State
72,940 recalls have nationwide distribution and so reach Northern Mariana Islands. 22 additional recalls listed Northern Mariana Islands specifically in their distribution scope.
Of the 22 recalls naming Northern Mariana Islands we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 8 (36%) are Severe.
Which agencies issued them
These figures cover only the 22 recalls whose distribution notice names Northern Mariana Islands specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
About 22,600 IcyBreeze Buddy portable misting fans are recalled because the fan can overheat while charging and ignite. Seven overheating reports include two that resulted in fire; no injuries.
Ford is recalling 2023-2024 Transit vehicles previously repaired under recalls 24V226 and 24V591 due to potential installation of incorrect steering coupler covers and tires.
General Motors is recalling certain Cadillac Escalade, Chevrolet Tahoe and GMC Yukon diesel vehicles because the original fuel tank may have been replaced with an incorrect tank that can leak in a rollover.
Hyundai is recalling certain 2023-2025 Genesis GV60 electric vehicles because the stainless-steel molding at the top of the windshield assembly may detach.
About 21,690 Ambiano cotton candy makers, model 836098, are recalled because the heating element can ignite sugar if used without the sugar receptacle. Twelve sparking or fire reports; no injuries.
About 66,000 tabletop fire pits sold at Five Below are recalled because alcohol fuel can splash or leak during use or ignition, causing a flash fire. One report of flames escaping; no injuries.
About 5,460 Arizer Solo II portable vaporizers are recalled because the internal lithium-ion battery can overheat, produce smoke or eject material. Nine incidents have been reported; no injuries.
About 11,200 EnHomee Fabric 13-Drawer Dressers are recalled because they are unstable if not anchored to the wall and fail the mandatory STURDY Act standard. No incidents reported.
Volvo Trucks is recalling certain 2026 VNL trucks due to an incorrectly installed door latch cable that may prevent the interior door from opening, trapping occupants and increasing injury risk.
About 3,000 Youbeien crib mobiles are recalled because the button battery compartment in the remote can be opened without a common household tool, violating the mandatory toy standard.
Mack Trucks is recalling 2025-2026 Pioneer vehicles because trailer lights may fail to illuminate when towing, increasing crash risk.
About 1,780 YooxArmor multi-purpose kids' helmets in size small are recalled because they fail impact attenuation, positional stability, labeling and certification requirements. No incidents reported.
Volvo Trucks is recalling certain 2025–2026 VNL and 2025 VNR trucks because the trailer body control module may be improperly manufactured, causing trailer lights to fail to illuminate and reducing visibility.
About 360 LXDHSTRA baby loungers are recalled because they violate the mandatory Infant Sleep Products standard and are supplied with padded crib bumpers banned by the Safe Sleep for Babies Act.
ViziShot 2 FLEX single use aspiration needles, model NA-U403SX-4019, are recalled because of the potential for undetected, deformed atraumatic tips. The FDA classified the action as Class I. 104,508 units are affected.
LinkSymphoKnee modular TiNbN tibial components, size 5, REF 880-100/50, are recalled because some were manufactured with two uncoated security screws. 8 units are affected.
Halyard CPT Basic IR Packs, model 1646381, are recalled because of the potential for open header bag seals, compromising sterility. 228 units are affected.
DJO Surgical FA S Altivate Reverse Glenoid Tray kits are recalled across all lots because the reamer may kick or bind up during or immediately prior to use. 439 kits are affected.
TiBrid SA Angled Punch Awls in 30, 45 and 60 degree sizes are recalled following failure of fusion system instruments in the field. 15 units are affected.
Atellica CH Urinary/Cerebrospinal Fluid Protein assay is recalled because of the potential for falsely depressed patient, quality control and calibration results, or delayed results. 11,811 units are affected.
Zydus Chlorpromazine Hydrochloride Tablets, USP, 10 mg, are recalled nationwide because N-Nitroso Desmethyl Chlorpromazine was found above the recommended acceptable intake limit.
10Fore Hemostasis Valves are recalled because of a manufacturing issue where the silicone quad ring is deformed or damaged and may cause a foreign body in the fluid pathway. 447 units are affected.
Halyard ENT Packs, model JACK421-04, lot 1647218, are recalled because of the potential for open header bag seals, compromising sterility. 57 units are affected.
DJO Surgical Altivate Reverse Wedge Glenoid Reamer Sleeves are recalled across all lots because the reamer may kick or bind up during or immediately prior to use. 447 units are affected.
TiBrid SA Angled Screwdrivers in 30, 45 and 60 degree sizes are recalled following failure of fusion system instruments in the field. 15 units are affected.