The Recall Desk

State

American Samoa product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46826–46850 of 73849

  • HighFDA (Devices)·Z-2647-2016·2016-08-31

    Bovie Precise 360 Handpiece Recalled for Incomplete Tip Bonding

    Bovie Medical Corporation is recalling 95 units of the BVX-330NR Bovie Precise 360 Handpiece due to potential incomplete bonding of the angled tip.

    Product
    BVX-330NR Bovie Precise 360 Handpiece 33cm, needle Product is used for the delivery of helium gas plasma for cutting, coagulation, and ablation of soft tissue during open and laparoscopic surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2646-2016·2016-08-31

    Bovie Precise 360 Handpiece Recalled Due to Adhesive Bonding Defect

    Bovie Medical Corporation is recalling 95 units of the BVX-330BR Bovie Precise 360 Handpiece because the adhesive bond to the angled tip may be incomplete.

    Product
    BVX-330BR Bovie Precise 360 Handpiece 33cm, blade Product is used for the delivery of helium gas plasma for cutting, coagulation, and ablation of soft tissue during open and laparoscopic surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1973-2016·2016-08-31

    La Torre Copito Marshmallow Chocolate Cookie Recalled for Milk Allergen Mislabeling

    La Torre Foods is recalling Copito Marshmallow Chocolate Cookies because the label lists calcium caseinate but fails to declare milk, a major allergen.

    Product
    la Torre Copito Marshmallow Chocolate Cookie NET WT 4.94 oz packaged in a cardboard box.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2658-2016·2016-08-31

    Philips Ingenuity Core128 CT Systems Recalled for Image Reconstruction Defect

    Philips is recalling three Ingenuity Core128 CT systems because a software upgrade can cause planned anatomy to be cut off in gated helical scan images.

    Product
    Ingenuity Core128, Model number 728323 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16771·2016-08-31

    Salewa Recalls Wild Country Syncro Climbing Harnesses Due to Fall Hazard

    Salewa North America is recalling Wild Country Syncro climbing harnesses because excess materials on the waist belt tab can cause the harness to loosen, posing a fall hazard.

    Product
    Wild Country Syncro Harnesses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1948-2016·2016-08-31

    Montana Flour & Grains Recalls Organic Spelt Grain for Wheat Mislabeling

    Montana Flour & Grains is recalling 100% Organic Spelt Grain because the label fails to declare wheat, a major allergen.

    Product
    100% Organic Spelt Grain, packaged in 10 lbs., 25 lbs. and 50 lbs paper bags, bulk container.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1462-2016·2016-08-31

    Talon Compounding Pharmacy Recalls Human Chorionic Gonadotropin Injection Due to Sterility Concerns

    Talon Compounding Pharmacy is recalling 6,500 vials of Human Chorionic Gonadotropin Injection nationwide due to a lack of assurance of sterility.

    Product
    Human Chorionic Gonadotropin Injection (a) 2500 iu, (b) 2500 iu with B12, (c) 3500 iu, (d) 5000 iu, (e) 5000 iu with B12, (f) 6000 iu, (g) 7500 iu, (h) 7500 iu with B12, (i)11,000 iu, (j)11,000 iu with B12, (k) 15,000 iu, (l) 20,000 iu, (m) 20,000 iu with B12, 10 mL sterile…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·16V631000·2016-08-31

    Thomas Built Buses Recall Wheelchair Lifts Due to Bearing Defect

    Daimler Trucks is recalling 2015-2017 Thomas Built Buses equipped with certain Ricon wheelchair lifts because pivot holes may allow bearings to move, risking platform failure.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2, SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V633000·2016-08-31

    Peterbilt 567 Truck Recalled for Tripping Hazard on Left Rail

    PACCAR is recalling one 2017 Peterbilt 567 truck because a bracket protrudes upward, creating a tripping hazard. Dealers will move the connections to the right rail free of charge.

    Product
    PETERBILT — PETERBILT 567
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2648-2016·2016-08-31

    Bovie Precise 360 Handpiece Recalled for Incomplete Adhesive Bond

    Bovie Medical Corporation is recalling 95 units of the BVX-450BR Bovie Precise 360 Handpiece because the adhesive bond to the angled tip may be incomplete.

    Product
    BVX-450BR Bovie Precise 360 Handpiece 45cm, blade Product is used for the delivery of helium gas plasma for cutting, coagulation, and ablation of soft tissue during open and laparoscopic surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V629000·2016-08-31

    Thomas Built Buses Recall Wheelchair Lifts Due to Bearing Defect

    Daimler Trucks North America is recalling 2015-2017 Thomas Built Buses equipped with specific Ricon wheelchair lifts. Defective pivot holes may allow bearings to move, causing the lift platform to fall and injure the operator.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX, SAF-T-LINER EFX, MINOTOUR, SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1950-2016·2016-08-31

    Montana Flour Recalls Organic White Flour for Undeclared Wheat

    Montana Flour & Grains, Inc. is recalling 100% Organic Unbleached White Flour because the label does not declare wheat, a major food allergen.

    Product
    100% Organic Unbleached White Flour, packaged in 10 lbs., 25 lbs. and 50 lbs paper bags, bulk container.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1949-2016·2016-08-31

    Montana Flour & Grains Recalls Organic Spelt Flour for Undeclared Wheat

    Montana Flour & Grains is recalling 100% Organic Spelt Flour because the label does not declare wheat, a major food allergen.

    Product
    100% Organic Spelt Flour, packaged in 10 lbs., 25 lbs. and 50 lbs paper bags, bulk container.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1970-2016·2016-08-31

    Nabisco Honey Maid Teddy Grahams Cinnamon Cubs Recalled for Peanut Residue

    Mondelez International is recalling Nabisco Honey Maid Teddy Grahams Cinnamon Cubs because they were produced using flour containing peanut residue.

    Product
    Nabisco Honey Maid Teddy Grahams Cinnamon Cubs Graham Snacks Net Wt .5 oz (14g) Distributed by Mondelez Global LL East Hanover, NJ 07936 USA UPC 019320016769
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2657-2016·2016-08-31

    Philips Ingenuity Core CT Systems Recalled for Image Reconstruction Defect

    Philips is recalling 30 Ingenuity Core CT systems because a software upgrade can cause planned anatomy to be cut off in gated helical scans.

    Product
    Ingenuity Core, Model number 728321 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2628-2016·2016-08-31

    GE OEC UroView 2800 Fluoroscopic X-Ray System Recalled for Monitor Firmware Issue

    GE OEC Medical Systems is recalling 47 OEC UroView 2800 fluoroscopic x-ray systems because a firmware issue may cause the LCD workstation monitor to appear dark with no video displayed.

    Product
    OEC UroView 2800, fluoroscopic x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2629-2016·2016-08-31

    GE OEC 9800 Fluoroscopic X-Ray System Recalled for Monitor Firmware Issue

    GE OEC Medical Systems is recalling 47 OEC 9800 fluoroscopic x-ray systems because a firmware issue may cause the LCD workstation monitors to appear dark with no video displayed.

    Product
    OEC 9800, fluoroscopic x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1470-2016·2016-08-31

    Teva Recalls Amoxicillin Oral Suspension Due to Potency Issues

    Teva North America is recalling Amoxicillin for Oral Suspension because stability testing showed the drug was superpotent.

    Product
    AMOXICILLIN — AMOXICILLIN (AMOXICILLIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2656-2016·2016-08-31

    Philips Brilliance CT 16 Power Software Defect Recall

    Philips is recalling 50 Brilliance CT 16 Power systems due to a software defect that may cause planned anatomy to be cut off in images, potentially requiring a rescan.

    Product
    Brilliance CT 16 Power, Model number 728240 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2655-2016·2016-08-31

    Philips Brilliance 16 CT Scanner Recalled for Image Reconstruction Defect

    Philips Medical Systems is recalling 192 Brilliance 16 CT scanners because a software upgrade can cause planned anatomy to be cut off in images, potentially requiring a rescan.

    Product
    Brilliance 16, Model number 728246 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2653-2016·2016-08-31

    Philips Brilliance CT Big Bore Oncology Software Recall

    Philips is recalling 33 Brilliance CT Big Bore Oncology systems due to a software defect that may cause planned anatomy to be cut off in gated helical CT images.

    Product
    Brilliance CT Big Bore Oncology, Model number 728243 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2652-2016·2016-08-31

    Philips Brilliance 64 CT Scanner Recalled for Image Reconstruction Errors

    Philips is recalling 283 Brilliance 64 CT scanners because a software update can cause planned anatomy to be cut off in images, potentially requiring a rescan.

    Product
    Brilliance 64 CT Model number 728231 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide