The Recall Desk

State

American Samoa product recalls

73,187 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 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

14501–14525 of 73212

  • HighFDA (Devices)·Z-2414-2023·2023-08-23

    FreeStyle Libre 2 Readers may fail to activate new sensors

    FreeStyle Libre 2 Readers may display an 'Incompatible Sensor' error when attempting to activate a new sensor after incomplete 14-day wear, potentially preventing new sensor activation and causing delayed glucose monitoring.

    Product
    FreeStyle Libre 2 Readers, REF: 71951-01 and 71953-01, used with FreeStyle Libre 2 System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2413-2023·2023-08-23

    HF Resection Electrodes Recalled for Wire Breakage and Patient Fragment Hazard

    Olympus HF Resection Electrodes are being recalled due to reports of loop wire breakage when contacting metal objects. Broken fragments can fall inside the patient and require retrieval.

    Product
    HF Resection Electrodes - HF resection electrodes are part of a resectoscope system for endoscopic diagnosis and treatment in urological or gynecological applications. 64 Models: 1) A22201C 2) A22201D 3) A22202C 4) A22203C 5) A22205C 6) A22205D 7) A22206C 8)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1084-2023·2023-08-23

    Toothpaste Label Mix-Up: Wrong Tube Labels in Strawberry Cartons

    Hello wild strawberry fluoride toothpaste cartons contain tubes incorrectly labeled as hello fresh watermelon fluoride free toothpaste. 182,046 units affected nationwide.

    Product
    hello wild strawberry fluoride toothpaste, sodium fluoride 0.24% (0.15% w/v fluoride ion), NET WT 4.2 OZ (119 g), Distributed by Hello Products LLC, Montclair, NJ 07042, UPC 8 19156 02026 4 (carton), 12-count case GTIN: 20819156020268; strawberry tubes also sold in Strawberry…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·23V592000·2023-08-23

    Bentley Recalls 2017-2023 Bentayga Vehicles for Fuel Leak Fire Risk

    Bentley is recalling 2017-2023 Bentayga vehicles because fuel supply module wiring can overheat, melt a flange, and cause a fuel leak that increases fire risk.

    Product
    BENTLEY — BENTLEY BENTAYGA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2401-2023·2023-08-23

    UroPass Ureteral Access Sheaths Recalled for Dilator Tip Breakage

    Olympus is recalling UroPass Ureteral Access Sheaths because dilator tips may break during surgical procedures or while in the package. The recall affects 9,520 units manufactured in 2018 and 2019.

    Product
    UroPass Ureteral Access Sheaths, 5 pieces/box
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2405-2023·2023-08-23

    Hip Screw Labeled as Wrong Size: 30mm Screws Mislabeled as 25mm

    Conformis hip screws measuring 30mm have been mislabeled as 25mm, creating risk of incorrect surgical implantation. The recall affects 25 units distributed across nine states.

    Product
    CONFORMIS HIP-SCREW-6.5MM X 25MM, STERILE EO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2407-2023·2023-08-23

    Centurion FMS Pak Recalled Due to Patient Injury Risk from Plastic Debris

    Alcon Research recalls the Centurion FMS Pak following reports of patient injury during procedures. Plastic debris can result from over-tightening with the included plastic wrench.

    Product
    Centurion FMS Pak
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V593000·2023-08-23

    Volkswagen Recalls 2024 Atlas Cross Sport for Engine Bearing Defect

    Volkswagen is recalling 2024 Atlas and Atlas Cross Sport vehicles because engine bearings may fail, causing engine stalls and increasing the risk of crashes and fires.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2412-2023·2023-08-23

    Medtronic ventricular catheter system recalled due to incorrect labeling expiration date

    Medtronic is recalling 44 units of the Duet External Drainage and Monitoring system because the product labels contain an incorrect expiration date. The affected lot (226632942) was distributed nationwide.

    Product
    Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventricular Catheter, STERILE EO, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1086-2023·2023-08-23

    Tobramycin Ophthalmic Solution recalled for failed quality specifications

    Alembic Pharmaceuticals is recalling 82,400 bottles of Tobramycin Ophthalmic Solution nationwide because the product failed to meet impurities and degradation specifications.

    Product
    TOBRAMYCIN OPHTHALMIC SOLUTION — TOBRAMYCIN OPHTHALMIC SOLUTION (TOBRAMYCIN OPHTHALMIC SOLUTION)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1085-2023·2023-08-23

    PLUVICTO Injection Recalled for Incorrect Lot and Expiration Date Labels

    PLUVICTO (lutetium Lu 177 vipivotide tetraxetan) injection vials were labeled with incorrect lot numbers and expiration dates. The manufacturer is recalling affected lots distributed nationwide.

    Product
    PLUVICTO 1,000MBq/mL (27 mCi/mL), lutetium Lu 177 vipivotide tetraxetan injection, 9.2 mL Single-dose vial, Manufacturer: Advanced Accelerator Appllications USA, Inc., 57 E. Willow Street NJ 07041, Milburn, USA, NDC 69488-010-61
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V591000·2023-08-22

    Harley-Davidson Softail Motorcycles Recalled for Faulty Shock Absorber Fastener

    Harley-Davidson is recalling certain 2018–2023 Softail motorcycles where a fastener securing the rear shock absorber may break, causing tire damage and loss of tire pressure. This can lead to loss of vehicle control and increased crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FXLRST, FXRST, FLHC, FLHCS ANV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E062000·2023-08-21

    Outfitter Truck Campers Recalled for Potential Gas Leak Fire Risk

    Outfitter is recalling 2021-2022 truck campers because aluminum burner tubes may fracture, causing a gas leak that could lead to fire.

    Product
    OUTFITTER MANUFACTURING — OUTFITTER MANUFACTURING CARIBOU LITE 6.5, CARIBOU LITE 8.5, APEX 8, CARIBOU 6.5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V589000·2023-08-18

    2021-2023 Hyundai Elantra HEV unintended acceleration software defect

    Hyundai is recalling certain 2021-2023 Elantra HEV vehicles due to a software error in the motor control unit that may cause unintended acceleration after releasing the brake pedal, increasing crash risk.

    Product
    HYUNDAI — HYUNDAI ELANTRA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·23263·2023-08-17

    Zipadee Kids Convertible House Bed Frames Recalled for Entrapment and Strangulation Risk

    Zipadee Kids Convertible House Bed Frames and Montessori Floor Beds are being recalled due to spindle spacing that can trap a child's torso while preventing their head from passing through, creating a strangulation hazard. At least two children have become entrapped.

    Product
    Zipadee Kids Convertible House Bed Frames and Montessori Floor Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23783·2023-08-17

    Ubio Labs power banks recalled due to fire hazard

    Costco is recalling approximately 350,000 Ubio Labs power banks (model PWB1071) that can overheat and ignite. The company has received three fire reports, including one on a commercial flight with four smoke inhalation reports and one minor burn injury.

    Product
    Ubio Labs power banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V588000·2023-08-17

    2023 Honda Accord and CR-V Hybrid transmission defect can cause power loss

    Honda is recalling certain 2023 Accord Hybrid and CR-V Hybrid vehicles because the electronic continuously variable transmission (e-CVT) may have been improperly manufactured, potentially resulting in loss of drive power and increased crash risk.

    Product
    HONDA — HONDA ACCORD HYBRID, CR-V HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23265·2023-08-17

    Simplay3 Toddler Towers Recalled Due to Fall and Injury Hazards

    Simplay3 Toddler Towers can tip over during use, posing fall and injury hazards to young children. The manufacturer has received 16 reports of tipping, including 10 reports of injuries.

    Product
    Simplay3 Toddler Towers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V586000·2023-08-17

    Travel trailer safety chains recalled for trailer detachment risk

    Grand Design is recalling 2022–2024 Momentum travel trailers due to underrated safety chains that may not support the trailer's weight. The defect could allow the trailer to detach from the tow vehicle.

    Product
    GRAND DESIGN — GRAND DESIGN MOMENTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V587000·2023-08-17

    2023 International HV and MV Driveshaft Failure Recall

    Navistar recalls certain 2023 International HV and MV vehicles; driveshafts may break under certain conditions, causing loss of drive power and increasing crash risk. Replacement is free.

    Product
    INTERNATIONAL — INTERNATIONAL MV, HV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23782·2023-08-17

    Midwest Lubricants Sodium Hydroxide Recalled for Unsafe Packaging

    Midwest Lubricants is recalling about 3,000 units of Sodium Hydroxide (Caustic Soda Beads) because the packaging is not child-resistant and the label lacks required hazard information. The product poses a risk of chemical burns and eye irritation.

    Product
    Midwest Lubricants Sodium Hydroxide
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1421-2023·2023-08-16

    Food Recall: ONO Vegan Blueberry Protein Overnight Oats for Undeclared Milk

    ONO LLC is recalling ONO Vegan Blueberry Muffin Protein Overnight Oats because they contain undeclared milk, a common allergen. The product was distributed nationwide and poses a risk to consumers with milk allergies.

    Product
    ONO Vegan Blueberry Muffin Protein Overnight Oats, 2.75oz. UPC 01-95893-47024-2
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·23262·2023-08-16

    Gree Recalls 1.56 Million Dehumidifiers Due to Fire and Burn Hazards

    Gree is recalling approximately 1.56 million dehumidifiers sold under brand names including GE, Kenmore, SoleusAir, Seabreeze, and Norpole because they can overheat, smoke, and catch fire, creating fire and burn hazards.

    Product
    Dehumidifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1401-2023·2023-08-16

    Cava Spicy Hummus recalled nationwide for undeclared sesame

    Cava Spicy Hummus (8oz, UPC 89832800227) is being recalled because it contains undeclared sesame. The product was distributed nationwide; consumers with sesame allergies may be at risk.

    Product
    Cava Spicy Hummus UPC 89832800227 Net Wt. 8oz./226.8 g Packaged in clear plastic container. 12 units per case
    Category
    Food
    Distribution
    Distributed nationwide