State
72,797 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 72,797 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Kibbi is recalling 2026-2027 Renegade recreational vehicles because a rooftop fan component may overheat and cause a fire.
Loyoda adult portable bed rails are being recalled because they violate safety standards, posing risks of entrapment, asphyxiation, falls, and lacerations.
Daikin Comfort Technologies is recalling Amana Through-The-Wall air conditioners and heat pumps because a shorted component can cause fire and serious injury.
Audio Partnership is recalling Cambridge Audio Yoyo (M) Bluetooth speakers because their lithium-ion batteries can overheat and cause fires. No injuries have been reported.
Nanjing Wu Hai Smart Home Appliance Store is recalling Alanca 6-Drawer Dressers due to risks of serious injury or death from tip-over and entrapment.
Mondraker USA is recalling specific mountain bicycles equipped with ONOFF S9 Carbon MTB handlebars because they may crack or fracture, posing a risk of serious injury or death.
Gizoon Direct is recalling six-drawer double dressers due to tip-over and entrapment risks that can cause serious injury or death to children.
SHEIN is recalling about 963 Spiral Toys because they contain small balls that pose a choking hazard to children under three.
Skip Hop is recalling Baby Sesame Street Elmo Silicone Teethers because the black eyes can detach if frozen, posing a choking risk.
Clorox is recalling about 6.3 million bottles of scented Mistolin and Lestoil cleaners sold in Puerto Rico and the U.S. Virgin Islands due to potential bacterial contamination.
Truststone Group is recalling XO Poppy Power Trip Magnetic Wireless Power Banks because the lithium-ion batteries can overheat and ignite, posing fire and burn risks.
OKK Trading is recalling Rainbow Mystery Squishy Bun Toys because water beads inside can expand and cause choking or intestinal obstruction if swallowed.
Branch is recalling about 16,000 ergonomic chairs because the backrests can detach, posing a fall hazard. No injuries have been reported.
CPSC recalls GIHNJSI Squeezy Dumplings toys sold on Amazon due to water beads that pose serious ingestion, choking, and obstruction hazards.
Medline is recalling neonatal and infant heated wire breathing circuits due to a risk of sporadic failure and thermal damage at the humidifier connector.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 200 mcg tablets because they are subpotent. The recall covers distribution nationwide in the United States.
Fresenius Kabi is recalling Tyenne (tocilizumab-aazg) injection vials because an internal investigation found the presence of glass particles.
Accord Healthcare is voluntarily recalling Levothyroxine Sodium 300 mcg tablets because they may contain less active ingredient than labeled.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 50 mcg tablets nationwide because they may contain less than the labeled amount of active ingredient.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 100 mcg tablets because they may contain less active ingredient than labeled.
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium tablets because they may contain less active ingredient than labeled.
Medline is recalling 20 units of neonatal heated wire breathing circuits due to potential thermal damage that could cause airway obstruction or respiratory distress in infants.
Mallinckrodt is recalling ACTHAR Gel vials due to the presence of glass and stopper pieces. Patients should stop using the product and contact their healthcare provider.
B. Braun Medical Inc. is recalling 23,688 bags of Lactated Ringer's Injection USP due to the presence of particulate matter.
Church & Dwight is recalling Zicam Cold Remedy Nasal Swabs because FDA inspections found out-of-limit microbiological testing results at the contract manufacturer.