The Recall Desk

State

American Samoa product recalls

73,503 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 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24576–24600 of 73528

  • SevereNHTSA·21E051000·2021-06-14

    Wallace Forge recalls medium duty adjustable mount couplers

    Wallace Forge is recalling specific medium duty adjustable mount couplers that may uncouple due to excessive play, increasing crash risk.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V447000·2021-06-14

    Kia K5 2021-2022 steering system defect increases crash risk

    Kia is recalling certain 2021-2022 K5 models with a power steering defect. The steering system may lose assist while driving due to a communication fault, increasing crash risk.

    Product
    KIA — KIA K5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·21V448000·2021-06-14

    Utilimaster Velocity Recalled for Incorrect Seating Capacity Placard

    Shyft Group is recalling 2021 Utilimaster Velocity vehicles because the tire and loading placard incorrectly states a seating capacity of one instead of two.

    Product
    UTILIMASTER — UTILIMASTER VELOCITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V446000·2021-06-13

    Rossmonster Ram Promaster Recall for Potential Gas Leak Fire Risk

    Rossmonster is recalling 2018 Ram Promaster vans because an overtightened saddle valve bolt may damage the o-ring seal, causing a gas leak that increases fire risk.

    Product
    ROSSMONSTER — ROSSMONSTER RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V445000·2021-06-11

    Host Campers Recalls 2019-2021 Trailers Due to Gas Leak Risk

    Host Industries is recalling 2019-2021 Cascade, Rainier, Tahoe, and Mammoth trailers because a stove bolt may damage the seal, causing a gas leak and fire risk.

    Product
    HOST CAMPERS — HOST CAMPERS TAHOE, RAINIER, CASCADE, MAMMOTH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V443000·2021-06-11

    2021 Forest River Wildwood and Salem Trailer Clearance Lamp Defect

    Forest River is recalling 2021 Wildwood and Salem trailers because red and amber clearance lamps do not reflect enough light. This visibility defect increases the risk of crashes with other vehicles.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V444000·2021-06-11

    2021 East to West Alta Travel Trailers: LP/CO Detector Placement Recall

    Forest River is recalling 2021 East to West Alta travel trailers because the LP/CO detector was installed in the incorrect location. This impairs propane leak and carbon monoxide detection, increasing fire and injury risks.

    Product
    EAST TO WEST — EAST TO WEST ALTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V438000·2021-06-10

    2021 RAM 1500 rearview camera may fail to display, increasing crash risk

    Certain 2021 RAM 1500 vehicles may have a rearview camera that doesn't display due to a software issue in the trailer reverse steering module. This reduces rear visibility and increases the risk of crashes.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V441000·2021-06-10

    Thor Motor Coach Motorhomes Recalled for Missing LP Tank Heat Shield

    Thor Motor Coach is recalling 2018-2022 Axis and 2018-2021 Vegas motorhomes with missing heat shields between the LP tank and chassis muffler. A missing heat shield increases fire risk; dealers will install the shield free of charge.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH VEGAS, AXIS, redundant AXIS, redundant VEGAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V440000·2021-06-10

    Emergency jack fracture risk affects Chevrolet Trailblazer and Buick Encore GX

    General Motors is recalling approximately 135,400 certain 2020-2022 Buick Encore GX and 2021-2022 Chevrolet Trailblazer vehicles because their emergency jacks can fracture if not positioned correctly, risking vehicle collapse.

    Product
    CHEVROLET — CHEVROLET, BUICK TRAILBLAZER, ENCORE GX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21753·2021-06-10

    2021 Can-Am Outlander and Renegade ATVs Recalled for Crash Hazard

    BRP is recalling about 4,600 model year 2021 Can-Am Outlander and Renegade ATVs because the steering knuckle can detach from the lower arm, causing loss of control and crash risk.

    Product
    2021 Can-Am Outlander and Renegade ATVs
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21754·2021-06-10

    Children's Barhee Fishing Hero Toy Games Recalled for Excessive Lead Content

    Blue Star Trading is recalling about 300 Barhee Fishing Hero toy games sold on Amazon.com because metal rollers on the flying dinosaur figures contain lead levels exceeding the federal ban. Lead is toxic to young children if ingested.

    Product
    Children's Barhee Fishing Hero Toy Games
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V421000·2021-06-10

    2021 Buick Envision air bag warning lamp may fail to illuminate

    GM is recalling 2021 Buick Envision vehicles—the air bag warning lamp may fail to illuminate due to a module defect. Owners should contact their dealer for a free software update.

    Product
    CHEVROLET — CHEVROLET, CADILLAC, GMC SUBURBAN, ESCALADE ESV, ESCALADE, YUKON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0627-2021·2021-06-09

    Pfizer Lidocaine and Bupivacaine Injection Label Mix-Up Recall

    Pfizer has recalled 139,050 vials of injectable anesthetic medications due to a label mix-up: some vials labeled as Lidocaine contain Bupivacaine, and some labeled as Bupivacaine contain Lidocaine. Patients and healthcare providers should verify medication identity before use.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V437000·2021-06-09

    Karavan Recalls 2021 Move I 1500 Long Trailers Due to Axle Weld Defect

    Karavan is recalling 2021 Move I 1500 Long trailers because improperly welded wheel spindles can break, causing the wheel to detach and increasing crash risk.

    Product
    KARAVAN — KARAVAN MOVE I 1500 LONG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·21150·2021-06-09

    Klein Tools Non-Contact Voltage Tester Recalled for Shock Hazard

    Klein Tools non-contact voltage testers (model NCVT-1) are recalled because the on/off button can fail to disengage, causing the tester to malfunction and potentially fail to detect live voltage. One shock injury has been reported.

    Product
    Klein Tools Non-Contact Voltage Tester Model NCVT-1
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0626-2021·2021-06-09

    Bupivacaine and Lidocaine Injection Vials Recalled for Label Mix-Up

    Pfizer is recalling 163,957 vials of 0.5% Bupivacaine Hydrochloride Injection due to a label mix-up where some vials labeled as bupivacaine may contain lidocaine, and vials labeled as lidocaine may contain bupivacaine. The mix-up could lead to patients receiving the wrong local anesthetic.

    Product
    BUPIVACAINE HYDROCHLORIDE — BUPIVACAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1712-2021·2021-06-09

    ZVplasty Direct Access Trocar Recalled for Inadequate Sterilization

    Zavation is recalling ZVplasty Direct Access Diamond Tip Trocars (11 Gauge) because some units may not be adequately sterilized. These surgical instruments are used in orthopedic and spinal procedures.

    Product
    ZVplasty Direct Access Diamond Tip Trocar, 11 Gauge, REF VCF-1023-11. For use in Orthopedic / spinal procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1753-2021·2021-06-09

    Orthopedic Spinal Surgery Kit Recalled for Inadequate Sterilization

    Zavation is recalling InterV CurvePlus surgical kits because products distributed as sterile may not have been adequately sterilized. 36 units were distributed nationwide.

    Product
    InterV CurvePlus Kit, REF Numbers: a) INTVMC-15-FLDSK b) INTVMC-20-FLDSK. For use in Orthopedic / spinal procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1775-2021·2021-06-09

    Synapse Cardiovascular software may incorrectly reuse patient database identifiers

    Fujifilm's Synapse Cardiovascular software versions 6.0.4 to 6.2.1 contain a defect in the Advanced Reporting function where previously assigned patient database identification numbers can be reused for new patients when specific patient merge operations are executed.

    Product
    Synapse Cardiovascular (Synapse CV). Software Versions: 6.0 to 6.2.1 The Synapse Cardiovascular image is a management and reporting system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1763-2021·2021-06-09

    ZVplasty 10G FLEX Kyphoplasty Spinal Device Recall Due to Sterilization Failure

    Zavation is recalling 19 units of ZVplasty 10G FLEX KYPHOPLASTY spinal devices because distributed units may not have been adequately sterilized, posing infection risk to patients.

    Product
    ZVplasty 10G, FLEX KYPHOPLASTY, REF VCF-1015-FLEX. For use in Orthopedic / spinal procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide