State
72,919 recalls have nationwide distribution and so reach Guam. 385 additional recalls listed Guam specifically in their distribution scope.
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.
Which agencies issued them
These figures cover only the 385 recalls whose distribution notice names Guam specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
ABC Bus is recalling specific Van Hool bus models because the front entrance door window may have incorrect glazing, which could reduce driver visibility and increase crash risk.
Petzl America is recalling Nomic and Ergonomic ice climbing axes because the shaft can break at the handle during use. Twenty-six shaft breakages have been reported, with no injuries.
Chrysler is recalling certain 2022–2026 Voyager and Pacifica vehicles because the right and left side curtain airbags may have insufficient pressure retention due to improperly sealed seams, increasing the risk of ejection and injury during a crash.
MPINOI adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and mattress, and the rails lack the required hazard warning labels.
DuraTrac is recalling stainless steel gas connectors sold between May and November 2025 because a manufacturing defect could cause a gas leak, posing a fire hazard.
Cardinal Health is recalling Webcol Alcohol Prep pads because of non-sterility, with microbial contamination identified as Paenibacillus phoenicis. The FDA has classified this recall as Class I.
Volvo Trucks is recalling certain 2025-2026 VNL (4) vehicles because the service brake may take longer than expected to release, creating a crash risk and violating Federal Motor Vehicle Safety Standard 121.
Nissan is recalling 2026 Leaf vehicles because internal damage in the high voltage battery may cause a short circuit, increasing the risk of a fire.
Strides Pharma is recalling two lots of Children's Ibuprofen Oral Suspension after complaints of a gel-like mass and black particles in the product.
Aston Martin is recalling certain 2025-2026 DBX and 2026 DBX S vehicles because the tire pressure monitoring system light may not illuminate to warn drivers of underinflated tires.
GE Medical Systems is recalling Centricity Universal Viewer software versions 5.0 SP6 through 5.0 SP7.1 because user login credentials may be exposed on the local client workstation.
ConvaTec is recalling one lot of the EsteemBody Drainable Pouch, REF 423653, because the drainable large pouch may leak due to a manufacturing issue.
ConvaTec is recalling two lots of the EsteemBody Drainable Pouch, REF 423643, because the drainable large pouch may leak due to a manufacturing issue.
GE Medical Systems is recalling Centricity Universal Viewer software versions 6.0 through 6.0 SP10.4.1 because user login credentials may be exposed on the local client workstation.
Somerset Therapeutics is recalling one lot of Dexamethasone Sodium Phosphate Injection after out-of-specification impurity results at product expiry during long term stability testing.
Volkswagen is recalling certain 2025 Jetta and Taos vehicles because the instrument panel may fail to display warning lights or gauges. This fails FMVSS 101.
Apotex is recalling two lots of Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution for lack of assurance of sterility.
ConvaTec is recalling one lot of the EsteemBody Drainable Pouch, REF 423657, because the drainable large pouch may leak due to a manufacturing issue.
Diagnostica Stago is recalling the STA Liatest D-Di kit after investigations confirmed a positive bias in D-dimer measurements throughout the entire analytical range.
Volvo Trucks is recalling certain 2025–2026 VNL (4) vehicles because the instrument panel may fail while driving, potentially hiding critical safety information like the speedometer and warning lights.
Baxter is recalling the Welch Allyn Spot Vision Screener VS100 on software version 3.2.0.1 because the display screen may unintentionally flicker, which may induce photosensitive seizure activity.
Abbott is recalling one lot of the ID NOW Influenza A & B 2 test after confirming the lot has a higher occurrence of invalid rates than stated in the Instructions for Use.
Elekta is recalling Leksell Gamma Knife radiosurgery systems, covering the Perfexion, Icon and Elekta Esprit models, due to an adapter not being properly aligned or locked in place.
GE Medical Systems is recalling Centricity Universal Viewer software versions 7.0 through 7.0 SP2.0.1 because user login credentials may be exposed on the local client workstation.
Hologic is recalling one master lot of the Aptima HPV Assay because the product exhibits potential to generate either invalid or false negative results.