State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
KIND, LLC is recalling several varieties of KIND and Strong & KIND bars due to the potential presence of peanut protein.
Hot Mama's Foods is recalling Trader Joe's Edamame Hummus due to possible Listeria monocytogenes contamination.
Hot Mama's Foods is recalling approximately 14,860 pounds of hummus and dip products due to concerns about possible Listeria monocytogenes.
Hot Mama's Foods is recalling approximately 14,860 pounds of hummus and dip products due to concerns about possible Listeria monocytogenes.
Hot Mama's Foods is recalling Archer Farms Traditional Hummus due to concerns about possible Listeria monocytogenes contamination.
Medical Supply Liquidators LLC is recalling Vitamin B12 Methylcobalamin 5000 Injection USP because the manufacturer is not registered with the FDA.
Alexion Pharmaceuticals is recalling 96,506 vials of Soliris (eculizumab) because the product failed appearance tests for visible particles under labeled storage conditions.
Janssen Pharmaceuticals is recalling one lot of Risperdal CONSTA (risperidone) 25 mg dose packs due to a sterility failure detected in a stability sample.
Hot Mama's Foods is recalling approximately 14,860 pounds of hummus and dip products due to concerns about possible Listeria monocytogenes contamination.
Medical Supply Liquidators LLC is recalling Vitamin B6 Pyridoxine HCL for Injection because the manufacturer is not FDA-registered and the product lacks an approved NDA/ANDA.
General Motors is recalling 2011-2014 Chevrolet Express and GMC Savana CNG vehicles due to a potential natural gas leak that could cause a fire or explosion.
Forest River is recalling 2012-2015 Coachmen Prism motor homes because improper welds may allow the propane tank to fall off, increasing fire risk.
KIND, LLC is recalling several Strong & Kind and Kind protein bars nationwide and in Mexico due to the potential presence of peanut protein.
The FDA is recalling G.A.C. 375 Injection USP because the manufacturing firm is not registered with the FDA as a drug manufacturer.
Medical Supply Liquidators LLC is recalling Vitamin B12 Hydroxocobalamin Injection vials because the manufacturer is not FDA-registered and the product lacks an approved NDA/ANDA.
Medical Supply Liquidators LLC is recalling L-Carnitine Injection USP 100 mg/ml because it was marketed without an approved NDA/ANDA and the manufacturer is not registered with the FDA.
Medical Supply Liquidators LLC is recalling B Complex for Injection USP with Methylcobalamin because it was marketed without an approved NDA/ANDA and the manufacturer is not FDA-registered.
KIND, LLC is recalling several KIND and Strong & KIND bar varieties due to the potential presence of peanut protein.
Medical Supply Liquidators LLC is recalling BCAA 4% Branched Chain Amino Acid Injection USP because it was marketed without an approved NDA/ANDA and the manufacturer is not FDA-registered.
KIND, LLC is recalling several protein bar varieties nationwide and in Mexico due to the potential presence of peanut protein.
KIND, LLC is recalling specific lots of KIND Healthy Grains Maple Pumpkin Seed Bars and other bars due to the potential presence of undeclared peanut protein.
Medical Supply Liquidators LLC is recalling Super MIC B Complex injections because the manufacturer is not FDA-registered and the product lacks an approved NDA/ANDA.
Medical Supply Liquidators LLC is recalling Lipo 8 Injection USP 200 mg/ml vials because the manufacturer is not registered with the FDA and the product lacks an approved NDA/ANDA.
PJ's Truck Bodies is recalling 2009-2013 Ford F-350, F-450, and F-550 trucks modified with specific PTO assemblies due to an oil leak that poses a fire risk.
Carestream Health is recalling KODAK DirectView DR 9000 systems because a control failure may cause the U-Arm to move downward unexpectedly at three times the normal speed.