The Recall Desk

State

Puerto Rico product recalls

72,811 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 72,811 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26–50 of 75901

  • SevereFDA (Food)·H-1269-2026·2026-09-02

    Outshine Fruit Bars Recalled for Potential Glass Contamination

    Dreyer's Grand Ice Cream Inc. is recalling Outshine Fruit Bars because they may contain glass pieces. Consumers should check for specific batch codes.

    Product
    Outshine Fruit Bars Strawberry, Pineapple, Grape, Tangerine. 24-Count 2.5 ounce, UPC 041548816678, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Food)·H-1264-2026·2026-09-02

    Outshine Strawberry Fruit Bars Recalled for Potential Glass Contamination

    Dreyer's Grand Ice Cream Inc. is recalling Outshine Strawberry Fruit Bars because they may contain glass pieces.

    Product
    Outshine Fruit Bars Strawberry, 6-Count 2.5 ounce, with UPC 041548610047, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Drugs)·D-0779-2026·2026-09-02

    Accord Healthcare Recalls Subpotent Levothyroxine Sodium Tablets Nationwide

    Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 100 mcg tablets because they may contain less active ingredient than labeled.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0790-2026·2026-09-02

    Zicam Cold Remedy Nasal Swabs Recalled for Microbiological Testing Failures

    Church & Dwight is recalling Zicam Cold Remedy Nasal Swabs because FDA inspections found out-of-limit microbiological testing results at the contract manufacturer.

    Product
    Zicam, Cold Remedy, Medicated Nasal Swabs, With Cooling Menthol & Eucalyptus, 20 Single-Use Swabs per carton, Zinc-Free Homeopathic, Distributed by Church & Dwight Co. Inc., Ewing, NJ 08628, UPC 732216301205.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0778-2026·2026-09-02

    Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide

    Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium tablets because they may contain less active ingredient than labeled.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2991-2026·2026-09-02

    Medline Neonatal Heated Wire Breathing Circuits Recalled for Thermal Failure

    Medline is recalling 20 units of neonatal heated wire breathing circuits due to potential thermal damage that could cause airway obstruction or respiratory distress in infants.

    Product
    Medline Hudson RCI, DBD-CIRCUIT,VENT,INSPIRATORY,HEATED,NEO, Medline Product Number/SKU HUD78019 (Teleflex Product Number/SKU 780-19); breathing circuit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0827-2026·2026-09-02

    Fresenius Kabi Recalls Tyenne Injection Due to Glass Particles

    Fresenius Kabi is recalling Tyenne (tocilizumab-aazg) injection vials because an internal investigation found the presence of glass particles.

    Product
    TYENNE — TYENNE (TOCILIZUMAB-AAZG)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0803-2026·2026-09-02

    ACTHAR Gel Recalled for Presence of Glass and Stopper Particulate Matter

    Mallinckrodt is recalling ACTHAR Gel vials due to the presence of glass and stopper pieces. Patients should stop using the product and contact their healthcare provider.

    Product
    ACTHAR — ACTHAR (REPOSITORY CORTICOTROPIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0786-2026·2026-09-02

    Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide

    Accord Healthcare is voluntarily recalling Levothyroxine Sodium 300 mcg tablets because they may contain less active ingredient than labeled.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1266-2026·2026-09-02

    Outshine Fruit Bars Grape Recalled for Potential Glass Contamination

    Dreyer's Grand Ice Cream Inc. is recalling Outshine Fruit Bars Grape due to the potential presence of glass pieces.

    Product
    Outshine Fruit Bars Grape, 6-Count 2.5 ounce, with UPC 041548244044, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Drugs)·D-0832-2026·2026-09-02

    B. Braun Recalls Lactated Ringer's Injection Due to Particulate Matter

    B. Braun Medical Inc. is recalling 23,688 bags of Lactated Ringer's Injection USP due to the presence of particulate matter.

    Product
    LACTATED RINGERS — LACTATED RINGERS (SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1265-2026·2026-09-02

    Outshine Watermelon Fruit Bars Recalled for Potential Glass Contamination

    Dreyer's Grand Ice Cream Inc. is recalling Outshine Watermelon Fruit Bars because they may contain glass pieces.

    Product
    Outshine Fruit Bar Watermelon, 6-Count 2.5 ounce with UPC 041548413624, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Drugs)·D-0776-2026·2026-09-02

    Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide

    Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 50 mcg tablets nationwide because they may contain less than the labeled amount of active ingredient.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0785-2026·2026-09-02

    Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide

    Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 200 mcg tablets because they are subpotent. The recall covers distribution nationwide in the United States.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1267-2026·2026-09-02

    Outshine Tangerine Fruit Bars Recalled for Potential Glass Contamination

    Dreyer's Grand Ice Cream Inc. is recalling Outshine Tangerine Fruit Bars because they may contain glass pieces.

    Product
    Outshine Fruit Bars Tangerine, 6-Count 2.5 ounce, with UPC 041548612041, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Food)·H-1268-2026·2026-09-02

    Outshine Black Cherry Fruit Bars Recalled for Potential Glass Contamination

    Dreyer's Grand Ice Cream Inc. is recalling Outshine Black Cherry Fruit Bars because they may contain glass pieces. Consumers should stop eating the product.

    Product
    Outshine Fruit Bars Black Cherry, 6 Bars, 2.5 ounce, with UPC 041548000121, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2993-2026·2026-09-02

    Medline Neonatal Heated Wire Breathing Circuits Recalled for Thermal Damage Risk

    Medline is recalling neonatal and infant heated wire breathing circuits due to a risk of sporadic failure and thermal damage at the humidifier connector.

    Product
    Medline breathing circuits labeled as: 1) MEDLINE HUDSON RCI, CIRCUIT, NEO, SING LIMB, HTD,COLUMN, Medline Product Number/SKU HUD78001KIT (Teleflex Product Number/SKU 780-01KIT); 2) MEDLINE HUDSON RCI, CIRCUIT, NEO, DUAL LIMB HTD, COLUMN, Medline Product Number/SKU HUD78007K
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3023-2026·2026-09-02

    Medline Convenience Kits Recalled for Potentially Contaminated Component

    Medline Industries is recalling 15 convenience kits (SKU CDS980375M) due to a potentially contaminated component. The kits were distributed in 18 US states.

    Product
    Medline convenience kits labeled as: LTP CDS-LF, Medline kit SKU CDS980375M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-1277-2026·2026-09-02

    Byron White Herbal Supplement Recalled for Undeclared Walnut Allergen

    Byron White Formulas is recalling its A-P Herbal Supplement because the label fails to declare walnuts in English, posing a risk to individuals with nut allergies.

    Product
    Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404
    Category
    Food
    Distribution
    50 states
  • HighFDA (Food)·H-1276-2026·2026-09-02

    Byron White A-L Complex Herbal Supplement Recalled for Undeclared Walnut

    Byron White Formulas is recalling A-L Complex Herbal Supplement because the label does not declare walnuts in English, posing a risk to individuals with nut allergies.

    Product
    Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404
    Category
    Food
    Distribution
    50 states
  • HighFDA (Devices)·Z-2996-2026·2026-09-02

    Medline Neurosponge Kits Recalled for Endotoxin Levels

    Medline is recalling 3,468 neurosurgical convenience kits containing Pilling Wecksorb Neurosponges due to potential out-of-specification endotoxin levels.

    Product
    Medline medical convenience kits, labeled as: 1) NEURO CDS, Medline Kit SKU CDS985246J; 2) NEURO PACK, Medline Kit SKU DYNJ32770V; 3) NEURO BUNDLE-LF, Medline Kit SKU DYNJ40095D; 4) NEURO PACK-LF, Medline Kit SKU DYNJ42844D; 5) NEURO PACK, Medline Kit SKU DYNJ45121I;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3031-2026·2026-09-02

    Healthmark ProChek-II Medical Tests Recalled for Expired Ingredient

    Healthmark Industries is recalling ProChek-II tests because they were manufactured with an expired ingredient, which may cause false negative or positive results.

    Product
    healthmark ProChek-II, Model Number PT-313, PT-201-12
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2988-2026·2026-09-02

    Philips Incisive CT Recalled for Potential Failure to Trigger Clinical Scan

    Philips is recalling Incisive CT scanners with specific software versions due to a potential failure to trigger clinical scans during bolus tracking.

    Product
    Philips Incisive CT with software V4.5&V5.0, Product Code 728143 and Product Code 728144.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3004-2026·2026-09-02

    Merge Healthcare Recalls PACS Workstations Due to Inaccurate Measurements

    Merge Healthcare is recalling 20 Merge PACS and Merge OrthoPACS workstations because a software issue may cause measurements to be displayed inaccurately.

    Product
    Merge PACS and Merge OrthoPACS, medical imaging diagnostic workstation
    Category
    Medical Device
    Distribution
    Distributed nationwide