The Recall Desk

State

American Samoa product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50226–50250 of 73852

  • SevereNHTSA·16V024000·2016-01-21

    Rosenbauer Commander Fire Trucks Recalled for Steering Control Loss Risk

    Rosenbauer is recalling 2014-2015 Commander fire trucks because loose ball joints in certain front suspension assemblies could separate, causing a loss of steering control.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V026000·2016-01-21

    Winnebago Recalls 2015-2016 Motorhomes Due to Ignition Switch Defect

    Winnebago is recalling 2015-2016 Travato, Trend, and Itasca Viva! motorhomes because an ignition switch defect may cause the vehicle to stall or disable safety systems.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA TREND, TRAVATO, VIVA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V025000·2016-01-21

    Vanguard Recalls 2014-2015 Dry Freight Van Trailers Due to Brake Drag

    Vanguard is recalling 2014-2015 Dry Freight Van Trailers because improperly seated brake diaphragms may cause drag, potentially leading to wheel end fires.

    Product
    VANGUARD — VANGUARD DRY FREIGHT VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E004000·2016-01-21

    Meritor Trailer Axle Recall for Brake Drag Fire Risk

    Meritor is recalling certain trailer axle assemblies equipped with specific air brake actuators that may experience brake drag, posing a risk of wheel end fire.

    Product
    SERVICE BRAKES, AIR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16081·2016-01-21

    Britax Recalls B-Safe 35 Infant Car Seats Due to Handle Crack Hazard

    Britax is recalling about 71,000 B-Safe 35 infant car seats because the carry handle can crack and break, posing a fall hazard to infants.

    Product
    Britax B-Safe 35 and B-Safe 35 Elite infant car seats and travel systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16723·2016-01-21

    Chillafish Recalls Children's Balance Bikes Due to Laceration Hazard

    Chillafish is recalling BMXie, Jack, and Josie balance bikes because overinflated tires can cause plastic rims to crack and send pieces flying, posing a laceration hazard.

    Product
    Children's bikes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·007-2016·2016-01-20

    Snapp's Ferry Packing Recalls Beef Product Due To Possible E. Coli O157:H7

    Snapp's Ferry Packing Company is recalling approximately 410 pounds of ground beef that may be contaminated with E. coli O157:H7.

    Product
    SAN Meat Packing Inc. — Snapp's Ferry Packing Company Recalls Beef Product Due To Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0503-2016·2016-01-20

    Nestle Recalls Sweet Leaf Lemonade Tea Due to Glass Particles

    Nestle Waters North America is recalling Sweet Leaf Organic Half and Half Lemonade Tea because the product contains glass particles.

    Product
    Sweet Leaf Organic Half and Half Lemonade Tea, 16 oz glass bottle UPC: 6-51538-06708-1
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V020000·2016-01-20

    MCI Recalls Buses Due to Potential Seat Belt Anchor Weld Defects

    Motor Coach Industries is recalling specific MCI buses because missing welds on driver seat brackets could allow seat belt anchors to separate, increasing injury risk in a crash.

    Product
    MCI — MCI D4000, D4500, J4500, D4505
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0641-2016·2016-01-20

    Ortho-Clinical VITROS 5600 Chemistry System Software Recall

    Ortho-Clinical Diagnostics is recalling VITROS 5600 Chemistry Systems due to a software anomaly that may cause erroneous test results without user notification.

    Product
    VITROS 5600 Chemistry System, Catalog Number 6802413, Unique Device Identifier Number 10758750009916, Software Product Code 6802864, Software Version 3.2 and below; IVD. Product Usage: For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0504-2016·2016-01-20

    Sweet Leaf Organic Sweet Tea Recalled for Glass Particles

    Nestle Waters North America is recalling Sweet Leaf Organic Original Sweet Tea because the product contains glass particles.

    Product
    Sweet Leaf Organic Original Sweet Tea, 16 oz glass bottle UPC: 6-51538-06700-5
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0644-2016·2016-01-20

    CompView NuCARTGN Medical Display Recall Due to Spring Arm Detachment Risk

    CompView Medical is recalling 10 NuCARTGN mobile display units because the spring arm may detach if the securing ring was not installed correctly.

    Product
    Model NuCARTGN. The NuCART is a mobile display and image management platform used in Minimally Invasive Surgery (MIS) environments to facilitate the routing and ergonomic display of video signals from source devices to flat-panel monitors. It is tailored for use with an OEC…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V023000·2016-01-20

    Altec Recalls Aerial Devices Due to Hydraulic Valve Defect

    Altec is recalling 2010-2015 AH75, AH85, and AH100 aerial devices because a hydraulic valve may allow unexpected movement, increasing injury risk.

    Product
    ALTEC — ALTEC AH100, AH75, AH85
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16079·2016-01-20

    Cheryl's Jingle Bell Ornaments Recalled for Sharp Metal Edges

    Cheryl & Co. is recalling Jingle Bell ornaments sold by QVC because sharp metal edges on the cutouts pose a laceration hazard.

    Product
    Cheryl's Jingle Bell ornaments with cookies and confections
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0507-2016·2016-01-20

    Nestle Recalls Sweet Leaf Organic Tea Mint & Honey Due to Glass Particles

    Nestle Waters North America is recalling Sweet Leaf Organic Tea Mint & Honey because the product contains glass particles.

    Product
    Sweet Leaf Organic Tea Mint & Honey, 16 oz glass bottle UPC: 6-51538-06701-2
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0506-2016·2016-01-20

    Nestle Recalls Sweet Leaf Peach Iced Tea Due to Glass Particles

    Nestle Waters North America is recalling Sweet Leaf All Natural Peach Iced Tea because the product contains glass particles.

    Product
    Sweet Leaf All Natural Peach Iced Tea , 16 oz glass bottle UPC: 6-51538-06704-3
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0648-2016·2016-01-20

    Brainlab RT Elements software recall for image cropping defect

    Brainlab AG is recalling RT Elements software because large objects may display cropped during import, potentially affecting radiation treatment planning.

    Product
    RT Elements are applications for radiation treatment planning for use in stereotactic, conformal, computer planned, Linac based radiation treatment of cranial, head and neck, and extracranial lesions. The simulated plan is intended for treatment evaluation for example in tumor…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0640-2016·2016-01-20

    Ortho-Clinical VITROS 3600 Chemistry System Recalled for Software Anomaly

    Ortho-Clinical Diagnostics is recalling VITROS 3600 Chemistry Systems due to a software anomaly that may allow the device to process assays at incorrect temperatures, potentially producing erroneous results.

    Product
    VITROS 3600 Chemistry System, Catalog Number 6802783, Unique Device Identifier Number 10758750009930, Software Product Code 6802866, Software Version 3.2 and below; IVD. Product Usage: For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0652-2016·2016-01-20

    Intuitive Surgical Recalls da Vinci Xi 8mm Endoscopes for Safety Manual Correction

    Intuitive Surgical is correcting the da Vinci Xi I&A User Manual to prevent unintended patient harm from capacitive coupling when using 8mm endoscopes with specific instruments.

    Product
    0 deg, 8mm Endoscope, IS4000: Model numbers: 470026-34, 470026-40, 470026-41. General and Plastic Surgery: The da Vinci Xi endoscope produces high definition (HD), visible light (VIS). The HD video is processed by the system electronics in the Vision Cart and displayed on…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16E003000·2016-01-20

    GMAX Recalls GM78 Fullface Helmets for Safety Standard Non-Compliance

    GMAX Helmet LLC is recalling specific GM78 Fullface helmets that may not adequately protect users in a crash. Owners can exchange the helmet or receive a refund.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0653-2016·2016-01-20

    Intuitive Surgical Recalls da Vinci Xi Endoscopes for Capacitive Coupling Risk

    Intuitive Surgical is correcting the da Vinci Xi I&A User Manual to warn about unintended patient harm from capacitive coupling when using 8 mm endoscopes with specific instruments.

    Product
    30 deg, 8mm Endoscope, IS4000: Model numbers: 470027-34, 470027-40, 470027-41. General and Plastic Surgery: The da Vinci Xi endoscope produces high definition (HD), visible light (VIS). The HD video is processed by the system electronics in the Vision Cart and displayed on…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0567-2016·2016-01-20

    Freedom Pharmaceuticals Recalls Domperidone API Due to Penicillin Cross-Contamination

    Freedom Pharmaceuticals is recalling specific lots of Domperidone API for prescription compounding due to potential cross-contamination with penicillin.

    Product
    Domperidone BP, Active Pharmaceutical Ingredient for Prescription Compounding, packaged in a) 5 gm (NDC: 52372-0898-01), b) 25 gm (NDC: 52372-0898-02), c) 100 gm (NDC: 52372-0898-03), and d) 500 gm (NDC: 52372-0898-04), Cas No. 57808-66-9, Rx only, FREEDOM, 801 W. New Orleans…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0643-2016·2016-01-20

    Ortho-Clinical VITROS 5,1 FS Chemistry System Software Recall

    Ortho-Clinical Diagnostics is recalling VITROS 5,1 FS Chemistry Systems because a software anomaly may cause the device to process assays at incorrect temperatures, potentially producing erroneous results.

    Product
    VITROS 5,1 FS Chemistry System, Catalog Number 6801375, Unique Device Identifier Number 10758750001132, and VITROS 5,1 FS Chemistry System Refurbished, Catalog Number 6801890, Unique Device Identifier Number 10758750001644, Software Version 2.8 and below, IVD. Product Usage…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0502-2016·2016-01-20

    Sweet Leaf Organic Raspberry Iced Tea Recalled for Glass Particles

    Nestle Waters North America is recalling Sweet Leaf Organic Raspberry Iced Tea because the product contains glass particles.

    Product
    Sweet Leaf Organic Raspberry Iced Tea, 16 oz glass bottle UPC: 6-51538-06703-6
    Category
    Food
    Distribution
    Distributed nationwide