State
73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Hale Products Inc. is recalling SmartFoam 6.5-12 foam pump systems with 12-volt power supplies because they can overheat and fail, rendering fire-fighting foam unavailable.
Southwire is recalling about 3,000 Garvin Pop-Up Electrical Outlet Floor Box Kits because the receptacles can overheat, posing a fire hazard. No injuries have been reported.
Crate and Barrel is recalling about 1,500 Activity Push Walkers because they can expose sharp points and small parts, posing choking and laceration hazards to small children.
Newmar is recalling 2018-2020 King Aire, Mountain Aire, and Essex motorhomes because the bedroom fascia header may fall onto the bed, increasing injury risk.
Club Car is recalling approximately 1,300 gas utility and transport vehicles because a fuel vent may leak fuel, posing a fire hazard. No injuries have been reported.
Manac is recalling 2011-2020 Flatbed trailers because twistlocks may rotate to unlock, risking container detachment and crashes.
Halcore Group is recalling 2018-2020 Horton Type I and III emergency vehicles because air bag cushions may detach and fail to inflate during a crash.
Club Car is recalling about 9,000 gas-powered golf and transport vehicles because a fuel line may leak, posing fire and burn hazards.
PACCAR is recalling 2020 Kenworth T270 and T370 trucks because loose fittings may cause the brake air hose to separate, reducing braking ability.
Forest River is recalling 2019 Rockport box vans and service bodies because improperly welded bulk storage beams may fail when loaded, posing an injury risk.
Mercedes-Benz is recalling 2019 CLS 450 vehicles because an electrical line may chafe, causing engine stalls or electrical system failures that increase crash risk.
Tyson Foods is recalling approximately 39,078 pounds of Weaver brand frozen chicken patties due to possible foreign matter contamination. Consumers should not consume these products.
Capco USA is recalling CTR Outer Tie Rods because the taper on the ball studs may affect durability. This defect could impact vehicle control and increase crash risk.
Altec is recalling 2012-2019 aerial devices because a winch valve defect may allow lifting beyond rated capacity, increasing injury risk.
Jaguar Land Rover is recalling 2018 Range Rover and Range Rover Sport vehicles because the backup camera may fail to display the rearview image, increasing crash risk.
SSR Motorsports is recalling 2019 off-road competition motorcycles because the front fork assembly can fail, causing a crash and injury hazard.
RXQ Compounding LLC is recalling Ondansetron 2 mg/mL Injection Solution because the product lacks assurance of sterility.
RXQ Compounding LLC is recalling Inositol/Choline B12:B6 injection solution because there is a lack of assurance of sterility.
St Jude Medical is recalling 21 Ellipse DR implantable cardioverter defibrillators due to damaged aluminum wires that may prevent the delivery of high-voltage therapy.
RXQ Compounding LLC is recalling Hydroxocobalamin 1000 mcg/mL injections because the product lacks assurance of sterility. The recall covers all lots within expiry distributed nationwide.
RXQ Compounding LLC is recalling Sodium Bicarbonate 8.4% Injection due to a lack of assurance of sterility. The product is distributed nationwide.
RXQ Compounding LLC is recalling MIC (Methionine/Inositol/Choline Chloride) 25/50/50 mg/mL Injection due to a lack of assurance of sterility.
RXQ Compounding LLC is recalling Buffered Lidocaine 1%+Epi 1:100,000 Injection Solution because the product lacks assurance of sterility.
St Jude Medical is recalling 15 Ellipse DR cardioverter defibrillators due to damaged aluminum wires that may prevent high-voltage therapy delivery.
RXQ Compounding LLC is recalling magnesium, calcium, and zinc vials due to a lack of assurance of sterility. The products were distributed nationwide.