The Recall Desk

State

American Samoa product recalls

73,597 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 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29551–29575 of 73622

  • LowFDA (Devices)·Z-1470-2020·2020-03-18

    Integra NeuraGen Nerve Guide Recalled for Quality Control Error

    Integra LifeSciences is recalling 55 units of NeuraGen Nerve Guides because nonconforming product was mistakenly released for commercial use.

    Product
    NeuraGen Nerve Guide, 7mm diameter, 2cm length; Part number PNG72 - Product Usage: NeuraGen nerve guide is indicated for the repair of peripheral nerve discontinuities where gap closure can be achieved by flexion of the extremity.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1055-2020·2020-03-18

    Lupin Recalls Bekyree Tablets Due to Content Uniformity Failures

    Lupin Pharmaceuticals is recalling specific lots of Bekyree oral contraceptives because they failed content and blend uniformity tests.

    Product
    Bekyree (desogestrel and ethinyl estradiol tablets USP, 0.15 mg/0.02 mg and ethinyl estradiol tablets USP, 0.01 mg), packaged in 1 Wallet of 28 Tablets (NDC 68180-879-11), 3 Wallets of 28 Tablets Each per carton (NDC 68180-879-13), Rx Only, Distributed by: Lupin Pharmaceuticals…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·20090·2020-03-17

    Honda Recalls Portable Generators Due to Fire and Burn Hazards

    American Honda is recalling about 340,000 portable generators because the inverter assembly can short-circuit in salt water, causing smoke or fire.

    Product
    Honda EB2200i, EU2200i, EU2200i Companion and EU2200i Camo Portable Generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V148000·2020-03-17

    2020 Thor Sequence motorhomes recalled for transmission shifter cable separation

    Thor Motor Coach is recalling 2020 SEQUENCE motorhomes because the transmission shifter cable may separate from the transmission, potentially causing unintended vehicle movement and increased crash risk.

    Product
    THOR — THOR, THOR MOTOR COACH SEQUENCE, TELLARO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V150000·2020-03-17

    Triumph Recalls Trophy Motorcycles Due to Brake Hose Routing Defect

    Triumph is recalling 2013-2017 Trophy SE A1 motorcycles because improper brake hose routing may damage ignition wiring, causing engine stalls or lighting loss.

    Product
    TRIUMPH — TRIUMPH TROPHY, TROPHY SE A1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V149000·2020-03-16

    Audi Recalls Q7 and Q8 Models Due to Steering Shaft Bolt Issue

    Volkswagen Group of America is recalling 2017-2019 Audi Q7 and 2019 Q8 vehicles because a steering shaft bolt may loosen, potentially causing a loss of steering control.

    Product
    AUDI — AUDI Q7, Q8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V147000·2020-03-16

    Eldorado World Trans Recalled for Improperly Secured Seat Belts

    Eldorado National-Kansas is recalling 2017-2019 World Trans vehicles because seat belts may not be properly secured to the side wall, increasing injury risk in a crash.

    Product
    ELDORADO — ELDORADO WORLD TRANS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20T006000·2020-03-13

    Tornel Deportiva Tires Recalled for Tread Separation Risk

    Tornel is recalling specific Deportiva tires where adhesive failure may cause tread separation, increasing the risk of vehicle control loss and crashes.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V145000·2020-03-13

    Nissan Recalls 2020 Infiniti Q60 Vehicles for Rear Seat Belt Defect

    Nissan is recalling 2020 Infiniti Q60 vehicles because the rear seat belt locking mechanism may fail to lock properly, increasing injury risk in crashes.

    Product
    INFINITI — INFINITI Q60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V142000·2020-03-12

    GM Recalls 2020 Silverado and Sierra Trucks for Hood Latch Defect

    General Motors is recalling 2020 Chevrolet Silverado and GMC Sierra trucks because improperly heat-treated hood-latch wires may fracture, allowing the hood to open while driving.

    Product
    GMC — GMC, CHEVROLET SIERRA 3500, SILVERADO 2500, SILVERADO 3500, SIERRA 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V146000·2020-03-12

    BMW Recalls 2019-2020 Motorcycles Due to Flashing Brake Light Defect

    BMW is recalling specific 2019-2020 motorcycles because the brake light may flash instead of staying steady during emergency braking, which can confuse other drivers.

    Product
    BMW — BMW S1000 R, F 850 GS ADVENTURE, F 900 R, R NINE T SCRAMBLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20089·2020-03-12

    Yamaha Recalls Line 6 Relay G10 Wireless Guitar Systems for Fire Hazards

    Yamaha is recalling Line 6 Relay G10 wireless guitar systems because the lithium-ion battery can overheat and the cover can separate, posing fire and injury risks.

    Product
    Line 6 Relay G10 Digital Wireless Guitar Systems and USB Charging Cables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20088·2020-03-12

    Kichler Recalls 52-inch LED Ceiling Fans Due to Blade Detachment Hazard

    Kichler Lighting is recalling 52-inch LED ceiling fans because the arms holding the blades can detach, posing an injury risk. No injuries have been reported.

    Product
    Kichler 52-inch LED Indoor Ceiling fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0968-2020·2020-03-11

    Axia Pharmaceutical Recalls Methylprednisolone Acetate/Bupivacaine Injectable Suspension

    Axia Pharmaceutical is recalling Methylprednisolone Acetate/Bupivacaine Injectable Suspension due to a lack of assurance of sterility.

    Product
    Methylprednisolone Acetate/Bupivacaine Hydrochloride Injectable Suspension, METHYLPRED ACETATE/BUPIV [10ML] CMC 40MG/5MG/ML INJ SUSP, For IM, IA Use, Shake Well, 10 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0991-2020·2020-03-11

    Axia Pharmaceutical Recalls Triamcinolone Diacetate Injectable Suspension Due to Sterility Concerns

    Axia Pharmaceutical is recalling specific lots of Triamcinolone Diacetate Injectable Suspension because the product lacks assurance of sterility.

    Product
    Triamcinolone Diacetate Injectable Suspension, TRIAMCINOLONE DIACETATE [10ML] CMC 80 MG/ML INJ SUSP, For IM, IA, IT Use, 10 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0634-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0976-2020·2020-03-11

    Axia Pharmaceutical Recalls Mitomycin-C Irrigation Solution Due to Sterility Concerns

    Axia Pharmaceutical is recalling specific lots of Mitomycin-C Irrigation Solution because the FDA cannot assure the sterility of the product.

    Product
    Mitomycin-C (PF) Irrigation Solution, MITOMYCIN-C (PF) 0.5 MG/ML PF SYRINGE, For Intravesicular Use, Freeze, Cytoxic Agent, Preservative Free, Protect From Light, 80 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0941-2020·2020-03-11

    Axia Pharmaceutical Recalls B-Complex 110 Injectable Due to Sterility Concerns

    Axia Pharmaceutical is recalling B-Complex 110 Injectable vials due to a lack of assurance of sterility. The affected lots were distributed nationwide and in several international locations.

    Product
    B-COMPLEX 110 INJECTABLE, For IV, IM, SC Use, Refrigerate, 30 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0212-3
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0951-2020·2020-03-11

    Axia Pharmaceutical Recalls Dexamethasone Injectable Suspension Due to Sterility Concerns

    Axia Pharmaceutical is recalling Dexamethasone (LA) Injectable Suspension because the product lacks assurance of sterility. The recall covers specific lots distributed in the U.S., Puerto Rico, Barbados, and the Dominican Republic.

    Product
    Dexamethasone (LA) Injectable Suspension, DEXAMETHASONE LA [10ML] 16MG INJ SUSP, For IM, IA Use, Shake Well, 10 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0630-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0980-2020·2020-03-11

    Axia Pharmaceutical Recalls Pyridoxine Hydrochloride Injection Due to Sterility Concerns

    Fusion IV Pharmaceuticals is recalling specific lots of Pyridoxine Hydrochloride Injection due to a lack of assurance of sterility. The product was distributed nationwide and in several Caribbean territories.

    Product
    Pyridoxine Hydrochloride Injection, PYRIDOXINE HCL 100 MG/ML INJECTABLE, For IV, IM Use, 30 mL Multi-dose Vial, Rx only, Axia Pharmaceutical 1990 Westwood Blvd. Ste 135, Los Angeles, CA 90025; NDC 71283-0216-3
    Category
    Drug
    Distribution
    Distributed nationwide