State
73,741 recalls have nationwide distribution and so reach Northern Mariana Islands. 23 additional recalls listed Northern Mariana Islands specifically in their distribution scope.
Of the 23 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 18 (78%) are Severe.
Which agencies issued them
These figures cover only the 23 recalls whose distribution notice names Northern Mariana Islands specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Libbey Glass is recalling approximately 229,000 Bourbon Taster Glasses because they can break during normal use, posing a laceration hazard.
Medline Industries is recalling 1,428 plastic transfer belts because the locking mechanism may fail, allowing the strap to slip through the buckle.
Zimmer Biomet is recalling 29 ROSA Surgical Devices due to a software issue affecting cooperative endoscopy mode.
Leading Pharma, LLC is recalling Lorazepam tablets labeled as 0.5 mg but containing 1 mg. The recall addresses a labeling error affecting 2,952 bottles nationwide.
West-Ward Pharmaceuticals is recalling specific lots of Dexamethasone Sodium Phosphate Injection because of high out-of-specification results for a related compound.
West-Ward Pharmaceuticals is recalling Dexamethasone Sodium Phosphate Injection due to high levels of a related compound impurity.
Zero Motorcycles is recalling 36 units of 2018 motorcycles because the Vehicle Emission Control Information label may display the wrong model year.
Daimler Trucks North America is recalling 2008-2018 Freightliner and Western Star trucks because the brake light switch may fail to activate lights after hard braking, increasing crash risk.
Gulf Stream Coach is recalling 2018 Geo and Breeze trailers because the Federal label incorrectly lists two axles instead of one, failing certification requirements.
doTERRA is voluntarily recalling Slim & Sassy TrimShake mixes because they contain an undeclared milk allergen.
doTERRA is voluntarily recalling Slim & Sassy TrimShake chocolate and vanilla mixes because they contain an undeclared milk allergen.
DRV Suites is recalling specific recreational vehicles equipped with certain Kidde fire extinguishers that may clog, require excessive force to activate, or have nozzles that detach.
WalkMed, LLC is recalling 25,920 infusion pump reservoir bags due to reported fluid leaks at the luer connection.
Aurora Products is recalling Dark Chocolate Cherries in 8.5 oz cups and 11 oz tubs due to undeclared milk.
Bison Coach is recalling 2010 Stratus, Aluma Sport, Trail Express, and Trail Hand trailers because their fire extinguishers may clog or detach, posing injury risks.
Zimmer Biomet is recalling 21 ROSA Surgical Devices due to a possible break in the Force Sensor connector. The devices were distributed to facilities in Ohio, Michigan, and Texas.
Zimmer Biomet is recalling 53 ROSA Surgical Devices because of observed instability. The devices are computer-controlled arms used in neurosurgery.
Entegra is recalling 2010-2011 Aspire, Anthem, and Cornerstone RVs because the installed fire extinguishers may clog, require excessive force to activate, or have nozzles that detach.
Goal Zero is recalling Street Charge solar powered charging stations because a weld failure could cause the top post to fall, posing an impact hazard.
Prevost is recalling specific aftermarket commercial bus driver seats because the seat belt buckle may be stuck in the locked position, preventing the seat belt from latching.
Aurora Products is recalling Dark Chocolate Almonds nationwide and in Bermuda because the product contains undeclared milk.
KME is recalling 74 fire trucks because corroding rings may cause pressure relief valves to open, reducing water pressure for firefighting.
Aurora Products is recalling Dark Chocolate Turbinado Almonds with Sea Salt because the product contains undeclared milk. The recall affects 1,128 units distributed nationwide and in Bermuda.
ICU Medical is recalling 21,461 Plum 360 Infusion Systems because a software defect can prevent users from stopping the pump or restarting delivery under specific conditions.
Aurora Products is recalling Dark Chocolate Cranberries because the product contains undeclared milk, a major food allergen.