The Recall Desk

State

Guam product recalls

73,388 recalls have nationwide distribution and so reach Guam. 386 additional recalls listed Guam specifically in their distribution scope.

What the numbers show

Total
386
Critical
14
Severe
54
Most recent
2026-09-23

Of the 386 recalls naming Guam we have scored against our rubric, 14 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 54 (14%) are Severe.

Which agencies issued them

These figures cover only the 386 recalls whose distribution notice names Guam specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18351–18375 of 73774

  • HighCPSC·23712·2022-12-01

    Polaris RZR Pro XP 4 Vehicles Recalled Due to Fire Hazard

    Polaris is recalling about 600 model year 2021-2022 RZR Pro XP 4 recreational off-road vehicles because a fuel leak at the fuel pump assembly joint can occur near a hot surface, creating a fire hazard. The company has received five reports of fuel leaks, including one report of fire, but no injuries have been reported.

    Product
    Model Years 2021-2022 RZR Pro XP 4 Recreational Off-Road Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23056·2022-12-01

    Cuisinart Compact Blender and Juice Extractor Combos Recalled for Laceration Hazard

    Conair is recalling about 66,000 Cuisinart Compact Blender & Juice Extractor Combos (Model CBJ-450) because the nut holding the blender blade assembly can loosen and detach during use, creating a laceration hazard.

    Product
    Cuisinart Compact Blender & Juice Extractor Combos Model CBJ-450
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23715·2022-12-01

    2022 Honda TRX90X ATVs Recalled Due to Stuck Throttle Cable

    American Honda is recalling about 2,900 2022 model year TRX90X ATVs because the throttle cable can get stuck, creating a crash and injury hazard. Consumers should stop using the vehicles and contact an authorized Honda Powersports dealer for a free inspection and repair.

    Product
    2022 model year Honda TRX90X ATVs
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23059·2022-12-01

    JBR Solutions Recalls Aduro Surge Protectors for Shock and Fire Hazards

    JBR Solutions is recalling about 51,750 Aduro surge protectors due to incorrect polarization and poorly soldered connections that pose shock and fire hazards. No injuries or fires have been reported.

    Product
    Aduro surge protectors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23058·2022-12-01

    The Laundress cleaning products recalled for bacterial contamination

    The Laundress is recalling approximately 8 million laundry and household cleaning products that may contain harmful bacteria including Burkholderia cepacia complex, Klebsiella aerogenes, and Pseudomonas species. People with weakened immune systems or underlying lung conditions face risk of serious infection.

    Product
    The Laundress laundry and household cleaning products
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23714·2022-12-01

    HABA USA Recalls Discovery Cubes Animal Hide and Seek Activity Toys

    HABA USA is recalling about 800 Discovery Cubes Animal Hide and Seek activity toys because the seam on the toy's house can open, allowing access to filling that poses choking and ingestion hazards for young children. No injuries have been reported.

    Product
    Discovery Cubes Animal Hide and Seek Activity Toy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23061·2022-12-01

    Summit Treestands Recalls Viper Level PRO SD Climbing Treestands for Fall Hazard

    Summit Treestands LLC is recalling about 2,555 Viper Level PRO SD climbing treestands because the tree cable can dislodge from the cable assembly, creating a fall hazard. No injuries have been reported.

    Product
    Viper Level PRO SD Treestands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23060·2022-12-01

    Target Recalls Cloud Island 4-Piece Plush Toy Sets for Choking Hazard

    Target is recalling Cloud Island 4-Piece Plush Toy Sets because the tires on the toy vehicles can detach, posing a choking hazard to children. The firm has received four reports of tires detaching but no injuries have been reported.

    Product
    Cloud Island 4-Piece Plush Toy Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0176-2023·2022-11-30

    Everything But The Sushi & Dumplings sauce recalled for undeclared soy

    Seed Ranch Flavor Co. is recalling Everything But The Sushi & Dumplings sauce due to undeclared soy allergen. Approximately 11,449 bottles were distributed nationwide and internationally.

    Product
    Everything But The Sushi & Dumplings, 5 fl. oz. (148 mL) glass bottle, UPC 8-60008-58851-7, Made for Seed Ranch Flavor Co., LLC Boulder, CO 80302. Ambient storage - minimum 35 degrees, maximum 85 degrees.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0174-2023·2022-11-30

    Umami Everyday Sauce recalled for undeclared soy allergen

    Umami Everyday Sauce is being recalled due to undeclared soy allergen. This poses a risk to consumers with soy allergies and sensitivities.

    Product
    Umami Everyday Sauce, 5 fl. oz. (148 mL) glass bottle, UPC 8-67732-00032-2, Made for Seed Ranch Flavor Co., LLC, Boulder, CO 80302 Ambient storage - minimum 35 degrees, maximum 85 degrees.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0238-2023·2022-11-30

    Mighty Bliss Electric Heating Pad recalled due to burn and shock hazard

    Whele LLC is recalling approximately 4,034 Mighty Bliss Electric Heating Pads due to burn and shock hazards. The firm received complaints of burns, mild electrical shocks, and skin irritation.

    Product
    Mighty Bliss Electric Heating Pad, Large (12 x 24 ) Grey Electric Heating Pad, PE-MtyBls-HeatPad-12x24-Gry-V2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0237-2023·2022-11-30

    Mighty Bliss Electric Heating Pad Recalled for Burn and Shock Risk

    Whele LLC is recalling the Mighty Bliss Electric Heating Pad due to burn and shock hazards. The company has received complaints of burns, electrical shocks, and skin irritation.

    Product
    Mighty Bliss Electric Heating Pad, Extra-Large (20 x 24 ) Blue Electric Heating Pad, MB-002
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0236-2023·2022-11-30

    Mighty Bliss Electric Heating Pad recalled for burn and shock hazards

    Whele LLC is recalling the Mighty Bliss Electric Heating Pad (model MB-001) due to burn and electrical shock hazards. The firm has received complaints of burns, shocks, and skin rashes from users.

    Product
    Mighty Bliss Electric Heating Pad, Large (12 x 24 ) Blue Electric Heating Pad, MB-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0175-2023·2022-11-30

    Umami Everyday Savory Spice Recalled for Undeclared Soy

    Umami Everyday Savory Spice is recalled nationwide due to undeclared soy. The product affects consumers with soy allergies and has been distributed in the US, Canada, UK, and France.

    Product
    Umami Everyday Savory Spice, 5 fl. oz. (148 mL) glass bottle, UPC 8-50000-72724-3, Co-Packed with Seed Ranch Flavor Co., Denver, CO 80216 Ambient storage - minimum 35 degrees, maximum 85 degrees.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0267-2023·2022-11-30

    Ventilator Screen Backlight Malfunction Causes Temporary Display Loss

    Hamilton-C6 ventilators are subject to a backlight malfunction causing the display screen to go black for 2-3 seconds. The FDA has classified this Class II recall as affecting 443 U.S. systems distributed nationwide.

    Product
    Hamilton-C6
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-11302022-01·2022-11-30

    USDA Issues Public Health Alert for Summer Sausage Due to Plastic Contamination

    USDA issued a public health alert for fully cooked summer sausage products from Paradise Locker Meats due to possible plastic contamination. No illnesses have been reported.

    Product
    Paradise Locker Meats — FSIS Issues Public Health Alert for Fully Cooked Summer Sausage Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0278-2023·2022-11-30

    PAJUNK Continuous Epidural Tray Recalled for Wrong Medication in Kit

    Pajunk Medical Systems is recalling PAJUNK Continuous Epidural Trays (Model TAL101, Lot 0001359) because some contain 0.75% Marcaine Spinal instead of the intended 0.9% Sodium Chloride. This medication substitution could lead to improper drug administration during epidural procedures.

    Product
    PAJUNK Continuous Epidural Tray, Tuohy Epidural Needle 17G x 4" with EpiLong Soft Catheter, Closed Tip, 19G, Model #TAL101, sterile, each tray contains 5ml Ampule 1% Lidocaine HCl, 10ml Ampule 0.9% Sodium Chloride, and 5ml Ampule 1.5% Lidocaine HCl with Epinephrine 1:200,000.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0282-2023·2022-11-30

    VS3 Iridium Visionsense Beam Combiner Optical Fiber Cable Damage Risk

    Visionsense VS3 Iridium beam combiners may develop damaged optical fiber cables through handling or bending, causing loss of functionality and potential cable heating or melting. Affected units were distributed nationwide in the US.

    Product
    VS3 Iridium Visionsense Infrared (IR) Fluorescence Light Integrator (Beam Combiner) Product Number: 161-0001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0166-2023·2022-11-30

    G FUEL Watermelon Limeade Energy Drink recalled for incorrect caffeine labeling

    G FUEL LLC is recalling 48,000 units of GFUEL brand Watermelon Limeade Energy Drink nationwide because the product label does not declare the correct amount of caffeine.

    Product
    GFUEL brand Watermelon Limeade Energy Drink; 16 fl. oz.; ready-to-drink energy beverage in a can
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0274-2023·2022-11-30

    Basin Set Medical Device Kit Contents Do Not Match Label

    American Contract Systems, Inc. is recalling a surgical basin set (MEBS42K) because the kit contents do not match the labeled contents. The mismatch could result in improper surgical preparation.

    Product
    BASIN SET, MEBS42K, general surgical kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0280-2023·2022-11-30

    Visionsense Infrared Microscope Recalled Due to Optical Fiber Cable Damage

    Visionsense is recalling 205 units of its VS3 Iridium microscope because optical fiber cables may become damaged during handling, causing loss of function and outer cable heating or melting.

    Product
    VS3 Iridium Visionsense Infrared (IR) Fluorescence Miniature Microscope (MMS-IR) Product Number: 174-0012
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0279-2023·2022-11-30

    Surgical Blade Safety Cartridges Recalled Due to Missing Sterilization

    Southmedic is recalling 450 units of sterile surgical blade cartridges (Lot W92761) because the product was not sterilized but was labeled and distributed as sterile. Non-sterile surgical blades could cause infection if used on patients.

    Product
    Southmedic SAFETY CARTRIDGE WITH SOUTHMEDIC PLUS SURGICAL BLADE, REF 73-8020, STERILE EO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0265-2023·2022-11-30

    B. Braun Central Venous Catheter Tray Recalled for Incorrect Expiration Date Label

    Medical Action Industries is recalling 240 cases of B. Braun CARESITE Port Access Kits (REF 375214) due to incorrect expiration date labeling. The kits show an expiration date of 02/21/2024 when the actual expiration is 02/10/2024.

    Product
    B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected 11/23/2022)
    Category
    Medical Device
    Distribution
    Distributed nationwide