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.

14201–14225 of 73212

  • ModerateFDA (Devices)·Z-2590-2023·2023-09-27

    Arrow ErgoPack PICC Catheters Recalled for Incorrect Product Labeling

    Arrow International is recalling 190 units of Arrow ErgoPack One-Lumen PICC catheters (Lot 13F22J0617) because the product code and product name were incorrectly printed on the kit packaging. The units were distributed nationwide.

    Product
    Arrow ErgoPack Pressure Injectable One-Lumen PICC, REF CDC-05541-HPK1A; catheter, intravascular
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1168-2023·2023-09-27

    ChloraPrep One-Step Topical Applicators Recalled for Unsupported Shelf-Life Claims

    BD ChloraPrep One-Step topical applicators are recalled because the 36-month shelf life is not supported by stability data; the product may develop fungal contamination beyond 12 months.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1172-2023·2023-09-27

    Cequa cyclosporine ophthalmic solution recalled nationwide for subpotency

    Sun Pharmaceutical is recalling Cequa (cyclosporine) ophthalmic solution because certain lots contain less active ingredient than specified. Contact your doctor if using an affected product.

    Product
    CEQUA — CEQUA (CYCLOSPORINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2591-2023·2023-09-27

    Arrow ErgoPack PICC catheter kits recalled for incorrect product labeling

    Arrow International recalled 177 ErgoPack PICC catheter kits because the product code and name were incorrectly listed on the packaging. No illnesses or injuries reported.

    Product
    Arrow ErgoPack, Pressure Injectable Two-Lumen PICC pre-loaded with Arrow VPS Stylet, REF CDC-35552-VPS; Catheter: Percutaneous, implanted, long-term intravascular catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V652000·2023-09-25

    Kia Recalls Multiple Models Due to Electrical Short Fire Risk

    Kia is recalling 1.7 million vehicles because an electrical short in the brake control unit may cause an engine compartment fire.

    Product
    KIA — KIA SOUL, OPTIMA HYBRID, SPORTAGE, SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V651000·2023-09-22

    Hyundai Recalls Multiple Models Due to ABS Module Fire Risk

    Hyundai is recalling over 1.6 million vehicles because a leaking ABS module may cause an engine compartment fire. Owners should park outside until the repair is complete.

    Product
    HYUNDAI — HYUNDAI ELANTRA, AZERA, SANTA FE, GENESIS COUPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V649000·2023-09-22

    2023 Kia Forte Right Front Control Arm Defect Recall

    Kia is recalling 2023 Forte vehicles due to improper welds on the right front lower control arm, which may fail and cause loss of steering control. Affected owners should not drive the vehicle until repaired.

    Product
    KIA — KIA FORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V648000·2023-09-22

    2024 East to West RV Recall: Detachable Rear Ladder Poses Injury Risk

    Forest River is recalling certain 2024 East to West Blackthorn and Tandara fifth wheels. The rear ladder may detach due to improper anchoring, creating a potential injury risk.

    Product
    EAST TO WEST — EAST TO WEST BLACKTHORN, TANDARA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V650000·2023-09-22

    2024 Hyundai Kona Seat Belt Retractor Malfunction Recall

    Hyundai is recalling certain 2024 Kona vehicles because the rear seat belt retractors may not function properly. A defective seat belt could fail to restrain occupants in a crash, increasing injury risk.

    Product
    HYUNDAI — HYUNDAI KONA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·23290·2023-09-21

    HONEY JOY Infant Swings Recalled for Suffocation Hazard

    HONEY JOY infant swings are recalled due to a suffocation hazard. The product violates federal safety standards because it has an incline angle greater than 10 degrees and was marketed for infant sleep, and infant fatalities have been reported in similar inclined sleepers.

    Product
    HONEY JOY Infant Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23294·2023-09-21

    Shimano 11-Speed Road Cranksets Recalled for Crash Hazard

    Shimano is recalling about 680,000 bonded 11-speed road cranksets because the crank parts can separate and break, posing a crash hazard. Six injuries including bone fractures have been reported.

    Product
    11-Speed Bonded Hollowtech II Road Cranksets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V647000·2023-09-21

    2023 Subaru Driveshaft Center Support Bolts May Loosen

    Subaru is recalling certain 2023 Ascent, Legacy, Impreza, and Outback vehicles because center support bolts for the driveshaft may loosen, potentially causing the driveshaft to disconnect and increasing crash risk. Dealers will clean and replace the bolts at no charge.

    Product
    SUBARU — SUBARU OUTBACK, ASCENT, LEGACY, IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23293·2023-09-21

    H&M Men's Clasp Beaded Bracelets Recalled for High Lead Content

    H&M is recalling about 12,290 men's clasp beaded bracelets because the clasp contains lead levels exceeding the federal ban. Lead is toxic if ingested by young children and can cause adverse health effects.

    Product
    Men's clasp beaded bracelets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23291·2023-09-21

    DR Power Chipper Shredders Recalled Due to Laceration Hazard

    DR Power Chipper Shredders are being recalled because metal pieces can come loose and be ejected, or the hopper can detach, both creating laceration hazards. The firm has received 79 reports of parts coming loose and 3 reports of hopper detachment, with a total of 3 reported injuries.

    Product
    DR Power Chipper Shredders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23793·2023-09-21

    Novaform ComfortGrande and DreamAway Mattresses Recalled for Mold Contamination

    FXI recalls about 48,000 Novaform mattresses from Costco due to mold contamination from water exposure during manufacturing. The mold poses a health risk to people with compromised immune systems or mold allergies. No injuries have been reported.

    Product
    Novaform ComfortGrande 14-inch and Novaform DreamAway 8-inch Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23292·2023-09-21

    Rainbow Road Series Board Books Recall: Detachable Plastic Rings Choking Hazard

    Make Believe Ideas recalls seven Rainbow Road Series board books because plastic binding rings can detach, posing a choking hazard to young children. About 260,000 units were sold nationwide from March 2022 through August 2023.

    Product
    Rainbow Road Series Board Books
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2509-2023·2023-09-20

    Abbott Proclaim DRG Implantable Pulse Generators cannot exit MRI mode

    Abbott Medical is recalling approximately 17,394 Proclaim DRG Implantable Pulse Generators worldwide due to reports that patients cannot exit MRI mode on affected devices. This malfunction may prevent normal device operation when mode-switching is needed.

    Product
    Proclaim DRG Implantable Pulse Generator REF 3664 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It is powered by a hermetically sealed battery…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2510-2023·2023-09-20

    Abbott Infinity 5 Implantable Pulse Generator Patients Unable to Exit MRI Mode

    Some Abbott Infinity 5 implantable pulse generator patients report being unable to exit MRI mode on their devices. This Class I recall affects 5,932 devices distributed globally.

    Product
    Infinity 5 Implantable Pulse Generator REF 6660 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It is powered by a hermetically sealed battery…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2514-2023·2023-09-20

    FDA Recalls Medline Hudson RCI Addipak Inhalation Solution for Sterility Failure

    Medline Industries is recalling HUDSON RCI Addipak 5mL sterile saline inhalation solution due to sterility failure. Approximately 18,000 units were distributed nationwide; the product was intended for scrap but was inadvertently shipped to customers.

    Product
    HUDSON RCI Addipak, UNIT DOSE VIALS, 5mL Sterile 0.9% NaCl Solution for Inhalation USP. REF RHUD59U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V642000·2023-09-20

    2023 Chevrolet Tahoe and Related Models Suspension Bolt Recall

    General Motors is recalling certain 2023 Tahoe, Suburban, Escalade, Escalade ESV, Yukon, and Yukon XL vehicles due to improperly heat-treated rear suspension bolts that may break, risking wheel misalignment and crash.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE ESV, SUBURBAN, TAHOE, YUKON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2506-2023·2023-09-20

    Proclaim XR 7 Implantable Pulse Generators unable to exit MRI mode

    Abbott Medical is recalling Proclaim XR 7 Implantable Pulse Generators due to a malfunction that prevents patients from exiting MRI (Magnetic Resonance Imaging) mode, potentially disrupting normal device operation and therapy delivery.

    Product
    Proclaim" XR 7 Implantable Pulse Generator REF 3662 (previously known as Proclaim" 7 Elite IPG) Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2508-2023·2023-09-20

    Proclaim Plus 7 Implantable Pulse Generator Cannot Exit MRI Mode

    Abbott Medical recalled Proclaim Plus 7 Implantable Pulse Generators due to a defect preventing patients from exiting MRI mode. This operational failure could compromise device functionality during or after magnetic resonance imaging procedures.

    Product
    Proclaim Plus 7 Implantable Pulse Generator REF 3672 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It is powered by a hermetically sealed battery…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2511-2023·2023-09-20

    Infinity 7 Implantable Pulse Generator Recall Due to MRI Mode Exit Failure

    Abbott Medical recalls Infinity 7 Implantable Pulse Generators due to reports that patients cannot exit MRI mode. The FDA has classified this as a Class I recall affecting devices distributed worldwide.

    Product
    Infinity 7 Implantable Pulse Generator REF 6662 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It is powered by a hermetically sealed battery…
    Category
    Medical Device
    Distribution
    Distributed nationwide