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.
Sun Pharmaceutical Industries is recalling 393 vials of Doxorubicin Hydrochloride Liposome Injection due to a lack of assurance of sterility.
Toyota is recalling 48,672 vehicles because air bag sensors may fail, preventing deployment in a crash and increasing injury risk.
International Laboratories, Inc. is recalling Pravastatin Sodium Tablets, 20 mg, because bottles may contain 10 mg tablets. Patients should contact their healthcare provider.
Nissan is recalling 2015-2017 Juke Nismo RS vehicles because brake fluid may leak into the brake booster, reducing brake performance and increasing crash risk.
Vyaire Medical is recalling 16,670 AirLife Humidification Chambers and circuits because a manufacturing error may cause water to back up into patient airways.
Philips is recalling Brilliance iCT CT systems due to software issues affecting scan functions and safety features.
John Deere is recalling about 600 model 2025R compact utility tractors because the brakes can fail, posing crash and injury hazards.
Siemens is recalling 36 units of Syngo Imaging version V31 software due to a potential risk of data loss relevant to diagnosis.
DLC Laboratories is recalling Earth's Care Eczema Lotion due to microbial contamination. The product was distributed nationwide.
LEDVANCE is recalling SYLVANIA recessed canister light kits because they can short circuit, posing a shock and electrocution hazard.
Triumph is recalling 2016-2018 Thruxton motorcycles because the engine may stall during rapid throttle changes, increasing crash risk.
Philips Medical Systems is recalling 559 Brilliance iCT CT systems due to software issues affecting scan functions and safety features.
Marksans Pharma Inc. is recalling 4,127,500 ibuprofen tablets due to odor complaints and CGMP deficiencies. The product was distributed nationwide to repackaging firms.
Odan Laboratories is recalling 179 kits of Dry to Normal Skin Starter Kit because the product failed stability specifications at 12 months.
Marksans Pharma Inc. is recalling 21,584,100 Ibuprofen Tablets, USP 400 mg, due to odor complaints linked to CGMP deficiencies.
Marksans Pharma Inc. is recalling 52,549,000 ibuprofen tablets due to odor complaints and CGMP deficiencies. The product was distributed nationwide.
Marksans Pharma Inc. is recalling specific lots of 600 mg ibuprofen tablets due to odor complaints linked to CGMP deficiencies.
Marksans Pharma Inc. is recalling 205,088,000 ibuprofen tablets due to odor complaints linked to CGMP deficiencies. The product was distributed nationwide in the USA.
Intuitive Surgical is recalling 60 da Vinci Xi EndoWrist Stapler 45 instruments due to a manufacturing variation that may prevent the release wrench from unclamping the device.
Odan Laboratories is recalling 21 jars of Day Cream SPF15 because the product failed stability specifications at 12 months.
Marksans Pharma Inc. is recalling ibuprofen tablets due to odor complaints linked to Current Good Manufacturing Practice (CGMP) deficiencies.
Measurement Specialties Inc. is recalling 6,076 reusable temperature probes because their sterilization instructions have not been proven through a validation study.
Mylan Pharmaceuticals is voluntarily recalling specific bottles of bupropion HCL extended-release tablets due to out-of-specification impurities found during routine stability testing.
Forest River is recalling 2018 Georgetown recreational vehicles because undersized wiring may melt and cause a fire. Dealers will install an additional circuit breaker free of charge.
Volkswagen Group of America is recalling specific Audi models because the driver's air bag inflator may explode during deployment, potentially causing serious injury or death.