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.
Hospira Inc. is recalling 30,840 bags of 0.9% Sodium Chloride Injection, USP, 100mL, due to a potential leak at the administrative port that compromises sterility.
Alere San Diego, Inc. is recalling INRatio 2 PT/INR monitors because they may provide results significantly lower than reference laboratory methods.
Winnebago is recalling specific 2013-2015 Minnie and Sunnybrook Remington travel trailers because the axle may crack the propane pipe fitting, creating a fire hazard.
DePuy Orthopaedics is recalling 1,130 I.M. Hole Locator Instruments because excessive force during use may lead to intra-operative femoral fracture.
Synthes (USA) Products LLC is recalling 12 Small Electric Drive units due to potential unintended starts or reverse mode failures that could cause tissue damage.
Nissan is recalling 2014-2015 Pathfinder, Rogue, and Infiniti QX60 vehicles because front wheel hub fasteners may be under-torqued, risking brake separation.
Siemens Medical Solutions is recalling 4,462 e.cam emission computed tomography systems due to a potential risk of patient finger injury.
KCI USA is recalling CelluTome Epidermal Harvesting System Harvesters because blades may drift and protrude from the top plate during shipping.
Centurion Medical Products is recalling 42 Chest Tube Tray kits because a single unit was found to contain human hair embedded in the stopper.
Centurion Medical Products is recalling 8 pacemaker trays because a customer reported human hair embedded in the stopper of a single unit.
Intuitive Surgical is voluntarily correcting 202 da Vinci Si Vision Side Carts where caster wheel bolts may unthread, causing wheels to loosen.
NPD Furniture is recalling about 250 Abby Dining Chairs because the legs can break unexpectedly, posing a fall hazard. No injuries have been reported.
Horiba Medical is recalling ABX PENTRA Reagent Containers because they may not sit properly in the rack, potentially causing incorrect test results without an alarm.
Vision RT Inc. is recalling 55 AlignRT 3D surface imaging systems due to a potential use error when the external Gate Controller is turned on after software startup.
Centurion Medical Products is recalling 760 Diagnostic Imaging Trays due to a confirmed report of human hair embedded in a stopper.
Baxter Healthcare is recalling HomeChoice and HomeChoice Pro Automated Peritoneal Dialysis systems because the patient guide lacks updated warnings and cautions.
Qualitest Pharmaceuticals is recalling specific lots of Acetaminophen and Codeine Phosphate Oral Solution because they failed impurity specifications for p-Aminophenol.
Aurobindo Pharma USA Inc is recalling 24,816 bottles of Gabapentin 300 mg capsules nationwide because of complaints that the capsules were empty.
Centurion Medical Products is recalling 480 Nerve Block Trays due to a confirmed report of human hair embedded in a stopper.
Siemens Healthcare Diagnostics is recalling Dimension Vista Myoglobin Calibrators because they may cause test results to shift up to 12% higher than expected.
Stryker Orthobiologics is recalling Imbibe Bone Marrow Aspiration Needles due to a potential breach in the inner or outer packaging pouches.
Par Pharmaceutical is recalling one lot of HydrALAZINE Hydrochloride tablets because small aluminum particles were found in the product.
Stryker Orthobiologics is recalling Imbibe Aliquot Needle Bone Cement Needles due to potential breaches in the inner or outer packaging pouches.
Spinal Elements is recalling Ti-Bond marketing literature because the content regarding the Ti-Bond coating is unsubstantiated and misleading for spine applications.
Baxter Healthcare is recalling 55 Amia Automated PD systems due to a battery charging error that prevents the device from functioning.