State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Pierce Manufacturing is recalling 2015 Saber, Enforcer, Impel, and Velocity vehicles because the rear leaf spring spacer block may crack, posing a crash risk.
Twin City Bagel, Inc. is recalling Dan's Pantry Wheat Bagels because they may contain undeclared peanuts or almonds.
Yamaha is recalling 4,900 model year 2015 motorcycles because a defective shift cam stopper may fracture, causing transmission shifting issues and increasing crash risk.
Heritage Pharmaceuticals is recalling RIFAMPIN for Injection, USP, 600 mg per vial, due to quality control concerns regarding the assurance of sterility.
Twin City Bagel, Inc. is recalling specific Cinnamon Raisin bagels because they may contain undeclared peanuts or almonds.
Twin City Bagel, Inc. is recalling plain bagels sold under multiple brand names because they may contain undeclared peanuts or almonds.
Ossur H / F is recalling LP Rotate Foot System prosthetic devices because short threads on the shock module may cause it to detach, leading to falls.
Twin City Bagel, Inc. is recalling specific brands of whole wheat bagels because they may contain undeclared peanuts or almonds.
Medtronic is recalling 151 FlexCath Select Steerable Sheaths because clinicians observed debris originating from the hemostasis valve outside of patients' bodies.
Twin City Bagel, Inc. is recalling Kroger Cinnamon Swirl Raisin Bagels because they may contain undeclared peanuts or almonds.
Heritage Pharmaceuticals is recalling Colistimethate Sodium Injection due to quality control concerns regarding sterility assurance.
Aron Streit Inc. is recalling Streit's Kids Dark Chocolate Coins because testing revealed undeclared milk, a major allergen.
Mutual Pharmaceutical is recalling Ergoloid Mesylates 1 mg tablets because they failed impurity and degradation specifications during stability testing.
Hospira is recalling 94,440 bags of 5% Dextrose Injection due to a potential leak at the administrative port that compromises sterility.
Linon Home Décor is recalling about 3,300 foldable wood patio chairs and bistro sets because they can tip over, causing falls.
CooperSurgical is recalling Infant Heel Gel Warmers and The Infant Heel Warmer because products without expiration dates have a remote potential for minor burns.
Stryker Howmedica Osteonics is recalling 2,030 Triathlon Distal Capture Assemblies because a weld may disassociate, potentially causing the trigger mechanism to become loose or disassociated.
Elekta is recalling Precise Treatment Tables because incorrect sensor installation during maintenance can cause undetected positioning errors, potentially leading to clinical mistreatment.
Synthes, Inc. is recalling 183 thumb screws for orthopedic aiming arms because incorrect raw material was used, which may lead to stress-corrosion cracking.
CooperSurgical is recalling MediChoice Infant Heel Warmers because products without expiration dates have a remote potential for minor burns.
Goya Foods is recalling Kirby Black Beans Creole Seasoning and Goya Black Bean Soup due to possible peanut contamination.
Bard Access Systems is recalling BD PosiFlush Saline Flush Syringes because some packages may have open seals, potentially compromising sterility.
Mindray is recalling 519 Passport V Monitors because the invasive blood pressure function may provide incorrect measurements.
Bard Access Systems is recalling 16,410 units of BD PosiFlush Saline Flush Syringes included in various device kits because open seals may impact product sterility.
Bard Access Systems is recalling BD PosiFlush Saline Flush Syringes included in certain catheter kits because open seals may compromise product sterility.