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.
Rachael's Food Corporation is recalling its Springfield Smoked Fish Lox Cream Cheese Spread due to potential Listeria monocytogenes contamination.
Rachael's Food Corporation is recalling its Smoked Fish Strawberry Cream Cheese Spread due to potential Listeria monocytogenes contamination.
Rachael's Food Corporation is recalling its Springfield Smoked Fish Spreadable Cream Cheese Spread due to potential Listeria monocytogenes contamination.
Pfizer is recalling 1,972 bottles of Zoloft 25 mg tablets because weight variations caused some tablets to be sub or super potent.
Mercedes-Benz is recalling specific 2009-2013 models because the passenger air bag inflator may explode during deployment, potentially causing serious injury or death.
Nissan is recalling 2009-2012 Versa vehicles because the passenger air bag inflator may explode during deployment, posing a risk of serious injury or death.
Rachael's Food Corporation is recalling Springfield Smoked Chubs because the product may be contaminated with Listeria monocytogenes.
Rachael's Food Corporation is recalling Smoked Trout due to potential Listeria monocytogenes contamination. Consumers should check lot numbers and discard or return the product.
Rachael's Food Corporation is recalling Springfield Smoked Fish Chunky Whitefish Spread due to potential Listeria monocytogenes contamination.
Pfizer is recalling specific lots of diphenoxylate hydrochloride and atropine sulfate tablets because weight variations caused some tablets to be sub-potent or super-potent.
KTM is recalling 2015-2018 1290 Super Duke R and GT motorcycles because a front brake piston may fail, increasing crash risk.
Smiths Medical ASD Inc. is recalling Medfusion Syringe Infusion Pumps because a loose clamp mechanism may cause the device to incorrectly alarm for invalid syringe sizes.
Figi's, Inc. is recalling specific Dark Chocolate Gingersnaps because they contain undeclared milk, a major food allergen.
Zimmer Biomet is recalling specific hip fracture stems because the internal patient label may be incorrect, although the outer box and product are correctly identified.
Zimmer Biomet is recalling specific femoral distal assemblies because the internal patient label may be incorrect, although the outer box and product are correctly identified.
Zimmer Biomet is recalling specific OSS Cemented IM Stem units because the internal patient label may be incorrect, although the outer box and product itself are correctly identified.
World Finer Foods is recalling Rapunzel Vegetable Bouillon because the front label claims no added salt, but sea salt is listed in the ingredients.
Zimmer Biomet is recalling CER BIOLOXD OPTION HD 32MM implants because the internal patient label may be incorrect, although the outer box and product are correctly identified.
Zimmer Biomet is recalling ECHO POR FMRL NC 9X125 medical devices because the internal patient label may be incorrect, although the outer box and product are correctly identified.
Zimmer Biomet is recalling a specific lot of distal femoral knee implant assemblies because the internal patient label may be incorrect, although the product itself is correctly identified.
Zimmer Biomet is recalling Lateral Troch Plate Full Crimp units because the internal patient label may be incorrect, though the product itself is correct.
Smiths Medical is recalling Medfusion Syringe Infusion Pumps because a loose clamp mechanism may cause the device to incorrectly alarm for invalid syringe sizes.
Zimmer Biomet is recalling CER OPTION TYPE 1 TPR SLEVE -6 devices because the internal patient label may be incorrect, although the outer box and product are correctly identified.
Zimmer Biomet is recalling Lateral Troch Plate Full Crimp devices because the internal patient label may be incorrect, although the outer box and product are correctly identified.
Zimmer Biomet is recalling COMP Primary Stem 8MM MINI devices because the internal patient label may be incorrect, although the product itself is correctly identified.