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.

46776–46800 of 73849

  • ModerateFDA (Drugs)·D-1478-2016·2016-09-07

    Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels

    Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.

    Product
    CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-48241-1, Shade 06 (D-G)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1473-2016·2016-09-07

    Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels

    Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.

    Product
    CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47476-8, Shade 01 (VF-N)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1476-2016·2016-09-07

    Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels

    Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.

    Product
    CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47479-9, Shade 04 (M-N)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V640000·2016-09-06

    Acura Recalls 2015 TLX Vehicles for Transmission Wire Harness Defect

    Honda is recalling 2015 Acura TLX vehicles because transmission wire harness connections may have insufficient crimps, causing the vehicle to unexpectedly shift to neutral and increasing crash risk.

    Product
    ACURA — ACURA TLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V641000·2016-09-06

    Audi Recalls 2017 Q7 Vehicles for Third-Row Seat Back Defect

    Volkswagen Group of America is recalling 2017 Audi Q7 vehicles because the third-row seat back may move forward in a crash, increasing injury risk.

    Product
    AUDI — AUDI Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V643000·2016-09-06

    Ford Recalls Multiple Models Due to Door Latch Defect

    Ford is recalling specific 2012-2016 vehicles because door latches may break, allowing doors to open while driving.

    Product
    FORD — FORD, LINCOLN ESCAPE, TRANSIT CONNECT, MKC, MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V644000·2016-09-06

    Mazda Recalls Vehicles Due to Corroded Lift Gate Support Struts

    Mazda is recalling specific 2010-2016 models because lift gate support struts may corrode and break, causing the gate to drop unexpectedly and injure users.

    Product
    MAZDA — MAZDA MAZDASPEED3, MAZDA3, MAZDA5, CX-5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V642000·2016-09-06

    Audi Recalls Vehicles Due to Inoperative Side Marker Lights

    Volkswagen Group of America is recalling certain Audi models because software may cause side marker lights to fail, reducing visibility at night.

    Product
    AUDI — AUDI A4 ALLROAD, TT ROADSTER, A3 CABRIOLET, Q3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V636000·2016-09-02

    Nissan Recalls Maxima and Murano Models Due to Brake Fluid Leak Fire Risk

    Nissan is recalling certain 2015-2017 Maxima and Murano vehicles because brake fluid may leak onto an electrical circuit board, increasing the risk of a fire.

    Product
    NISSAN — NISSAN MAXIMA, MURANO HYBRID, MURANO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V638000·2016-09-02

    Tiffin Recalls 2017 Allegro Bus Motorhomes Due to Mirror Defect

    Tiffin is recalling 2017 Allegro Bus motorhomes because the passenger side mirror may move while driving, reducing visibility and increasing crash risk.

    Product
    TIFFIN — TIFFIN ALLEGRO BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16772·2016-09-02

    John Deere Recalls Backhoe Attachments Due to Crushing Hazard

    John Deere is recalling about 50 model 485A backhoe attachments because mounting hardware could loosen, causing the frame to rotate and crush the operator.

    Product
    Backhoe attachments for compact utility tractors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V635000·2016-09-01

    Kaufman Recalls 2015-2016 Mini Car Haulers Due to Suspension Defect

    Kaufman Trailers is recalling 285 model year 2015-2016 Mini 5-Car Haulers because a suspension spring eye may break, allowing the axle to slide and increasing crash risk.

    Product
    KAUFMAN — KAUFMAN MINI CAR HAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16257·2016-09-01

    Polaris Recalls RZR XP Turbo Vehicles Due to Fire and Burn Hazards

    Polaris is recalling approximately 13,000 RZR XP Turbo recreational off-highway vehicles because engine overheating and loose drain tubes can cause fires and severe burn injuries.

    Product
    Recreational Off-Highway Vehicles (ROVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16T013000·2016-09-01

    Goodyear Recalls G399A LHS Tires Due to Tread Separation Risk

    Goodyear is recalling specific G399A LHS tires due to a manufacturing defect that may cause tread separation, increasing the risk of a crash.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16256·2016-09-01

    SAHN Designs Recalls Bicycle Helmets Due to Head Injury Risk

    SAHN Designs is recalling SAHN Classic SH523 bicycle helmets because they do not meet federal impact safety standards, posing a risk of head injury.

    Product
    SAHN Classic bicycle helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2358-2016·2016-08-31

    Alere INRatio2 PT/INR Home Monitoring System Recalled for Inaccurate INR Results

    Alere San Diego is voluntarily recalling INRatio2 PT/INR Home Monitoring Systems because they may display inaccurate INR results compared to central laboratory tests.

    Product
    Alere INRatio2 PT/INR Home Monitoring System Model Number: 0200432, 0200433 Product Usage: Alere INRatio 2 PT/INR Home Monitoring System: The Alere INRatio 2 PT/INR Home Monitoring System, consisting of the INRatio 2 Home Monitor and INRatio PT/INR test strip, is used for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2614-2016·2016-08-31

    Cook Inc. Recalls Slip-Cath Beacon Tip Catheters Due to Tip Fracture

    Cook Inc. is recalling Slip-Cath Beacon Tip Catheters because polymer degradation can cause the tip to fracture or separate, potentially leading to device fragments in the body.

    Product
    Slip-Cath Beacon Tip Catheter Catheter, Intravascular, Diagnostic The catheters are intended for use in angiographic procedures by physicians trained and experienced in angiographic techniques.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2651-2016·2016-08-31

    Medtronic Evera ICDs Recalled for Rapid Battery Depletion Risk

    Medtronic is recalling 78 Evera ICDs and Viva CRT-Ds due to a circuit defect causing rapid battery depletion. Seven confirmed failures have resulted in complications like shortness of breath.

    Product
    Medtronic, Evera Implantable Cardioverter Defibrillators: Product Model EVERA XT DDBB1D1, DDBB1D4, DDBB2D1, DDBB2D4, DVBB2D4, DVBB1D1. EVERA S DDBC3D1, DDBC3D4 Product Usage: The Medtronic Evera DR dual chamber and Evera VR single chamber, implantable…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2356-2016·2016-08-31

    Alere INRatio PT Monitoring Systems Recalled for Inaccurate INR Results

    Alere San Diego is voluntarily recalling INRatio PT Monitoring Systems because they may show lower INR results than central laboratory tests, potentially affecting warfarin therapy.

    Product
    Alere INRatio Replacement Monitor Model Number: 0100137 Usage: The INRatio 2 PT Monitoring system is used for the quantitative measurement of Prothrombin Time (PT) in fresh, capillary whole blood. The INRatio 2 PT Monitoring system is intended for use outside the body (in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1468-2016·2016-08-31

    Mylan Amlodipine Tablets Recalled for CGMP Deviations

    Mylan Institutional is recalling Amlodipine Besylate Tablets 10 mg because they were produced with active ingredients not manufactured according to Good Manufacturing Practices.

    Product
    Amlodipine Besylate Tablets, USP, 10 mg*, packaged in a) 100-count (10 x 10) unit dose blisters per carton, NDC 51079-452-20; b) 300-count (10 x 30) unit dose blisters per carton, NDC 51079-452-56; and c) 25-count (25 x 1) Robot-Rx Ready Packages in a carton, NDC 51079-452-19…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2623-2016·2016-08-31

    Cook Inc. Recalls White Lumax Guiding Coaxial Catheters Due to Tip Fracture

    Cook Inc. is recalling 3,425 White Lumax Guiding Coaxial Catheters worldwide due to polymer degradation that can cause the catheter tip to fracture or separate.

    Product
    White Lumax Guiding Coaxial Catheter Catheter, Percutaneous Intended for the delivery of angioplasty balloons and other types of interventional devices.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2616-2016·2016-08-31

    Cook Inc. Recalls Haskal Transjugular Intrahepatic Portal Access Sets

    Cook Inc. is recalling Haskal Transjugular Intrahepatic Portal Access Sets due to polymer degradation that can cause catheter tip fracture and separation.

    Product
    Haskal Transjugular Intrahepatic Portal Access Set Introducer, catheter Intended for transjugular liver access in diagnostic and interventional procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1466-2016·2016-08-31

    Mylan Amlodipine Tablets Recalled for CGMP Deviations

    Mylan Institutional, Inc. is recalling Amlodipine Besylate Tablets because they were not manufactured according to Good Manufacturing Practices.

    Product
    Amlodipine Besylate Tablets, USP, 2.5 mg*, packaged in a)100-count (10 x 10) unit dose blisters per carton, NDC 51079-450-20 and b) 30-count tablets per dosage card in a carton, NDC 51079-450-63, Rx only, Manufactured by: Mylan Pharmaceuticals Inc., Morgantown, WV 26505…
    Category
    Drug
    Distribution
    Distributed nationwide