Ropinirole, USP, 0.25 mg Tablets, Rx Only, Packaged as a 30-count bottle, NDC 72189-0364-30; Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0480-2023·2023-04-05

    Drug Recall: Glimepiride Tablets Due to Manufacturing Deviations

    Direct Rx is recalling Glimepiride, USP, 1 mg Tablets nationwide due to cGMP deviations. The firm-initiated recall impacts both 30-count and 90-count bottles distributed across the USA.

    Product
    Glimepiride, USP, 1 mg Tablets, Rx Only, Packaged as a a) 30-count bottle, NDC 61919-0723-30; b) 90-count bottle, NDC 61919-0723-90 Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0485-2023·2023-04-05

    Simvastatin 20mg Tablets Recalled for Manufacturing Practice Deviations

    Direct Rx recalled Simvastatin 20mg tablets nationwide due to manufacturing practice deviations. The voluntary recall affects bottles distributed across the United States.

    Product
    Simvastatin, USP, 20 mg Tablets, Rx Only, Packaged as a a) 30-count bottle, NDC 61919-0446-30 b) 90-count bottle, NDC 61919-0446-90, Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1301-2023·2023-04-05

    PCRopsis Support Medical Device Recall Due to Misleading Label Statements

    Entopsis, Inc. is recalling PCRopsis Support nucleic acid extraction reagents due to misleading statements on product labels. No illnesses or injuries have been reported.

    Product
    PCRopsis Support: a) 1 mL, REF 787001; b) 0.25 mL, REF 787002; c) 25 uL, REF 787003; Improves the functionality of PCRopsis regents for select applications; nucleic acid extraction from a variety of biological samples
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0483-2023·2023-04-05

    Drug Recall: Simvastatin 5 mg tablets due to manufacturing compliance violations

    Direct Rx is recalling 51 bottles of Simvastatin 5 mg tablets nationwide due to Good Manufacturing Practice deviations. The recall is voluntary and was initiated in March 2023.

    Product
    Simvastatin, USP, 5 mg Tablets, Rx Only, Packaged as a 90-count bottle, NDC 61919-0710-90 Packaged and Distributed By: Direct Rx, Dawsonville, GA 30534
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0477-2023·2023-04-05

    Finasteride Tablets Recalled Nationwide for Manufacturing Practice Deviations

    Direct Rx is recalling 19 bottles of Finasteride 5 mg Tablets nationwide due to cGMP deviations. The firm initiated this recall voluntarily.

    Product
    Finasteride, USP, 5 mg Tablets, Rx Only, Packaged as a 90-count bottle, NDC 61919-0733-90; Packaged and Distributed By: Direct Rx
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1298-2023·2023-04-05

    Medical device lysis beads recalled for misleading label statements

    Entopsis recalls PCRopsis Lysis Beads (363 units) due to misleading label statements on the product packaging. The affected product was distributed nationwide and to Canada, UK, Portugal, Spain, Germany, Brazil, Denmark, South Korea, Colombia, and Lithuania.

    Product
    PCRopsis Lysis Beads, IVDD: a) 25 tubes , REF 597000; b) 25 tubes, REF 597825; c) 50 tubes, REF 597850; d) 25 grams, REF 5970025; e) 1000 kilogram, REF 5971000; coated beads that facilitate lysis of microorganisms; nucleic acid extraction from a variety of biological samples
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1305-2023·2023-04-05

    ACL ELITE PRO-Analyzer: HemosIL Liquid Anti-Xa test definition removed

    Instrumentation Laboratory is removing the HemosIL Liquid Anti-Xa test definition from ACL ELITE/Elite Pro analyzers used in clinical hemostasis laboratories. No illnesses or injuries have been reported.

    Product
    ACL ELITE PRO-Analyzer designed specifically for clinical use in the hemostasis laboratory, for coagulation and/or fibrinolysis testing. Part Number: 0001000311
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1296-2023·2023-04-05

    PCRopsis Reagent Buccal Kit Recalled for Misleading Label Statements

    Entopsis, Inc. is recalling PCRopsis Reagent Buccal (REF 282001), an extraction-free PCR reagent kit, due to misleading label statements on the product labeling.

    Product
    PCRopsis Reagent Buccal, IVD, REF 282001; Extraction-free PCR from bucca; swabs (no transport medium) ,nucleic acid extraction from a variety of biological samples
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V238000·2023-04-04

    Tie rod fastener defect in commercial trucks risks steering failure

    Daimler Trucks is recalling commercial vehicles with a tie rod that may be missing a fastener, allowing the steer arm to detach and causing potential loss of steering control.

    Product
    FCCC — FCCC, FREIGHTLINER, WESTERN STAR MT50E, 114SD, M2, 4700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V237000·2023-04-04

    Freightliner and FCCC trucks recalled for windshield wiper linkage failure

    Daimler Trucks North America is recalling certain 2020-2022 Freightliner and FCCC trucks due to windshield wiper linkage failure that can reduce visibility. Dealers will inspect and replace affected parts free of charge.

    Product
    FREIGHTLINER — FREIGHTLINER, FCCC M2, S2C, S2RV, S2G
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E030000·2023-04-04

    Cummins Recalls Onan Generator Sets Due to Fuel Hose Fire Risk

    Cummins is recalling certain Onan QG 2800i generator sets because a fuel hose may not be properly secured, creating a gas leak and fire risk.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E029000·2023-04-03

    Cruise Recalls Autonomous Driving Software Due to Crash Risk

    Cruise LLC is recalling certain Automated Driving Systems with specific software versions that may inaccurately predict the movement of articulated vehicles, increasing the risk of a crash.

    Product
    ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E027000·2023-03-31

    Lippert Recalls WAY Solar Panels With Insufficient Installation Hardware

    Lippert is recalling WAY Solar Panels because mounting hardware may become loose and pull through the panel slot, potentially causing the panels to detach from the vehicle during transit.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V227000·2023-03-31

    Forest River Recalls 2023 East to West Travel Trailers Due to Drawbar Defect

    Forest River is recalling 2023 East to West Della Terra and Silver Lake travel trailers because the drawbar assembly may break, potentially allowing the trailer to detach.

    Product
    EAST TO WEST — EAST TO WEST DELLA TERRA, SILVER LAKE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V235000·2023-03-31

    Tesla Recalls 2018-2019 Model 3 Vehicles for Suspension Fastener Issue

    Tesla is recalling 2018-2019 Model 3 vehicles because front suspension fasteners may loosen, potentially causing the lateral link to separate and increasing crash risk.

    Product
    TESLA — TESLA MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E028000·2023-03-31

    Felling Trailers Recall Warn Winch Remotes Due to Water Intrusion Risk

    Felling Trailers is recalling 2022-2023 trailers equipped with Warn winches because water may enter the remote control, causing corrosion and unintentional winch operation.

    Product
    FELLING — FELLING DECK-OVER, DROP-DECK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V233000·2023-03-31

    2022 and 2023 Rivian R1S Reverse Lights May Have Reduced Visibility

    Rivian is recalling certain 2022 and 2023 R1S vehicles because the reverse light beam may not be visible from certain angles, increasing the risk of a crash.

    Product
    RIVIAN — RIVIAN R1S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V232000·2023-03-31

    Mercedes-Benz Recalls 2023 AMG CLA 45 Vehicles for Tire Air Leaks

    Mercedes-Benz is recalling 2023 AMG CLA 45 vehicles because tires may leak air, which could cause a loss of vehicle control and increase the risk of a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG CLA45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V234000·2023-03-31

    2021–2023 Winnebago Ekko motorhomes recalled for electrical fire risk

    Winnebago is recalling certain 2021–2023 Ekko motorhomes due to improperly routed wires and loose electrical connections in the 12-volt charging system that can cause fires.

    Product
    WINNEBAGO — WINNEBAGO EKKO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V236000·2023-03-31

    2022 and 2023 Kia Carnival power sliding doors auto-reverse failure

    Kia is recalling 2022 and certain 2023 Carnival vehicles because the power sliding doors' auto-reverse feature may not activate in all situations, risking occupant injury.

    Product
    KIA — KIA CARNIVAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V231000·2023-03-31

    Gulf Stream Recalls 2023-2024 Conquest and BT Cruiser Motor Homes

    Gulf Stream is recalling 2023-2024 Conquest and BT Cruiser motor homes because the entry door latch may fail, preventing entry or exit.

    Product
    GULF STREAM — GULF STREAM CONQUEST, BT CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V226000·2023-03-31

    2023 Forest River Cherokee Travel Trailers Safety Chain Recall

    Forest River is recalling certain 2023 Cherokee CKT36FBOP Travel Trailers because the safety chains may be insufficient for the Gross Vehicle Weight Rating listed on the federal placard, allowing the trailer to detach and increase crash risk.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide