The Recall Desk

State

American Samoa product recalls

73,596 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 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28701–28725 of 73621

  • ModerateFDA (Devices)·Z-2190-2020·2020-06-10

    Osteomed Recalls Osteovation Bone Void Filler Kits Due to Shelf-Life Error

    Osteomed, LLC is recalling Osteovation 10 CC Impact Formula bone void filler kits because the labeled shelf-life may be incorrect, potentially affecting the product's setting characteristics.

    Product
    OSTEOVATION 10 CC IMPACT FORMULA. REF/UDI: 390-2110/ /00813845021092 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2201-2020·2020-06-10

    Trividia True Metrix Air Blood Glucose Meter Recall for Unit Error

    One True Metrix Air blood glucose meter is being recalled because it displays results in mmol/L instead of mg/dL.

    Product
    TRUE METRIX SELF MONITORING BLOOD GLUCOSE SYSTEM - Product Usage: is intended for the quantitative measurement of glucose (sugar) in fresh capillary whole blood samples drawn from the fingertip or forearm.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2187-2020·2020-06-10

    Osteomed Recalls Osteovation 3CC ImpactFormula Bone Void Filler Kits

    Osteomed is recalling 409 units of Osteovation 3CC ImpactFormula bone void filler kits due to incorrect shelf-life labeling that may affect product setting characteristics.

    Product
    OSTEOVATION 3CC IMPACTFORMULA. REF/UDI: 390-2103/00813845020078 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2250-2020·2020-06-10

    Nobel Biocare Recalls Dental Implant Healing Abutments Due to Sizing Error

    Nobel Biocare is recalling specific dental implant healing abutments because they were packaged with the wrong size device.

    Product
    Healing Abutment Conical Connection RP 0 3.6 x 5mm, REF: 36644, UDI: 07332747034462 - Product Usage: Dental implant abutments are intended to be used in the upper or lower jaw and used for supporting tooth replacements to restore chewing function. The Healing Abutment is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2184-2020·2020-06-10

    Osteomed Recalls Osteovation Bone Void Filler Due to Shelf-Life Error

    Osteomed is recalling 436 units of Osteovation 10cc Inject Formula because the labeled shelf-life may be incorrect, potentially affecting the product's setting characteristics.

    Product
    OSTEOVATION 10CC INJECT FORMULA. REF/UDI: 390-2010/00813845020061 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1284-2020·2020-06-10

    Triova Recalls Estriol USP Micronized 5 G Due to Impurities

    Triova Pharmaceuticals is recalling Estriol USP Micronized 5 G because the product failed specifications for organic impurities.

    Product
    Estriol USP Micronized 5 G, Rx only, Triova 115 W 3rd Street Suite 720 Tulsa, OK 74103, NDC 71092-9977-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1286-2020·2020-06-10

    Teva Recalls Mixed Amphetamine Salts Tablets Due to Strength Variations

    Teva Pharmaceuticals is recalling 41,348 bottles of 15 mg Mixed Amphetamine Salts tablets because some bottles may contain mixed strengths.

    Product
    DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2245-2020·2020-06-10

    Philips Chest Pneumograph Recalled for Missing Natural Rubber Latex Labeling

    Philips is recalling 1,075 Chest Pneumograph units because the labeling fails to state that the product contains natural rubber latex.

    Product
    Magnetic Resonance Imaging Diagnostic Device accessory - Product Usage: The chest pneumograph (also referred to as the pneumatic bellows, respiration bellows, or respiration sensor) monitors bellows-derived respiration by detecting abdominal or chest wall motion. The chest…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2181-2020·2020-06-10

    Osteomed Recalls Osteovationex Bone Void Filler Due to Shelf-Life Error

    Osteomed, LLC is recalling Osteovationex 3cc Inject Formula bone void fillers because the product may not maintain its setting characteristics for the labeled shelf-life duration.

    Product
    OSTEOVATIONEX 3CC INJECT FORMULA. REF/UDI: 390-0003/00813845020016 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2169-2020·2020-06-10

    FDA Recalls Sterile Custom Surgical Packs from Unregistered Facility

    American Contract Systems is recalling 2,868 sterile custom surgical packs because they were manufactured in a facility not registered by the FDA.

    Product
    Sterile Custom Packs to be used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2182-2020·2020-06-10

    Osteomed Recalls Osteovationex Bone Void Filler Due to Shelf-Life Error

    Osteomed, LLC is recalling 647 units of Osteovationex 5cc Inject Formula because the labeled shelf-life may be incorrect, potentially affecting the product's setting characteristics.

    Product
    OSTEOVATIONEX 5CC INJECT FORMULA. REF/UDI: 390-0005/00813845020023 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2185-2020·2020-06-10

    Osteomed Recalls Osteovationex Bone Void Filler Due to Shelf-Life Error

    Osteomed is recalling 300 units of Osteovationex 5cc ImpactFormula bone void filler kits because the labeled shelf-life may be incorrect, potentially affecting the product's setting characteristics.

    Product
    OSTEOVATIONEX 5CC IMPACTFORMULA. REF/UDI: 390-0205/00813845020047 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2178-2020·2020-06-10

    FDA Recalls Sterile Custom Surgical Packs Due to Unregistered Facility

    American Contract Systems is recalling 2,868 sterile custom surgical packs because they were manufactured in a facility not registered with the FDA.

    Product
    Sterile Custom Packs to be used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2180-2020·2020-06-10

    Osteomed Recalls Osteovationex Bone Void Filler Due to Shelf-Life Error

    Osteomed, LLC is recalling 70 units of Osteovationex 2cc Inject Formula because the product may not maintain its setting characteristics for the labeled shelf-life duration.

    Product
    OSTEOVATIONEX 2CC INJECT FORMULA. REF/UDI: 390-0002/00813845020009 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2251-2020·2020-06-10

    Abbott Accelerator APS Aliquoter Module Recalled for Sample Dilution Risk

    Abbott is recalling 11 Accelerator APS Aliquoter Modules because a clot detection error may cause distilled water to dilute samples, leading to incorrect clinical results.

    Product
    Accelerator APS Aliquoter Module, List number: 07L40 - Product Usage: The ACCELERATOR APS Workcell is a modular system designed to automate sample handling and processing in the clinical laboratory. The system allows consolidations of multiple clinical chemistry and immunoassay…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V340000·2020-06-09

    Mercedes-Benz Metris Recall for Driveshaft Attachment Defect

    Daimler Vans USA is recalling 2019 Mercedes-Benz Metris vans because the driveshaft may not be attached correctly, risking loss of drive or unexpected airbag deployment.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V337000·2020-06-09

    Jayco Recalls 2020 Motorized RVs Due to Window Glass Detachment Risk

    Jayco is recalling 2020 motorized recreational vehicles because the adhesive on frameless windows may fail, allowing glass to detach and become a projectile.

    Product
    JAYCO — JAYCO, ENTEGRA REDHAWK, QWEST, SENECA, EMBLEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V335000·2020-06-09

    ARBOC Spirit of America and Liberty Buses Recalled for Fire Risk

    ARBOC is recalling 113 Spirit of America and Spirit of Liberty buses because misrouted power cables may short circuit, increasing the risk of a fire.

    Product
    ARBOC — ARBOC SPIRIT OF AMERICA, SPIRIT OF LIBERTY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V334000·2020-06-09

    Chrysler Recalls 2017-2020 Pacifica Plug-in Hybrids for Fire Risk

    Chrysler is recalling 2017-2020 Pacifica Plug-in Hybrids because a high-resistance electrical connection may overheat and cause a fire.

    Product
    CHRYSLER — CHRYSLER PACIFICA PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V338000·2020-06-09

    Highland Ridge RV Recalls 2020 Trailers Due to Window Glass Detachment Risk

    Highland Ridge RV is recalling 80 units of 2020 Ridge, Open Range, and Silverstar trailers because window glass may detach and become a projectile.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW MESA RIDGE, OPEN RANGE, SILVERSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V339000·2020-06-09

    2020 Thor Motor Coach motorhome frameless windows may detach while driving

    Thor Motor Coach is recalling certain 2020-2021 motorhomes because the adhesive bond in frameless windows may fail, allowing the glass to detach and become a projectile hazard while the vehicle is in motion.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH AXIS, COMPASS, DELANO, GEMINI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V336000·2020-06-09

    Jayco Recalls 2020 Recreational Vehicles Due to Window Glass Detachment Risk

    Jayco is recalling 2020 Eagle, Jay Flight, and other models because window glass may detach and become a projectile.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL, JAYCO TRAVEL TRAILER EAGLE, JAY FLIGHT, EAGLE HT, NORTH POINT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V333000·2020-06-09

    Lion Recalls 2012-2020 School Buses for Seat Belt Anchor Defect

    Lion Electric Company is recalling 2012-2020 Lion 360 and Lion C school buses because the driver's seat belt anchor may be attached with incorrect hardware, potentially compromising safety in a crash.

    Product
    LION — LION LIONC, 360
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V331000·2020-06-08

    Ford Recalls Vehicles Due to Door Latch Repair Defects

    Ford is recalling specific 2011-2016 vehicles because previous door latch repairs may have been incomplete, potentially allowing doors to open while driving.

    Product
    FORD — FORD, LINCOLN C-MAX, FIESTA, FOCUS, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide