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.

47101–47125 of 73849

  • CriticalFDA (Food)·F-1885-2016·2016-08-17

    Let's Do Lunch Turkey Bologna Sandwich Recalled for Listeria Risk

    Let's Do Lunch, Inc. is recalling Turkey Bologna & Cheese Sandwiches due to potential Listeria monocytogenes contamination. The product was distributed nationwide in the U.S.

    Product
    Integrated Food Service Turkey Bologna & Cheese Sandwich Turkey Bologna on a whole Grain French Roll Code #C12001/120001
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1884-2016·2016-08-17

    Let's Do Lunch Recalls Super Sub Sandwiches for Listeria Risk

    Let's Do Lunch, Inc. is recalling Cafe Favorites 5" Super Sub sandwiches due to potential Listeria monocytogenes contamination. The products were distributed nationwide in the U.S.

    Product
    Cafe Favorites 5" Super Sub on a Whole Grain Hoagie-IW Code #C02384/02384
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1890-2016·2016-08-17

    Let's Do Lunch Recalls Submarine Sandwiches for Listeria Risk

    Let's Do Lunch, Inc. is recalling Integrated Food Service Submarine Sandwiches on Whole Grain Ciabatta Rolls due to potential Listeria monocytogenes contamination.

    Product
    Integrated Food Service Submarine Sandwich on a Whole Grain Ciabatta Roll Code #C14006/140006
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1878-2016·2016-08-17

    Let's Do Lunch Turkey Ham & Cheese Sandwiches Recalled for Listeria Risk

    Let's Do Lunch, Inc. is recalling Integrated Food Service Turkey Ham & Cheese Sandwiches due to potential Listeria monocytogenes contamination.

    Product
    Integrated Food Service Turkey Ham & Cheese Sandwich Code #C13001/130001
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1886-2016·2016-08-17

    Let's Do Lunch Turkey Ham and Cheese Sandwiches Recalled for Listeria

    Let's Do Lunch, Inc. is recalling specific Turkey Ham & Cheese Sandwiches on Whole Grain Knot Rolls due to potential Listeria monocytogenes contamination.

    Product
    Integrated Food Service Turkey Ham & Cheese Sandwich on a Whole Grain Knot Roll Code #130008/C13008
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1914-2016·2016-08-17

    Let's Do Lunch Egg & Cheese Bagel Sandwich Recalled for Listeria

    Let's Do Lunch, Inc. is recalling Integrated Food Service Egg & Cheese Bagel Thin Sandwiches due to potential Listeria monocytogenes contamination.

    Product
    Integrated Food Service Egg & Cheese Bagel Thin Sandwich Code #C38004/380004
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1898-2016·2016-08-17

    Let's Do Lunch Recalls Beef Burger Patties for Listeria Risk

    Let's Do Lunch, Inc. is recalling Integrated Food Service All America Burger Beef Patties due to potential Listeria monocytogenes contamination.

    Product
    Integrated Food Service All America Burger Beef Patty on a Whole Grain Bun Code #470007
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1906-2016·2016-08-17

    Let's Do Lunch Recalls Chili Cheese Dogs for Listeria Risk

    Let's Do Lunch, Inc. is recalling Integrated Food Service Chili Cheese Dogs on Whole Grain Buns due to potential Listeria monocytogenes contamination.

    Product
    Integrated Food Service Chili Cheese Dog on Whole Grain Buns Code #809022
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1907-2016·2016-08-17

    Let's Do Lunch Recalls Chicken Little Sliders for Listeria Risk

    Let's Do Lunch, Inc. is recalling Integrated Food Service Chicken Little Sliders-Wrapped due to potential Listeria monocytogenes contamination.

    Product
    Integrated Food Service Chicken Little Sliders-Wrapped Code #809050
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1909-2016·2016-08-17

    Let's Do Lunch Recalls Chicken Hot Dog for Listeria Risk

    Let's Do Lunch, Inc. is recalling Integrated Food Service Chicken Hot Dog on a Whole Grain Bun due to potential Listeria monocytogenes contamination.

    Product
    Integrated Food Service Chicken Hot Dog on a Whole Grain Bun Code #941500
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1896-2016·2016-08-17

    Let's Do Lunch Recalls Chicken Patty Sandwiches for Listeria Risk

    Let's Do Lunch, Inc. is recalling Integrated Food Service Chicken Patty Sandwiches due to potential Listeria monocytogenes contamination.

    Product
    Integrated Food Service Chicken Patty Sandwich Chicken Patty on a Whole Grain Bun Code #400003
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1455-2016·2016-08-17

    Teva Recalls Albuterol Sulfate Syrup Due to Foreign Particles

    Teva North America is recalling 8,052 bottles of Albuterol Sulfate Syrup because black particles were found in the product.

    Product
    Albuterol Sulfate Syrup, 2 mg/ 5 mL, 473 mL bottle, Rx only, Manufactured in Canada by Contract Pharmaceuticals Limited, Canada, Manufactured For: Teva Pharmaceuticals USA, Sellersville, PA --- NDC 0093-0661-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1910-2016·2016-08-17

    Let's Do Lunch Recalls Chili Cheese Dog Products for Listeria Risk

    Let's Do Lunch, Inc. is recalling Integrated Food Service Chili Cheese Dog products due to potential Listeria monocytogenes contamination.

    Product
    Integrated Food Service Chili Cheese Dog Whole Grain Hot Dog Bun, Chicken Frank, Chili Sauce and Reduced Sodium Reduced Fat American Cheese Code #C95150/951500
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1889-2016·2016-08-17

    Let's Do Lunch Recalls Italian Submarine Sandwiches for Listeria Risk

    Let's Do Lunch, Inc. is recalling Integrated Food Service Italian Submarine Sandwiches due to potential Listeria monocytogenes contamination. The products were distributed nationwide.

    Product
    Integrated Food Service Italian Submarine Sandwich Code #C140004/C14004
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1877-2016·2016-08-17

    Let's Do Lunch Recalls Turkey Ham & Cheese Deli Flatz for Listeria Risk

    Let's Do Lunch, Inc. is recalling Cafe Favorites Turkey Ham & Cheese Deli Flatz due to potential Listeria monocytogenes contamination. The product was distributed nationwide in the U.S.

    Product
    Cafe Favorites Turkey Ham & Cheese Deli Flatz Code #C22148/22148
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2402-2016·2016-08-17

    Invacare Bariatric Bed Junction Boxes Recalled for Fire Risk

    Invacare Corporation is recalling 1,011 Bariatric home care beds because the junction boxes may spark, posing a fire hazard in the presence of flammable materials.

    Product
    Junction Boxes, Product Usage: The Invacare Bariatric home care bed is intended to provide a rest surface with adjustable height from floor and adjustable surface contours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2342-2016·2016-08-17

    BioMerieux Recalls NucliSENS easyMAG Magnetic Silica Reagents

    BioMerieux is recalling NucliSENS easyMAG Magnetic Silica reagents due to customer complaints about amplification performance issues.

    Product
    NucliSENS easyMAG Magnetic Silica The NucliSENS easyMAG accessory products are reagents and disposable to be used with the bioMerieux extraction systems which mention these products in their User Manuals. They enable the automated extraction (purification and concentration)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2401-2016·2016-08-17

    Invacare Bariatric Bed Foot Section Recalled for Fire Hazard

    Invacare Corporation is recalling 3,050 Bariatric Bed Foot Sections because a junction box defect may cause sparks and fire.

    Product
    Invacare¿ Foot Section for Semi & Full Electric Beds, Junction Boxes, Product Usage: The Invacare Bariatric home care bed is intended to provide a rest surface with adjustable height from floor and adjustable surface contours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V605000·2016-08-17

    Road Rescue Emergency Vehicles Recalled for Electrical Short Circuit Risk

    REV is recalling 2010-2016 Road Rescue emergency vehicles due to power control modules that may cause short circuits, risking electrical damage, loss of headlights, or fire.

    Product
    ROAD RESCUE — ROAD RESCUE SPECIALTY VEHICLE, TRANSMEDIC, ULTRAMEDIC, METROMEDIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1895-2016·2016-08-17

    Let's Do Lunch Recalls Italian Deli Flatz for Listeria Risk

    Let's Do Lunch, Inc. is recalling Cafe Favorites Italian Deli Flatz due to potential Listeria monocytogenes contamination. The product was distributed nationwide in the U.S.

    Product
    Cafe Favorites Italian Deli Flatz Code #C22548/22548
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2399-2016·2016-08-17

    Invacare Bariatric Bed Recalled for Junction Box Fire Risk

    Invacare is recalling 2,184 Bariatric Beds because a defect in the Junction Box may cause sparks, posing a fire hazard in the presence of flammable materials.

    Product
    Invacare¿ Bariatric Bed w/o mattress & rails, Junction Boxes, Product Usage: The Invacare Bariatric home care bed is intended to provide a rest surface with adjustable height from floor and adjustable surface contours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2400-2016·2016-08-17

    Invacare Bariatric Bed Recalled for Potential Fire Hazard from Junction Box Sparks

    Invacare is recalling 2,702 Bariatric Beds because the junction box may spark, posing a fire risk in the presence of flammable materials.

    Product
    Invacare¿ Bariatric Bed with mattress and rails , Junction Boxes, Product Usage: The Invacare Bariatric home care bed is intended to provide a rest surface with adjustable height from floor and adjustable surface contours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2388-2016·2016-08-17

    Edan Diagnostics Recalls EtCO2 Modules for Incorrect CO2 Readings

    Edan Diagnostics is recalling 521 EtCO2 modules used in patient monitors because they may provide incorrect CO2 readings.

    Product
    EtCO2 Module -Part Number: 02.01.210699 Monitors: iM80, iM50, M50, iM70, iM60, iM8, iM8A, iM8B Patient Monitors and iM60 Vet, iM70 Vet Veterinary Monitors EtCO2 module is an optional component of the following machines: iM80, iM50, M50, iM70, iM60 and iM8, iM8A, iM8B, iM60…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2379-2016·2016-08-17

    Merge PACS software recalled due to patient name mismatch

    Merge Healthcare is recalling PACS software versions V6.0.2.0 MR2 and earlier because patient names in the interface do not match the displayed images.

    Product
    Merge PACS software. Product was distributed under the AMICAS label, Brighton, MA, but labeling was later changed to Merge Healthcare, Hartland, WI.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2397-2016·2016-08-17

    Zimmer Biomet Recalls Zyston Transform Instrument Cases Due to Locking Defect

    Zimmer Biomet Spine, Inc. is voluntarily recalling Zyston Transform Instrument Cases and Implant Kits because the implant locking mechanism is not functioning as intended.

    Product
    Zyston¿ Transform Instrument Case. Model Number PCR8200-2101. Device labeled sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide