State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
RacerMate is recalling approximately 25,000 CompuTrainer Blue Flywheels because they can shatter during use, posing a risk of injury to riders and bystanders.
General Motors is recalling 2014-2016 Chevrolet Caprice Police Pursuit vehicles because corrosion may cause loss of electric power steering assist, increasing crash risk.
IKEA is recalling about 30,600 Gothem floor and table lamps because damaged cables can contact the metal body, posing a shock hazard. Consumers should stop using the lamps and return them for a full refund.
International Specialty Services is recalling Evercraft jack stands sold by NAPA Auto Parts because improper welds may cause the stands to collapse, posing an injury risk.
Rosenbauer is recalling 2012-2015 Commander vehicles because brake pedal pistons may corrode, making brakes difficult to activate or causing them to drag.
Battery-Biz is recalling Cyntur CTJSLI Lithium Ion Jumpstarters because a faulty cable design may cause overheating and fire. Owners should contact customer service for a free replacement cable.
Jayco is recalling 10 model year 2016 White Hawk travel trailers because they were built with axles rated for 3000 lbs instead of the required 3500 lbs, which may affect handling.
Winnebago is recalling 2016 Instinct trailers because an incorrect character may be stamped in the VIN. Dealers will replace the VIN plate at no cost.
Arrow International is recalling Percutaneous Insertion Trays because the sheath body may separate from the hub, creating a potential for bleeding.
Arrow International is recalling Ultra 8 IAB devices because the sheath body may separate from the hub, creating a potential for bleeding.
Arrow International is recalling UltraFlex IAB devices because the sheath body may separate from the hub, creating a potential for bleeding.
Arrow International is recalling RediGuard IAB devices because the sheath body may separate from the hub, creating a potential for bleeding.
Tf Supplements is recalling Rhino 7 3000 bottles because they contain undeclared desmethyl carbondenafil and dapoxetine and were marketed without an approved NDA or ANDA.
Tf Supplements is recalling Rhino 7 Platinum 3000 because it contains undeclared desmethyl carbondenafil and dapoxetine and was marketed without an approved NDA or ANDA.
Arrow International is recalling FiberOptix Ultra 8 IAB devices because the sheath body may separate from the hub, posing a risk of bleeding.
Hartley Medical Center Pharmacy is recalling specific hydromorphone and bupivacaine syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling specific hydromorphone and bupivacaine syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Sufentanil Cit 1000 mcg/ml/Baclofen 300 mcg/ml syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate and Bupivacaine syringes due to a lack of assurance of sterility.
Hartley Medical Center Pharmacy is recalling two syringes of Hydromorphone HCL 1 mg/ml because the agency could not ensure the product was sterile.
Hartley Medical Center Pharmacy is recalling specific hydromorphone and bupivacaine syringes due to a lack of assurance of sterility.
Stryker is recalling Position Pro Mattresses because the power cord may melt, posing risks of electric shock and fire.
Hartley Medical Center Pharmacy is recalling Morphine Sulfate and Baclofen syringes due to a lack of assurance of sterility. The affected products were distributed nationwide.
Arrow International is recalling Ultra 8 IAB devices because the sheath body may separate from the hub, creating a potential for bleeding.
Arrow International is recalling FiberOptix Ultra 8 IAB devices because the sheath body may separate from the hub, creating a risk of bleeding.