State
72,969 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 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Séfralls Hair Generation Serum is being recalled because it contains minoxidil, which must be in child-resistant packaging under the Poison Prevention Packaging Act. About 21,300 units affected.
Suzuki is recalling 2020-2025 DL1050 and 2020/2024 GSX-S1000S motorcycles because the upper headlight beam may be too bright, potentially blinding oncoming drivers.
Mitsubishi is recalling certain 2018–2022 Outlander PHEV and 2014–2020 Outlander vehicles because liftgate gas spring cylinders may corrode, lose pressure, rupture, or cause the liftgate to fall unexpectedly, creating injury risk.
Pet Zone Laser Pointer & LED Ball pet toys are being recalled because the LED sphere can break on impact, making the button cell batteries easily accessible to children. About 15,400 units affected.
Nissan is recalling certain 2025 Nissan Frontier vehicles due to a software logic error that may cause daytime running lights to dim unexpectedly when the idle start-stop feature cycles the engine, posing a crash risk.
Fontaine Modification is recalling 2022–2024 Freightliner Business Class M2 vehicles because welds on the intermediate steering shaft may crack and fail, causing loss of steering control and crash risk.
International Motors is recalling certain 2016–2024 IC Bus CESB school buses because the brake pressure switch assembly may leak brake fluid into electrical components, causing a short circuit and fire risk while driving or parked.
SafeStar 55 Plus bidirectional breathing system filters are being recalled following reports of a slow increase of the CO2 curve when the gas sample is taken from the filter's port. 9,885,139 units affected.
SafeStar 90 Plus bidirectional breathing system filters are being recalled following reports of a slow increase of the CO2 curve when the gas sample is taken from the filter's gas sampling port. 669,838 units affected.
HME TwinStar HEPA Plus bidirectional breathing system filters are being recalled following reports of a slow increase of the CO2 curve when the gas sample is taken from the filter's port. 1,019,782 units affected.
Coaxial breathing circuit sets for HAMILTON-C1, T1 and MR1 ventilators are being recalled because the blue tubing that delivers fresh gas may be cracked, which can cause rebreathing of exhaled gases. 2,560 units affected.
SafeStar 60A Plus bidirectional breathing system filters are being recalled following reports of a slow increase of the CO2 curve when the gas sample is taken from the filter's port. 374,700 units affected.
International Motors is recalling certain 2018–2025 International 4000 Series, MV, 1300 FBC, and IC Bus TC and CECB vehicles. A leaking brake pressure switch assembly may cause an electrical short circuit that increases fire risk while driving or parked.
The Automated Impella Controller, used with left heart support blood pumps, is being recalled because of a potential issue with the controller not detecting an Impella pump when it is connected. 11,031 units affected.
MR 5300 systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 551 units are affected.
Ingenia 1.5T S MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 136 units are affected.
SmartPath to dStream for 3.0T systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 15 units affected.
Evolution Upgrade 1.5T MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 93 units are affected.
Ingenia Elition X MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 632 units are affected.
Dual Flat Panel Monitor accessories for HarmonyAIR A-Series Surgical Lighting Systems are being recalled because the yoke assembly may detach from the spring arm. 167 units are affected.
Osteotec Silicone Finger Implants in sizes 3, 4 and 5 are being recalled because there is the potential that the silicone implant may contain foreign material. 15,573 units are affected.
Volcano Visions Digital IVUS Catheters are being recalled following reports of catheter and guide wire entanglement during radial-to-peripheral procedures, which may require surgical removal. 233,817 units affected.
HeartSine SAM 350P, 360P and 450P public access defibrillators are being recalled because a component manufacturing issue means the device may not function properly to deliver shocks. 190,516 units affected.
SmartPath to Ingenia Elition X systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 33 units affected.
Blood/EMB Levine plates, product number R02041, are being recalled because the products may contain surface and subsurface contamination of Listeria monocytogenes. 750 units are affected.