The Recall Desk

State

American Samoa product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40576–40600 of 73831

  • ModerateFDA (Devices)·Z-0161-2018·2017-11-29

    Zimmer Biomet Recalls ROSA Surgical Device Software

    Zimmer Biomet is recalling 29 ROSA Surgical Devices due to a software issue affecting cooperative endoscopy mode.

    Product
    ROSA Surgical Device 2.5.8 It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Guidance is based on a pre-operative plan developed with three-dimensional imaging software, and uses fiducial…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0085-2018·2017-11-29

    Lorazepam Tablets Recalled Due to Incorrect Strength Labeling

    Leading Pharma, LLC is recalling Lorazepam tablets labeled as 0.5 mg but containing 1 mg. The recall addresses a labeling error affecting 2,952 bottles nationwide.

    Product
    LORAZEPAM — LORAZEPAM (LORAZEPAM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0093-2018·2017-11-29

    West-Ward Recalls Dexamethasone Sodium Phosphate Injection Due to Impurities

    West-Ward Pharmaceuticals is recalling specific lots of Dexamethasone Sodium Phosphate Injection because of high out-of-specification results for a related compound.

    Product
    DEXAMETHASONE SODIUM PHOSPHATE — DEXAMETHASONE SODIUM PHOSPHATE (DEXAMETHASONE SODIUM PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0094-2018·2017-11-29

    West-Ward Recalls Dexamethasone Sodium Phosphate Injection Due to Impurity

    West-Ward Pharmaceuticals is recalling Dexamethasone Sodium Phosphate Injection due to high levels of a related compound impurity.

    Product
    DEXAMETHASONE SODIUM PHOSPHATE — DEXAMETHASONE SODIUM PHOSPHATE (DEXAMETHASONE SODIUM PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·17V761000·2017-11-27

    Daimler Recalls 2008-2018 Trucks for Brake Light Switch Defect

    Daimler Trucks North America is recalling 2008-2018 Freightliner and Western Star trucks because the brake light switch may fail to activate lights after hard braking, increasing crash risk.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 5700, 4700, 4900, CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0395-2018·2017-11-22

    doTERRA Recalls Slim & Sassy TrimShake for Undeclared Milk Allergen

    doTERRA is voluntarily recalling Slim & Sassy TrimShake mixes because they contain an undeclared milk allergen.

    Product
    Slim & Sassy¿ TrimShake Vanilla, SKU 35180001, 1 lb 5.9 oz, HDPE tub
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0394-2018·2017-11-22

    doTERRA Recalls Slim & Sassy TrimShake for Undeclared Milk Allergen

    doTERRA is voluntarily recalling Slim & Sassy TrimShake chocolate and vanilla mixes because they contain an undeclared milk allergen.

    Product
    Slim & Sassy¿ TrimShake Chocolate, SKU 35200001, 1 lb 5.9 oz, HDPE tub
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V753000·2017-11-22

    DRV Recalls RVs with Defective Kidde Fire Extinguishers

    DRV Suites is recalling specific recreational vehicles equipped with certain Kidde fire extinguishers that may clog, require excessive force to activate, or have nozzles that detach.

    Product
    DRV — DRV MOBILE SUITE, MOBILE SUITE ESTATES, SELECT, TRADITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0090-2018·2017-11-22

    WalkMed Infusion Pump Reservoir Bags Recalled for Fluid Leaks

    WalkMed, LLC is recalling 25,920 infusion pump reservoir bags due to reported fluid leaks at the luer connection.

    Product
    Reservoir Bag for WalkMed Infusion Pump Part Number 204820 Catalog Number IPR-86/10 65 mL and Reservoir Bag for WalkMed Infusion Pump Part Number 204821 Catalog Number IPR-150/10 150 mL The WalkMed Reservoir Bag is designed for use with the WalkMed 350VL Ambulatory pump and is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0339-2018·2017-11-22

    Aurora Dark Chocolate Cherries Recalled for Undeclared Milk

    Aurora Products is recalling Dark Chocolate Cherries in 8.5 oz cups and 11 oz tubs due to undeclared milk.

    Product
    Aurora Brand Dark Chocolate Cherries packaged in: 8.5 oz. Plastic Cup 11 oz. Square Plastic Tub
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V754000·2017-11-22

    Bison Recalls 2010 Recreational Trailers Due to Fire Extinguisher Defect

    Bison Coach is recalling 2010 Stratus, Aluma Sport, Trail Express, and Trail Hand trailers because their fire extinguishers may clog or detach, posing injury risks.

    Product
    BISON — BISON STRATUS, TRAIL HAND, ALUMA SPORT, TRAIL EXPRESS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0096-2018·2017-11-22

    Zimmer Biomet ROSA Surgical Device Recalled for Potential Force Sensor Break

    Zimmer Biomet is recalling 21 ROSA Surgical Devices due to a possible break in the Force Sensor connector. The devices were distributed to facilities in Ohio, Michigan, and Texas.

    Product
    ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled electromechanical arm. It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Guidance is based on a pre-operative plan developed…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0099-2018·2017-11-22

    Zimmer Biomet Recalls ROSA Surgical Devices Due to Observed Instability

    Zimmer Biomet is recalling 53 ROSA Surgical Devices because of observed instability. The devices are computer-controlled arms used in neurosurgery.

    Product
    ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled electromechanical arm. It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Guidance is based on a pre-operative plan…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V752000·2017-11-22

    Entegra Recalls 2010-2011 RVs Due to Fire Extinguisher Defect

    Entegra is recalling 2010-2011 Aspire, Anthem, and Cornerstone RVs because the installed fire extinguishers may clog, require excessive force to activate, or have nozzles that detach.

    Product
    ENTEGRA — ENTEGRA ASPIRE, CORNERSTONE, ANTHEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18703·2017-11-22

    Goal Zero Recalls Solar Charging Stations Due to Impact Hazard

    Goal Zero is recalling Street Charge solar powered charging stations because a weld failure could cause the top post to fall, posing an impact hazard.

    Product
    Street Charge solar powered mobile device charging stations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17E071000·2017-11-22

    Prevost Recalls Commercial Bus Driver Seats Due to Stuck Seat Belt Buckles

    Prevost is recalling specific aftermarket commercial bus driver seats because the seat belt buckle may be stuck in the locked position, preventing the seat belt from latching.

    Product
    SEAT BELTS:FRONT:BUCKLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0338-2018·2017-11-22

    Aurora Dark Chocolate Almonds Recalled for Undeclared Milk

    Aurora Products is recalling Dark Chocolate Almonds nationwide and in Bermuda because the product contains undeclared milk.

    Product
    Dark Chocolate Almonds packaged in: 4 oz. Plastic Pouch, 9 oz. Plastic Cup, 9 oz. Stand Up Plastic Pouch, 12 oz. Square Plastic Tub, 17 oz. Family Size Plastic Pouch. Aurora Brand and Store Branded Labeling Include: AG Supermarkets, Belmont Market, Boiceville Market…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V765000·2017-11-22

    KME Fire Trucks Recalled for Pressure Valve Defect

    KME is recalling 74 fire trucks because corroding rings may cause pressure relief valves to open, reducing water pressure for firefighting.

    Product
    KME — KME PREDATOR SS TANKER, PREDATOR SS PUMPER, PREDATOR SS AERIAL, COMMERCIAL PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0342-2018·2017-11-22

    Aurora Dark Chocolate Almonds Recalled for Undeclared Milk

    Aurora Products is recalling Dark Chocolate Turbinado Almonds with Sea Salt because the product contains undeclared milk. The recall affects 1,128 units distributed nationwide and in Bermuda.

    Product
    Dark Chocolate Turbinado Almonds w/ Sea Salt packaged in : 7 oz. Plastic Cup Packaged under the following: Aurora Brand and Store Branded Labeling Include: Gourmet Garage, Lee's Supermarket
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0101-2018·2017-11-22

    ICU Medical Recalls Plum 360 Infusion Systems Due to Software Malfunction

    ICU Medical is recalling 21,461 Plum 360 Infusion Systems because a software defect can prevent users from stopping the pump or restarting delivery under specific conditions.

    Product
    Plum 360 Infusion System, List number 30010.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0340-2018·2017-11-22

    Aurora Dark Chocolate Cranberries Recalled for Undeclared Milk

    Aurora Products is recalling Dark Chocolate Cranberries because the product contains undeclared milk, a major food allergen.

    Product
    Dark Chocolate Cranberries packaged in: Bulk 3.5 oz. Plastic Cup 4.75 oz. Plastic Pouch 9 oz. Plastic Cup 9 oz. Plastic Pouch 11 oz. Square Plastic Tub 18 oz. Family Size Plastic Pouch 26 oz. Plastic Tray Aurora Brand and Store Branded Labeling Include: AG…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V751000·2017-11-22

    Cruiser RV Recalls Vehicles with Defective Kidde Fire Extinguishers

    Cruiser RV is recalling specific recreational vehicles equipped with certain Kidde fire extinguishers that may clog or have nozzles detach, posing injury risks during a fire.

    Product
    CRUISER RV — CRUISER RV MPG, LIBERTY, LAND ROAMER, FUN FINDER XTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide