The Recall Desk

State

American Samoa product recalls

73,187 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
5
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 5 (20%) are Severe.

Which agencies issued them

These figures cover only the 25 recalls whose distribution notice names American Samoa specifically. The 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

14576–14600 of 73212

  • SevereCPSC·23780·2023-08-10

    Polaris RZR XP Turbo and Turbo S Off-Road Vehicles Clutch Fracture Fire Injury

    Polaris recalls about 27,300 Model Year 2021 RZR XP Turbo and RZR Turbo S recreational off-road vehicles because the clutch can fracture and eject fragments, causing fires and injuries. Owners should stop using the vehicles and contact Polaris for a free clutch replacement.

    Product
    Model Year 2021 RZR XP Turbo and RZR Turbo S Recreational Off-Road Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23256·2023-08-10

    Sensio Electric and Stovetop Pressure Cookers Recalled for Burn Hazard

    Sensio Inc. is recalling approximately 860,000 electric and stovetop pressure cookers because the lid can unlock and be removed during use, causing hot contents to splash out and burn consumers. The company has received 63 incident reports, including 61 burn injuries with some involving second and third degree burns.

    Product
    Electric and stovetop pressure cookers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V571000·2023-08-10

    Autocar Recalls 2023 Xpeditor and Legend Vehicles for Driveline Bearing Defect

    Autocar is recalling 2023 Xpeditor and Legend vehicles because the powertrain driveline center support bearing hardware may not be properly secured, which could cause the driveline to detach.

    Product
    AUTOCAR — AUTOCAR XPEDITOR, LEGEND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V572000·2023-08-10

    Moto Guzzi Recalls 2023 V100 Mandello Models for Rear Shock Absorber Defect

    Piaggio Group Americas is recalling 260 2023 Moto Guzzi V100 Mandello and Mandello Aviazione motorcycles because a missing bushing may cause the rear shock absorber to break.

    Product
    MOTO GUZZI — MOTO GUZZI V100 MANDELLO AVIAZIONE, V100 MANDELLO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V570000·2023-08-10

    Maserati Recalls 2023 MC20 Cielo for Windshield Frame Sealant Defect

    Maserati is recalling 59 2023 MC20 Cielo vehicles because missing windshield frame sealant may reduce roof strength and body structure performance in a crash.

    Product
    MASERATI — MASERATI MC20 CIELO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23257·2023-08-10

    The Children's Place Baby and Toddler Boy Jeans Recalled for Choking Hazard

    The Children's Place is recalling about 97,400 units of Baby and Toddler Boy Basic Stretch Straight Leg Jeans because metal snaps can detach, posing a choking hazard to young children. No injuries have been reported.

    Product
    Baby and Toddler Boy Basic Stretch Straight Leg Jeans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23781·2023-08-10

    Restwell Room & Board Crib Mattresses Recalled for Suffocation Hazard

    Restwell Mattress Co. is recalling about 100 Room & Board brand crib mattresses because they fail to meet federal safety standards and pose a suffocation hazard to infants. Consumers should stop using the mattresses and contact Room & Board for a refund.

    Product
    Room & Board Natural Organic Latex and Latex and Spring Crib Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V567000·2023-08-10

    2022-2023 Chevrolet Bolt EV air bag deployment defect recall

    General Motors is recalling certain 2022-2023 Chevrolet Bolt EV vehicles because the instrument panel cover may lack a required perforation, preventing proper passenger-side air bag deployment.

    Product
    CHEVROLET — CHEVROLET BOLT EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23260·2023-08-10

    Red Apple Fireworks recalled for premature explosion and burn hazards

    13131 Imports is recalling Red Apple Fireworks brand "American Glory" and "Merica AF" shell fireworks due to risk of premature explosion and burn injuries. The firm has received 72 reports of premature explosions, though no injuries have been reported.

    Product
    Fireworks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23258·2023-08-10

    Polaris, Bobcat, and Gravely Off-Road Vehicles Recalled for Fire Hazard

    Polaris Industries is recalling about 12,300 off-road vehicles and fuel system parts because a fuel leak can occur at the fuel pump outlet connector near a hot surface, posing a fire hazard. No fires or injuries have been reported to date.

    Product
    Polaris Off-Road Vehicles, Bobcat and Gravely Utility Vehicles, Fuel Pump Kits and Fuel Tank Assemblies
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V566000·2023-08-10

    2022-2023 Toyota Tundra Fuel Tube Chafing Damage Recall

    Toyota is recalling 2022-2023 Tundra and Tundra Hybrid vehicles because the plastic fuel tube may chafe against brake lines and leak fuel, creating a fire risk.

    Product
    TOYOTA — TOYOTA TUNDRA, TUNDRA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V565000·2023-08-10

    2023 Jeep Wrangler Brake Light Obstruction Recall

    Chrysler is recalling certain 2023 Jeep Wrangler vehicles because the spare tire may obstruct the center high-mount brake light, reducing visibility to other drivers and increasing crash risk.

    Product
    JEEP — JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V564000·2023-08-10

    Isuzu Recalls 2023-2024 NPR and Chevrolet LCF Trucks for Electrical Defect

    Isuzu is recalling 19,479 trucks because a wire seal defect may allow water intrusion, causing fuse corrosion and potential loss of engine power.

    Product
    ISUZU — ISUZU CHEVROLET LCF 4500HG, CHEVROLET LCF 5500XG, N-SERIES, CHEVROLET LCF 3500HG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·23259·2023-08-10

    Saxco International Recalls Glass Carboys Due to Laceration Hazard

    Saxco International is recalling about 8,370 glass carboys because the glass can break due to improper cooling processes, posing a laceration hazard. The firm has received 30 reports of incidents of glass breaking, though no injuries have been reported.

    Product
    Carboys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23255·2023-08-10

    Target Recalls 2.2 Million Threshold Glass Jar Candles for Laceration and Burn Hazards

    Target is recalling about 2.2 million Threshold Glass Jar Candles because the glass jars can crack or break during use, posing laceration and burn hazards. Target received 19 reports of jars breaking or cracking, resulting in one minor injury.

    Product
    Threshold Glass Jar Candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2281-2023·2023-08-09

    Impella RP Flex cardiac pump recalled for thrombus formation risk

    The Impella RP Flex cardiac pump has been recalled due to a higher-than-expected rate of blood clot formation. Blood clots may reduce cardiac support or cause hemolysis.

    Product
    Impella RP Flex with SmartAssist intracardiac microaxial blood pump, Product Number 1000323
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1081-2023·2023-08-09

    Prescription Birth Control Tablets Recalled for Failed Stability Testing

    Lupin Pharmaceuticals is recalling TYDEMY birth control tablets due to failed stability testing. Consumers should contact their healthcare provider.

    Product
    TYDEMY — TYDEMY (DROSPIRENONE, ETHINYL ESTRADIOL AND LEVOMEFOLATE CALCIUM AND LEVOMEFOLATE CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1021-2023·2023-08-09

    Cardioplegia Solution Recalled Due to Sterility Assurance Deficiency

    Central Admixture Pharmacy Services recalls Cardioplegia Solution (Lot 36-253947) due to lack of sterility assurance and insufficient decontamination validation. Healthcare facilities should discontinue use and contact the manufacturer.

    Product
    CARDIOPLEGIA SOLUTION, 25 mEq K, SUTTER CARDIOPLEGIA, IV Bag, Total Volume = 572.64 mL, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0217-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1051-2023·2023-08-09

    Fentanyl Injectable Recalled Due to Lack of Sterility Assurance

    Central Admixture Pharmacy Services is recalling fentanyl injections because sterilization procedures were not properly validated, raising infection risks from potential contamination.

    Product
    fentaNYL, 5000 mcg/100 mL, (50 mcg/mL), 100 mL Bag, Rx only, Central Admixture Pharmacy Services, Inc., 7935 Dunbrook Road, Suite C, San Diego, CA 92126, NDC: 71286-2003-5
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1009-2023·2023-08-09

    Neonatal TPN starter bags recalled for lack of sterility assurance

    Central Admixture Pharmacy Services is recalling 244 neonatal TPN IV bags due to lack of assurance that the sterility process was validated. The manufacturer lacked adequate validation data for their decontamination cycles.

    Product
    Neonatal TPN Starter Bag, Amino Acids (trophamine) 3.5%/Dextrose 10% with HEPARIN, IV Bag, total volume = 250mL, Rx only, Central Admixture Pharmacy Services, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-0431-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2336-2023·2023-08-09

    Medline Procedural Kits Recalled Due to Sterility Specification Concerns

    Medline Industries is recalling 211 custom procedural kits (egg retrieval, fetal surgery, TVT packs) worldwide because the sterile ultrasound gel component may not meet sterility specifications. Kits were distributed between April 2020 and April 2023.

    Product
    Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound Gel. Labeled as the following: a. EGG RETRIEVAL PACK, Model Number: DYNJ66291B; b. FETAL SURGERY CDS-LF, Model Number: CDS840214P; c. TVT PACK SMGH-LF, Model Number: DYNJ41913C;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2264-2023·2023-08-09

    Olympus SPiN Drive Forceps Recalled for EM Sensor Malfunction

    Olympus SPiN Drive Forceps are being recalled due to an electromagnetic sensor malfunction that disables navigation functionality during endobronchial procedures, potentially causing procedural delays. No injuries reported.

    Product
    Always-On Tip Tracked Instruments (SPiN Drive instruments) Forceps, 1.8mm OD, Serrated Cup-Intended for use in clinical interventions and for anatomical structures where computed tomography and/or endoscopic brINS-0362onchoscopy are currently used for visualizing Model…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0986-2023·2023-08-09

    FDA Recalls OxyTOCIN IV Bags Over Sterility Assurance Defect

    FDA recalls 130,250 bags of oxyTOCIN IV solution from CAPS, Inc., distributed nationwide, due to lack of validated sterilization procedures. No illnesses reported.

    Product
    oxyTOCIN 30 units added to 0.9% sodium chloride 500 mL, IV Bag, Rx only, This drug was repacked by CAPS, Inc., 2200 South 43rd Avenue, Pheonix, AZ 85043, NDC: 72196-6044-1
    Category
    Drug
    Distribution
    Distributed nationwide