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.

49126–49150 of 73852

  • SevereNHTSA·16V225000·2016-04-19

    Forest River Recalls 2016 Glaval Buses Due to Seat Separation Risk

    Forest River is recalling 2016 Glaval Entourage and Universal buses because seats may separate from the base frame due to bolt failure, increasing injury risk in a crash.

    Product
    GLAVAL BUS — GLAVAL BUS ENTOURAGE, UNIVERSAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V223000·2016-04-19

    New Flyer Transit Buses Recalled for Rear Door Software Defect

    New Flyer is recalling specific transit buses because a software defect may cause the rear door to open unexpectedly while the bus is moving, increasing injury risk.

    Product
    NEW FLYER — NEW FLYER XN40, XN60, C40LFR, XN35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16147·2016-04-19

    Flying Tiger Copenhagen Recalls Wooden Toys Due to Choking Hazard

    Flying Tiger Copenhagen is recalling wooden blocks and giraffe toys because parts can detach and pose a choking hazard to young children.

    Product
    Wooden Toy Blocks and Giraffes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16145·2016-04-15

    Miniland Recalls Moogy Plush Toys Due to Choking Hazard

    Miniland Educational is recalling Moogy plush toys because buttons can detach, posing a choking hazard to young children.

    Product
    Moogy plush toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V215000·2016-04-14

    Toyota Recalls 2016 Camry and Avalon for Air Bag Calibration Issues

    Toyota is recalling 58,515 model year 2016 Camry and Avalon vehicles because the occupant classification system may be improperly calibrated, potentially preventing front passenger air bags from deploying.

    Product
    TOYOTA — TOYOTA CAMRY, AVALON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E035000·2016-04-14

    Steve Johnson Induction Solutions Recalls Nitrous Oxide Solenoid Valves

    Steve Johnson Induction Solutions is recalling specific nitrous oxide solenoid valves because end stops may break under pressure, posing an injury risk.

    Product
    FUEL SYSTEM, OTHER:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V217000·2016-04-14

    Glaval Bus Transit Models Recalled for Emergency Exit Label Placement

    Forest River is recalling 2008-2016 Glaval Bus transit models because rear emergency exit labels are not placed within 16 centimeters of release mechanisms, potentially hindering quick escape.

    Product
    GLAVAL BUS — GLAVAL BUS TITAN II, APOLLO, TITAN II LOW FLOOR, TITAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16143·2016-04-14

    Fisher-Price Recalls Infant Cradle Swings Due to Fall Hazard

    Fisher-Price is recalling about 34,000 infant cradle swings because the seat peg may not be fully engaged, allowing the seat to fall unexpectedly.

    Product
    Cradle 'n Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1275-2016·2016-04-13

    FDA Recalls Guardian II Hemostasis Valves Due to Air Embolism Risk

    Vascular Solutions is recalling Guardian II Hemostasis Valves because the low-pressure seal may fail, potentially allowing air into the device and causing an air embolism.

    Product
    Guardian II Hemostasis Valve, models 8210 and 8211. The following models are only available Outside the US: FH101, FH101-T, FH101-25, and FH101-50. Product Usage: The Guardian hemostasis valves are designed to be used as conduits when interventional devices with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0803-2016·2016-04-13

    Meditech Formula 4 Injection Recalled for Sterility Assurance Issues

    Meditech Laboratories is recalling Formula 4 Injection vials due to incomplete data regarding production sterility.

    Product
    Formula 4 (Papaverine 18 mg, Phentolamine 2 mg, Atropine 0.2 mg/mL) Injection, 5 mL vials, Rx only, Meditech Laboratories, Inc., 3200 Polaris Ave., Suite 27, Las Vegas, NV 89102. .
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0808-2016·2016-04-13

    Meditech Formula 2 Vials Recalled Due to Expired Active Ingredient

    Meditech Laboratories is recalling Formula 2 vials because an active ingredient expired before the labeled Beyond Use Date.

    Product
    Formula 2 (Papaverine 9 mg, Phentolamine 1 mg, Atropine 0.1 mg, PGE 10 mcg/mL), 5 mL vials, Meditech Laboratories, Inc., 3200 Polaris Ave., Suite 27, Las Vegas, NV 89102.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1039-2016·2016-04-13

    NutraKey Recalls VPro Raw Plant Protein Due to Undeclared Soy

    NutraKey, Inc. is recalling VPro Raw Plant Protein, Chocolate, because it contains undeclared soy. The recall covers 17,730 units distributed nationwide.

    Product
    VPro Raw Plant Protein, Chocolate. Packaged in a plastic bottle with green, white, and black adhesive label. Packaged in 1 lb (15 serving) and 2 lb (30 serving).
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1002-2016·2016-04-13

    Whole Foods Market Recalls Maytag Blue Cheese for Listeria Risk

    Whole Foods Market is recalling Maytag Blue Cheese products due to possible contamination with Listeria monocytogenes.

    Product
    Whole Foods Market Maytag Blue Cheese, Maytag Blue Raw Milk, Maytag Iowa Blue Cheese cut and wrapped in clear plastic wrap, Dist. by Whole Foods Market 550 Bowie Street Austin, TX 78703, PLU: 0293308
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0816-2016·2016-04-13

    Actavis Recalls Amphetamine Tablets Due to Impurity Failures

    Actavis is recalling specific lots of amphetamine tablets because they failed impurity specifications. Consumers should stop using the product and contact their pharmacist.

    Product
    Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 5 mg, 100 ct. bottle, Rx Only. Manufactured by: Actavis Elizabeth LLC, Elmora Avenue, Elizabeth, NJ 07207. Distributed by: Actavis, Inc., 80 Columbia Road, Bldg B…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1272-2016·2016-04-13

    Focus Diagnostics Recalls Simplexa HSV 1&2 Direct Amplification Discs

    Focus Diagnostics is recalling Simplexa HSV 1&2 Direct Amplification Discs because they may cause false negative or positive results and error codes.

    Product
    Simplexa HSV 1&2 Direct (MOL2150) with Direct Amplification Disc (MOL1451, MOL1452, MOL1455) Model Number: MOL2150, MOL1451, MOL1452, MOL1455
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1040-2016·2016-04-13

    NutraKey Recalls VPro Raw Plant Protein for Undeclared Soy

    NutraKey, Inc. is voluntarily recalling VPro Raw Plant Protein, Vanilla, due to undeclared soy. The product was distributed nationwide.

    Product
    VPro Raw Plant Protein, Vanilla. Packaged in a plastic bottle with green, white, and black adhesive label. Packaged in 1 lb (15 serving) and 2 lb (30 serving).
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1274-2016·2016-04-13

    Focus Diagnostics Recalls Simplexa Group A Strep Direct Amplification Discs

    Focus Diagnostics is recalling Simplexa Group A Strep Direct Amplification Discs because they may cause false test results or error codes.

    Product
    Simplexa Group A Strep Direct (MOL2850) with Direct Amplification Disc (MOL1451, MOL1452, MOL1455) Model Number: MOL2850, MOL1451, MOL1452, MOL1455
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1327-2016·2016-04-13

    Synthes Recalls Titanium Low Profile Neuro Screws Due to Thread Defect

    Synthes (USA) Products LLC is recalling specific lots of Titanium Low Profile Neuro Screws because the thread height is undersized, potentially compromising the device's structural integrity.

    Product
    Titanium Low Profile Neuro Screw, Self Drilling, 3mm, part numbers: 400.833, 400.833E Product Usage: The Low Profile Neuro Plating System is intended for use in selective trauma of the midface and craniofacial skeleton; craniofacial surgery; reconstructive procedures; and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V211000·2016-04-13

    Mercedes-Benz Recalls 2016 SLK300 Vehicles Due to Ignition Wiring Defect

    Mercedes-Benz is recalling 2016 SLK300 vehicles because a backup power supply for the ignition switch may not be properly connected, creating a risk of the vehicle rolling.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SLK300
    Category
    Vehicle
    Distribution
    Distributed nationwide