State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Robert Rothschild Farm LLC is recalling Gift Sets with Chocolate Pretzel Dippers because the product is not labeled with an ingredient statement, failing to declare the allergens soy and wheat.
Siemens is recalling IMMULITE 2000 Progesterone kits because DHEA-S causes falsely elevated results, potentially affecting diagnosis.
Nu Skin Enterprises is voluntarily recalling Pharmanex Cholestin softgels because the product contains undeclared soy, a common allergen.
VanLeigh is recalling 2016-2017 Vilano fifth-wheel trailers because incorrect Federal Placard information may lead to vehicle overloading.
Villa Sistemi Medicali is recalling 65 Juno DRF x-ray systems because the footrest can detach from the table, causing patients to fall.
Advanced Sports International is recalling about 650 2017 Fuji bicycles because the rear wheel freehub can slip while pedaling, posing a fall hazard.
Nu Skin Enterprises is voluntarily recalling Pharmanex BioGinkgo tablets because they contain undeclared wheat, a major food allergen.
Mako Surgical Corporation is recalling 777 MAKO RIO THA Application User Guides because five AFMEA Risk Control Measures are missing from the documents.
Remel Inc is recalling Haemophilus Test Medium agar plates because poor organism growth may result in incorrect susceptibility test results.
Actavis Inc is recalling specific lots of Levofloxacin Ophthalmic Solution because the product failed impurity specifications for a related compound.
Teva Pharmaceuticals is recalling Risedronate Sodium Delayed-release Tablets because stability testing revealed low out-of-specification dissolution results.
Metrex Research is recalling CaviWipes Extra Large surface disinfectants because they may have been contaminated during the packaging process.
LEO Pharma is recalling 272,062 tubes of Calcipotriene Cream because the label omitted a required excipient and a warning about contact dermatitis.
Merge Healthcare is recalling Merge Cardio software versions 9.0 and 10.0 because measurements from images or US carts do not transfer to reports in the correct unit of measure.
Siemens is recalling nine Biograph Mobile PET/CT systems because mobile-specific instructions were not shipped to a limited population of devices.
Merge Healthcare is recalling specific versions of Merge PACS software because studies may fail to propagate or import via the telmed protocol.
Siemens is recalling 18 Biograph 6 TruePoint mobile PET/CT systems because mobile-specific instructions were not shipped to a limited population.
Siemens is recalling four Biograph Mobile PET/CT units because specific mobile instructions were not shipped to a limited population.
Sandoz Inc is recalling specific lots of Pioglitazone and Glimepiride Tablets because they failed to meet dissolution specifications.
Siemens Healthcare Diagnostics is recalling Dimension Vista LOCI Progesterone tests because DHEA-S causes falsely elevated results.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Progesterone tests because DHEA-S causes falsely elevated results.
Siemens Medical Solutions is recalling six Biograph Mobile PET/CT units because mobile-specific instructions were not shipped to a limited population of systems.
Integra LifeSciences Corp. is recalling 39 units of the UNI-CP System due to incorrect labeling on the plate.
Navistar is recalling 2016-2018 International heavy diesel trucks because a mounting bracket may fracture, causing air leaks and increased stopping distance.
Mercedes-Benz is recalling 2016 G550 and G63 vehicles because a door cable may break, preventing occupants from opening the door from inside after a crash.