The Recall Desk

State

Guam product recalls

72,940 recalls have nationwide distribution and so reach Guam. 385 additional recalls listed Guam specifically in their distribution scope.

What the numbers show

Total
385
Critical
14
Severe
37
Most recent
2026-01-28

Of the 385 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 37 (10%) are Severe.

These figures cover only the 385 recalls whose distribution notice names Guam specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4801–4825 of 73325

  • SevereCPSC·26023·2025-10-16

    Stone dining tables and desks recalled after one collapsed causing lacerations

    About 750 RH Byron travertine and marble tables and desks are being recalled because they can collapse; one dining table collapse has caused lacerations.

    Product
    Byron Emperador Tables and Byron Reeded Stone Tables and Desks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V706000·2025-10-16

    Alexis Fire Equipment Recalls Fire Trucks Due to Door Latch Defect

    Alexis Fire Equipment is recalling 22 fire trucks because a door latch defect may prevent the cab door from opening, potentially trapping occupants.

    Product
    ALEXIS FIRE EQUIPMENT — ALEXIS FIRE EQUIPMENT FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V704000·2025-10-16

    Chevrolet Equinox EV tires can lose tread partially or fully

    General Motors is recalling certain 2025-2026 Chevrolet Equinox EV and Cadillac Optic vehicles with 21-inch Continental all-season tires because one or more tires may lose part or all of their tread.

    Product
    CADILLAC — CADILLAC, CHEVROLET OPTIQ, EQUINOX EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26025·2025-10-16

    Rowing machines recalled after screen consoles caught fire or melted

    About 44,800 iFIT NordicTrack rowing machines are being recalled because the screen console can overheat and ignite; eight incidents include two fires and at least $6,000 in property damage.

    Product
    NordicTrack Model NTRW19147 Rowing Machine
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26026·2025-10-16

    Gas boilers recalled after cracked exhaust ducts leaked fumes indoors

    About 36,700 VST-brand residential gas boilers are being recalled after 33 reports of cracked exhaust ducts allowing exhaust fumes to leak, posing a carbon monoxide poisoning hazard.

    Product
    VST gas-fired tankless water heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26021·2025-10-16

    Personal transportation vehicles recalled over fuel leak at injector fitting

    About 90,800 E-Z-GO personal transportation vehicles are being recalled because fuel can leak at the quick-connect fitting between the fuel line and the fuel injector.

    Product
    E-Z-GO Personal Transportation Vehicles (PTVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26027·2025-10-16

    Yamaha golf cars recalled because the vehicles can fail to brake

    About 4,300 model year 2017-2024 Yamaha DR2A and DR2E personal transportation vehicles are being recalled because they can fail to brake. No incidents have been reported.

    Product
    Model Year 2017-2024 Yamaha Golf Car Vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26028·2025-10-16

    Yamaha golf cars recalled for lacking stop lights on the vehicle

    About 19,300 model year 2021-2025 Yamaha Drive 2 personal transportation vehicles are being recalled because they lack stop lights. No incidents have been reported.

    Product
    Model Year 2021-2025 Yamaha Golf Car Vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V705000·2025-10-16

    Land Rover and Jaguar Recall Vehicles for Gear Indicator Failure

    Jaguar Land Rover is recalling specific 2025-2026 models because moisture in the gear shift module may cause the gear position indicator light to fail, increasing crash risk.

    Product
    JAGUAR — JAGUAR, LAND ROVER F-PACE, RANGE ROVER EVOQUE, redundant RANGE ROVER, DISCOVERY SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0069-2026·2025-10-15

    Heart pump controllers recalled over potential operating system cybersecurity vulnerabilities

    Abiomed is recalling 10,153 Automated Impella Controllers over potential cybersecurity vulnerabilities related to the controller's operating system.

    Product
    Automated Impella Controller (AIC), used for left heart support blood pump, labeled as the following with corresponding Product Codes: 1. Impella Controller, Packaged, AU; Product Code: 0042-0000-AU. 2. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 3. Impella
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0035-2026·2025-10-15

    Infusion pump sets recalled over flow rate and occlusion alarm accuracy

    CareFusion is recalling BD Alaris Pump Infusion Sets because the pump module used with them may perform outside established ranges for flow rate, bolus accuracy and occlusion alarm timing.

    Product
    BD Alaris Pump Infusion Sets for the following reference numbers: C24101E, Amber Tubing, 15 Micron Filter, 0.2 Micron Filter, SmartSite Y-Site 10015414, 180 Micron Filter 2447-0007, Ball Valve SmartSite Port (Burette) 2 SmartSites Y-Sites 24201-0007, 2 SmartSite Y-sites
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0094-2026·2025-10-15

    NAD+ injection recalled after elevated endotoxin levels found in one lot

    GenoGenix is recalling NAD+ for Injection at 100 mg/mL and 200 mg/mL from one lot for microbial contamination of sterile products, with elevated endotoxin levels.

    Product
    NAD+ (Nicotinamide adenine dinucleotide) for Injection, a) 100 mg/mL b) 200 mg/mL, 10 mL multi-dose amber vials, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V700000·2025-10-15

    BMW Recalls 2018 328D Models Due to EGR Cooler Fire Risk

    BMW is recalling 2018 328D diesel vehicles because a leaking EGR cooler can cause smoldering particles and a melting intake manifold, increasing the risk of a fire.

    Product
    BMW — BMW 328D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0048-2026·2025-10-15

    Biotin for injection recalled across all lots over sterility assurance

    GenoGenix is recalling Biotin for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    Biotin for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0042-2026·2025-10-15

    Hydroxocobalamin B12 injection recalled across all lots for sterility assurance

    GenoGenix is recalling B12 Hydroxocobalamin for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    B12 Hydroxocobalamin for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0065-2026·2025-10-15

    NAD+ injection recalled across all lots for lack of sterility assurance

    GenoGenix is recalling NAD+ injection at 50 mg/mL and 100 mg/mL in 10 mL multi-dose vials, covering all lots within expiry, for lack of assurance of sterility.

    Product
    NAD+ (Nicotinamide adenine dinucleotide), a) 50 mg/mL, b) 100 mg/mL, 10 mL multi-dose vials, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for CELIA Health
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0058-2026·2025-10-15

    L-Glutamine for injection recalled across all lots over sterility assurance

    GenoGenix is recalling L-Glutamine for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    L-Glutamine for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0081-2026·2025-10-15

    Reconstitution XO solution recalled across all lots over sterility assurance

    GenoGenix is recalling Reconstitution XO Solution for Injection in all strengths and presentations, covering all lots within expiry, for lack of assurance of sterility.

    Product
    Reconstitution XO Solution for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for CELIA Health a) 5% Exosomes, 10 mL vial and b) 10% Exosomes, 5 mL vial, Extension Health a) 20% Exosomes,
    Category
    Drug
    Distribution
    Distributed nationwide