The Recall Desk

State

American Samoa product recalls

73,388 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 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21651–21675 of 73413

  • ModerateFDA (Drugs)·D-0579-2022·2022-03-02

    Acetaminophen Oral Suspension Recalled for Contaminated Excipient

    Perrigo is recalling Acetaminophen Oral Suspension Grape Flavor (160 mg/5 mL, 16 fl oz bottles) nationwide because the product was manufactured with a contaminated excipient that was recalled by the excipient supplier.

    Product
    Acetaminophen Oral Suspension Grape Flavor, 160 mg per 5 mL, 16 fl oz (473 mL) per bottle, Distributed by Perrigo, Allegan, MI 49010. NDC: 50941-009-43
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0628-2022·2022-03-02

    Nasal Spray Oxymetazoline HCl Recalled Due to Contaminated Excipient

    Perrigo Company PLC is recalling Nasal Maximum Strength Nasal Spray (Oxymetazoline HCl 0.05%) due to contamination from a recalled excipient used during manufacturing. Approximately 2,302 bottles were distributed nationwide.

    Product
    NASAL — NASAL (OXYMETAZOLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0580-2022·2022-03-02

    Equate Children's Pain and Fever Acetaminophen Suspension Recall

    Perrigo Company is recalling Equate Children's Pain and Fever Acetaminophen Suspension (160mg/5ml) due to contaminated excipient used in manufacturing. Approximately 117,552 bottles distributed nationwide are affected.

    Product
    EQUATE CHILDRENS PAIN AND FEVER — EQUATE CHILDRENS PAIN AND FEVER (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0625-2022·2022-03-02

    TOPCARE NASAL Oxymetazoline HCl Recalled Due to Contaminated Excipient

    Perrigo Company PLC is recalling TOPCARE NASAL (Oxymetazoline HCl 0.05%) nasal spray nationwide because products were manufactured with a contaminated excipient obtained from a supplier whose material was recalled.

    Product
    TOPCARE NASAL — TOPCARE NASAL (OXYMETAZOLINE HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0608-2022·2022-03-02

    Nasal Oxymetazoline Spray Recalled for Contaminated Excipient

    Perrigo Company is recalling approximately 9,888 bottles of NASAL Severe Congestion Nasal Spray due to contamination from a recalled excipient used during manufacturing. The product was distributed nationwide.

    Product
    NASAL — NASAL (OXYMETAZOLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0597-2022·2022-03-02

    Parents Choice Infant Acetaminophen Recalled for Contaminated Excipient

    Perrigo Company is recalling approximately 55,656 bottles of Parents Choice Infants Pain and Fever (Acetaminophen) oral suspension nationwide due to CGMP deviations. The product was manufactured with a contaminated excipient that was recalled from the supplier.

    Product
    PARENTS CHOICE INFANTS PAIN AND FEVER — PARENTS CHOICE INFANTS PAIN AND FEVER (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0615-2022·2022-03-02

    Nasal Mist Oxymetazoline HCl Recalled for Contaminated Excipient

    Perrigo Company PLC is recalling approximately 64,512 bottles of NASAL MIST oxymetazoline nasal decongestant distributed nationwide because they were manufactured with a contaminated excipient recalled from the supplier.

    Product
    NASAL MIST — NASAL MIST (OXYMETAZOLINE HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E015000·2022-03-01

    Marion Body Works Recalls Emergency Vehicles Due to Fuel Leak Risk

    Marion Body Works is recalling specific 2018-2021 emergency vehicles because a fuel rail defect may cause leaks, increasing fire risk.

    Product
    MARION BODY WORKS — MARION BODY WORKS FREIGHTLINER M2, KENWORTH T3 SERIES, INTERNATIONAL SR525
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-03012022-01·2022-03-01

    Ready-to-Eat Meat Products Recalled for Undeclared Wheat Allergen

    USDA FSIS issued a public health alert for ready-to-eat meat products containing a seasoning mix with undeclared wheat. Consumers are advised not to consume these items.

    Product
    FSIS Issues Public Health Alert for Ready-to-Eat Meat Products Containing FDA-Regulated Seasoning Mix That Has Been Recalled Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·22V116000·2022-03-01

    Pierce Arrow XT Firetruck Recall for Improperly Crimped Lifting Cables

    Pierce Manufacturing is recalling one 2021 Arrow XT firetruck because improperly crimped lifting cables could cause the generator set to fall, increasing injury risk.

    Product
    PIERCE — PIERCE ARROW XT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V114000·2022-02-28

    Proterra buses recalled for loose steering gearbox securing bolts

    Proterra is recalling 2017-2022 Catalyst and ZX5 buses because steering gearbox securing bolts may loosen due to insufficient adhesive, risking loss of steering control. Owner notifications were sent October 7, 2022.

    Product
    PROTERRA — PROTERRA ZX5, CATALYST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V112000·2022-02-25

    Mercedes-Benz Recalls 2022 EQS Models Due to Electrical Fire Risk

    Mercedes-Benz is recalling 2022 EQS 450, EQS 580, and AMG EQS 53 vehicles because improperly secured electrical connections may increase the risk of a fire or cause headlight failure.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQS 580, EQS 450, AMG EQS 53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V109000·2022-02-24

    Ford Recalls 2021 Escape Hybrid Vehicles Due to Crankshaft Defect

    Ford is recalling 2021 Escape Hybrid vehicles because an incorrectly manufactured engine crankshaft may cause engine damage, leading to stalling or fire.

    Product
    FORD — FORD ESCAPE HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V108000·2022-02-24

    Tenco Recalls One TOR DR-106100 Highway Carrier for Fuel Leak Risk

    Tenco Inc. is recalling one 2020 TOR DR-106100 highway carrier because fuel tubes may crack, causing a high-pressure fuel leak that increases fire risk.

    Product
    TOR — TOR DR-106100
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V107000·2022-02-24

    2021 Toyota C-HR: Inoperative Radar Sensor Disables Collision Avoidance

    Certain 2021 Toyota C-HR vehicles have a radar sensor that was not activated during production, disabling the pre-collision system and forward collision avoidance. Dealers will activate the sensor at no cost.

    Product
    TOYOTA — TOYOTA C-HR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22731·2022-02-24

    Kelly Wynne Children's Handbags Recalled for Excess Lead Content

    Kelly Wynne is recalling about 1,050 Mama & Me MINI children's handbags sold online from July 2020 through October 2021 because metal components contain lead levels that exceed the federal ban. No injuries have been reported.

    Product
    Mama & Me MINI Children's Handbags
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V110000·2022-02-24

    Yamaha Recalls 2021 Tracer 9 GT Motorcycles Due to Throttle Grip Defect

    Yamaha is recalling 453 2021 Tracer 9 GT motorcycles because the throttle grip may break if used to lift the bike, potentially causing loss of throttle control and a crash.

    Product
    YAMAHA — YAMAHA TRACER 9 GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V111000·2022-02-24

    Missing Mounting Bolt in 2022 INFINITI QX60 Second-Row Seat Track

    Nissan is recalling 2022 INFINITI QX60 vehicles because the second-row seat track may be missing a mounting bolt. This could allow the seat track to move during a crash, increasing injury risk.

    Product
    NISSAN — NISSAN, INFINITI PATHFINDER, QX60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0648-2022·2022-02-23

    HCG 6,000iu Injection Recalled for Bacterial Contamination

    Revive Rx is recalling HCG 6,000iu injectable medication due to bacterial contamination (Paenibacillus lautus) identified in the product. The affected lot was distributed nationwide.

    Product
    HCG 6,000iu (lyo) Human Chorionic Gonadotropin Inj., For Sub-Q or IM Use Only, Not For IV Use, Vial, Rx Only, Compounded By: Revive Rx 3831 Golf Dr., Houston, TX 77018, NDC: 88888-1739-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0638-2022·2022-02-23

    RED MAMMOTH 400 mg Capsules Recalled for Undeclared Active Pharmaceutical Ingredients

    RED MAMMOTH capsules, 400 mg (Lot # DK1027, Exp. 08/01/2023) are being recalled because they contain undeclared sildenafil and tadalafil, making them an unapproved drug marketed without FDA authorization.

    Product
    RED MAMMOTH capsules, 400 mg, packaged in 10-count blisters per carton, ASIN B00KA8FBNI, barcode X001ANE0I5.
    Category
    Drug
    Distribution
    Distributed nationwide