The Recall Desk

State

Puerto Rico product recalls

72,940 recalls have nationwide distribution and so reach Puerto Rico. 3,090 additional recalls listed Puerto Rico specifically in their distribution scope.

What the numbers show

Total
3,090
Critical
366
Severe
625
Most recent
2026-09-02

Of the 3,090 recalls naming Puerto Rico we have scored against our rubric, 366 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 625 (20%) are Severe.

These figures cover only the 3,090 recalls whose distribution notice names Puerto Rico specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4726–4750 of 76030

  • SevereCPSC·26046·2025-10-23

    Curling irons recalled after 258 reports of the barrel detaching

    About 357,000 Bio Ionic one-inch long barrel curling irons are being recalled after 258 reports of the barrel snapping and detaching, including six minor burn injuries.

    Product
    Bio Ionic One-Inch-Long Barrel Curling Iron
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V721000·2025-10-23

    Ford Bronco front seat pivot bolts may be loose or dislodged

    Ford is recalling certain 2021-2023 Bronco vehicles because the front seats may have a loose or dislodged seat frame height-adjust pivot bolt, so the seat may not restrain an occupant in a crash.

    Product
    FORD — FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V724000·2025-10-23

    Wartech SpecialContainer Trailers Recalled for Brake Fitting Leak Risk

    Wartech is recalling 2022-2025 SpecialContainer trailers because an incorrect piping fitting may leak air, reducing brake pressure and increasing crash risk.

    Product
    WARTECH — WARTECH SPECIALCONTAINER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V720000·2025-10-23

    Ram ProMaster radiator fan electrical circuit can overheat

    Chrysler is recalling certain 2018-2026 Ram ProMaster vehicles because the electrical circuit for the radiator fan may overheat, increasing the risk of a fire.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26037·2025-10-23

    Adult portable bed rails recalled over entrapment and asphyxiation risk

    LEACHOI Bed Rails are being recalled because users can become entrapped within the rail or between the rail and the mattress, and the rails lack required hazard warning labels.

    Product
    LEACHOI Bed Rail
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V722000·2025-10-23

    Maserati headlights may be missing their adjustment prevention caps

    Maserati is recalling certain 2023-2025 Grecale, Granturismo and Grancabrio vehicles because the headlights may be missing adjustment prevention caps, allowing them to be improperly adjusted.

    Product
    MASERATI — MASERATI GRECALE, GRANTURISMO, GRANCABRIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26047·2025-10-23

    Gas and oil fuel containers recalled over flash fire and poisoning risks

    About 840 Scepter B62 gas and oil combination fuel containers are being recalled because they lack flame mitigation devices and the spout is not child-resistant.

    Product
    Scepter Gas and Oil Combination Fuel Containers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26049·2025-10-23

    Five drawer dressers recalled over tip over and entrapment hazards

    About 410 Bealife 5-drawer dressers sold on Amazon are being recalled because they are unstable when not anchored to a wall and violate the STURDY Act standard.

    Product
    Bealife 5-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0051-2026·2025-10-22

    BF-1TQ180 bronchovideoscopes recalled for updated therapy equipment use instructions

    Olympus is recalling EVIS EXERA II Bronchovideoscope BF Type 1TQ180 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.

    Product
    EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE 1TQ180
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0061-2026·2025-10-22

    BF-Q180 bronchovideoscopes recalled for updated laser and coagulation instructions

    Olympus is recalling EVIS EXERA II Bronchovideoscope BF Type Q180 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.

    Product
    EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0015-2026·2025-10-22

    Compounded oxytocin bags recalled after testing found no oxytocin present

    IntegraDose Compounding Services is recalling 853 bags of Oxytocin 30 Units/500 mL in 0.9% sodium chloride after testing revealed there was no oxytocin in the IV bag.

    Product
    Oxytocin 30 Units/500 mL in 0.9% Sodium Chloride for intravenous use, Rx only, IntegraDose Compounding Services LLC, 719 Kasota Ave Se, Minneapolis, MN 55414-2842 NDC 71139-0012-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0058-2026·2025-10-22

    BF-P60 bronchofiberscopes recalled for updated instructions on laser and coagulation use

    Olympus is recalling OES Bronchofiberscope BF Type P60 units for additional instructions-for-use updates clarifying safe use with laser, argon plasma coagulation and high-frequency therapy equipment.

    Product
    OES BRONCHOFIBERSCOPE OLYMPUS BF TYPE P60
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0056-2026·2025-10-22

    BF-P180 bronchovideoscopes recalled for updated therapy equipment use instructions

    Olympus is recalling EVIS EXERA II Bronchovideoscope BF Type P180 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.

    Product
    EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE P180
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0062-2026·2025-10-22

    BF-Q180-AC bronchovideoscopes recalled for updated laser and coagulation use instructions

    Olympus is recalling EVIS EXERA II Bronchovideoscope BF Type Q180-AC units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.

    Product
    EVIS EXERA II BRONCHOVIDEOSCOPE OLYMPUS BF TYPE Q180-AC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0050-2026·2025-10-22

    BF-1TQ170 bronchovideoscopes recalled for updated instructions on laser use

    Olympus is recalling Bronchovideoscope BF-1TQ170 units for instructions-for-use updates on safe use with laser, argon plasma coagulation and high-frequency therapy equipment.

    Product
    BRONCHOVIDEOSCOPE OLYMPUS BF-1TQ170
    Category
    Medical Device
    Distribution
    Distributed nationwide