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.
Hospira Inc. is recalling Labetalol Hydrochloride Injection due to the presence of particulate matter, including metal embedded in glass vials and visible particles in the solution.
Boehringer Ingelheim Roxane Inc. is recalling 5,364 bottles of Calcitriol Oral Solution 1 mcg/mL due to a failed impurity specification.
Cooper Tire is recalling specific Wild Country Radial XTX Sport tires manufactured in June 2014 due to sidewall cracking that increases the risk of blowouts and vehicle crashes.
Hospira is recalling 142,152 bags of Heparin Sodium in 5% Dextrose Injection due to a confirmed report of fluid leaking from the primary container, which compromises sterility.
Fresenius Kabi USA, LLC is recalling Fosphenytoin Sodium Injection vials due to potential glass delamination and particulates.
Koru Pacific Packaging is recalling Ah! Laska Organic Cocoa Non Dairy Chocolate Mix because internal testing found milk allergen in the product.
Fresenius Kabi USA, LLC is recalling 728,880 vials of Fosphenytoin Sodium Injection due to potential glass delamination and particulates.
Zimmer, Inc. is recalling 852 units of M/L Taper Reduced Neck hip joint prostheses because black residue was observed in the sterile pouches.
B. Braun Medical is recalling 10,835 Stopcock Extension Sets because some stopcocks are assembled in reverse, causing them to close when set to open.
RGI Medical is recalling 19,200 units of Henora 300psi I.V. Catheter Extension Sets due to a defect that may cause the tubing to separate from the luer connection during use.
Bazzini Holdings is recalling Barricini Milk Chocolate Peanut Butter Pretzels because some containers have incorrect labels that fail to declare wheat.
Ricon is recalling specific wheelchair lift models because the platform side plate may crack, potentially causing the platform to fall and injure the operator.
3M is recalling Attest Auto-readers because labels failed to disclose dry natural rubber content, posing an allergy risk.
Trans National Trading is recalling 486 Outlaw T-70 XL motorcycle helmets manufactured in August 2012 because they fail to comply with federal safety standards.
Hospira is recalling 13 units of MedNet MMS software due to a defect that may fail to send specific dosing units to infusion pumps.
Tiffin is recalling 2014 Allegro Bus vehicles because seat belts may fray and fail to restrain occupants in a crash.
Steris Corporation is recalling 3,689 STERIS 4085 General Surgical Tables because a defective pressure switch may cause the hand control to incorrectly indicate that floor lock feet are locked.
Tiffin is recalling 2013 Allegro Bus vehicles because seat belts may be incorrectly attached and fray, reducing their strength and increasing injury risk in a crash.
Nantucket Distributing is recalling resin wicker outdoor patio set chairs because the rear legs can break, posing a fall hazard. No injuries have been reported.
Zimmer, Inc. is recalling M/L Taper Hip Prostheses with Kinectiv Technology because black residue was observed in the sterile pouches.
Karl Storz Endoscopy is recalling 968 Essential NEO audio/visual integration units because the connected power cable could overheat, generate smoke, and cause the peripheral to stop working.
Cenorin is recalling 25 HLD System Model 610 units because a temperature sensor defect may prevent water from heating during pasteurization.
The FDA is recalling 264 Devon Supine, Lithotomy and Trendelenburg Positioning Kits because straps may separate from the foam pad.
Zimmer, Inc. is recalling M/L Taper Hip Stems because black residue was observed in the sterile pouches. The recall covers 1,487 units distributed worldwide.
Zimmer Manufacturing B.V. is recalling 496 bone screws because two lots were commingled and packaged with incorrect labels.