The Recall Desk

State

American Samoa product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34351–34375 of 73763

  • SevereNHTSA·19V260000·2019-04-01

    Labrie CNG Refuse Trucks Recalled for Valve Stem Ejection Risk

    Labrie is recalling 2017-2018 Automizer and Expert CNG refuse trucks because valve stems may forcibly eject, posing injury and fire risks.

    Product
    LABRIE — LABRIE AUTOMIZER, EXPERT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V261000·2019-04-01

    Eldorado Shuttle Bus Recall for Reversed Backup Camera Image

    Eldorado is recalling 2017-2018 shuttle buses because backup camera displays may revert to factory settings, causing the image to reverse and increasing crash risk.

    Product
    ELDORADO — ELDORADO ADVANTAGE, AEROTECH, AERO ELITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V258000·2019-03-29

    Forest River Recalls 2017-2019 Rockport Work Trucks for Fire Risk

    Forest River is recalling 2017-2019 Rockport work trucks because a missing inline fuse may allow excess current to melt wiring, increasing the risk of a fire.

    Product
    FOREST RIVER — FOREST RIVER ROCKPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V259000·2019-03-29

    Supreme Service Body Vehicles Recalled for Missing Head Impact Padding

    Supreme Corporation is recalling 2014-2018 Service Body vehicles on Ford Transit chassis because they may lack required padded trim for head impact protection.

    Product
    SUPREME — SUPREME SERVICE BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V253000·2019-03-28

    Genie Recalls 2019 TZ-34 and TZ-50 Aerial Devices for Fire Risk

    Genie is recalling 2019 TZ-34 and TZ-50 trailer-mounted aerial devices because improperly crimped battery cables may overheat and cause a fire.

    Product
    GENIE — GENIE TZ-34, TZ-50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V252000·2019-03-28

    Ford Transit Vans Recalled Over Faulty Foldaway Seats

    Waldoch Crafts is recalling 2018 Ford Transit shuttle vans with Freedman GO-ES foldaway seats. The seat cushion may fail to lock in a crash, posing an injury risk.

    Product
    FORD — FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V248000·2019-03-28

    2019 Jeep Cherokee Recalled for Loose Front Passenger Seat Bolts

    Chrysler is recalling 2019 Jeep Cherokee vehicles because loose front passenger seat mounting bolts may allow the seat to move in a crash, increasing injury risk.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V249000·2019-03-28

    Royale Recalls 2015-2017 Mercedes Sprinter Coaches Due to Seat Lock Defect

    Royale is recalling 2015-2017 Mercedes Sprinter-based mini coaches because the rear seat cushion may not stay locked in place during a crash or sudden stop.

    Product
    MERCEDES ROYALE — MERCEDES ROYALE SPRINTER COACH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V256000·2019-03-28

    Acura Recalls MDX Models Due to Tailgate Light Moisture Ingress

    Honda is recalling 2014-2019 Acura MDX and 2017-2019 MDX Sport Hybrid vehicles because moisture may enter the tailgate lid lights, causing them to fail and reducing vehicle visibility.

    Product
    ACURA — ACURA MDX SPORT HYBRID, MDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V251000·2019-03-28

    Fire Equipment Sales Recalls Two Emergency Vehicles With Faulty Brake Lights

    Fire Equipment Sales & Service is recalling two 2018 emergency vehicles because their brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.

    Product
    FORD — FORD, FREIGHTLINER F-550, M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19092·2019-03-28

    Midwest-CBK Recalls Baby Rattle Socks Due to Choking Hazard

    Midwest-CBK is recalling Baby Rattle Socks because small ornaments can detach, posing a choking hazard to young children. No injuries have been reported.

    Product
    Baby Rattle Socks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V250000·2019-03-28

    Road Rescue Ultramedic Recalled for Backup Camera Display Defect

    REV Ambulance Group is recalling 2018-2019 Road Rescue Ultramedic vehicles because backup camera displays may revert to factory settings, causing the image to reverse.

    Product
    ROAD RESCUE — ROAD RESCUE ULTRAMEDIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19094·2019-03-28

    Interline Brands Recalls ProPlus Brass Swivel Fittings Due to Fire Hazard

    Interline Brands is recalling ProPlus Brass Flare Swivel Fittings because they can leak, posing a fire hazard. Consumers should contact Interline for a full refund or replacement.

    Product
    ProPlus Brass Flare Swivel Fittings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1025-2019·2019-03-27

    Advanced Pharma Recalls Glycopyrrolate Injectable Syringes Due to Sterility Concerns

    Advanced Pharma Inc. is recalling 140 syringes of Glycopyrrolate 0.6 mg/3 mL Injectable Solution because the company cannot ensure the product is sterile.

    Product
    Glycopyrrolate 0.6 mg/3 mL (0.2 mg per mL) Injectable Solution, 3 mL Sterile single use syringe, For IV or IM use, NDC: 42852-828-22 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1032-2019·2019-03-27

    Advanced Pharma Recalls Phenylephrine HCl Injectable Solution Due to Sterility Concerns

    Advanced Pharma Inc. is recalling 1,850 syringes of Phenylephrine HCl Injectable Solution nationwide due to a lack of assurance of sterility.

    Product
    Phenylephrine HCl, 1 mg in Sterile Water for Injection, QS 10 mL Injectable Solution 1 mg/10 mL (100 mcg per mL) NDC: 42852-802-61 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1017-2019·2019-03-27

    Advanced Pharma Recalls Fentanyl Injectable Solution Due to Sterility Concerns

    Advanced Pharma Inc. is recalling 360 bags of fentanyl injectable solution nationwide due to a lack of assurance of sterility.

    Product
    fentaNYL 1000 mcg/100 mL Injectable Solution Fentanyl 0.9% Sodium Chloride, QS, 100 mL, Sterile single use bag, NDC: 42852-210-10 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1045-2019·2019-03-27

    AvKARE Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity

    AvKARE Inc. is recalling Losartan Potassium and Hydrochlorothiazide Tablets because an impurity, N-Methylnitrosobutyric acid (NMBA), was identified.

    Product
    Losartan Potassium and Hydrochlorothiazide Tablets, USP 50 mg/12.5 mg 50 Tablets (5x10) Unit Dose boxes, Rx Only Manufactured for: AvKARE Inc. Pulaski, TN 38478 --- NDC 50268-513-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1019-2019·2019-03-27

    Advanced Pharma Recalls Midazolam Injectable Solution Due to Sterility Concerns

    Advanced Pharma Inc. is recalling 1,125 bags of Midazolam Injectable Solution nationwide due to a lack of assurance of sterility.

    Product
    Midazolam Benzodiazepine 50 mg/50 mL (1 mg/mL) Injectable Solution, Midazolam HCl 0.9% Sodium Chloride, QS, Sterile single use bag, NDC: 42852-401-05 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1016-2019·2019-03-27

    Advanced Pharma Recalls Hydromorphone Syringes Due to Sterility Concerns

    Advanced Pharma Inc. is recalling 2,400 syringes of Hydromorphone HCl injectable solution nationwide due to a lack of assurance of sterility.

    Product
    HYDROmorphone HCl 1 mg in 0.9% Sodium Chloride, QS 5 mL Injectable Solution 1 mg/5 mL (0.2 mg per mL), Sterile single use syringe, NDC: 42852-289-67 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
    Category
    Drug
    Distribution
    Distributed nationwide