State
73,566 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 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Baxter Healthcare is recalling 9,353 SIGMA Spectrum Infusion Pumps due to a potential software error during programming.
Boston Scientific is recalling 419 Five IceSphere Prostate Cryoablation Kits nationwide due to a complaint trend regarding needle shaft gas leaks.
Baxter Healthcare is recalling 140,006 SIGMA Spectrum Infusion Pumps due to a potential software error during programming.
Boston Scientific is recalling 772 IceRod 1.5 MRI Cryoablation Needles nationwide due to a complaint trend regarding needle shaft gas leaks.
Biomet is recalling 21 units of Vanguard 360 Revision System Posterior Augments because tibial bolts were packaged instead of femoral bolts, which may delay knee arthroplasty procedures.
Integra LifeSciences is recalling 17 Bactiseal Endoscopic Ventricular Catheters due to mislabeling. The devices were incorrectly identified as a different catheter model.
GA Health Company Limited is recalling 50 units of Andorate Disposable Endoscope Valves because the suction button may be sticky or broken, potentially prolonging procedures.
Siemens Healthcare Diagnostics is recalling Atellica GGT Reagent because it may show repeatability imprecision outside performance data on some analyzers.
Baxter Healthcare is recalling SIGMA Spectrum Infusion Pumps due to a potential software error during programming.
Boston Scientific is recalling 211 IceSeed Prostate Cryoablation Kits nationwide due to a complaint trend regarding needle shaft gas leaks.
Fresenius Kabi is recalling 4,411 trays of Sensorcaine (Bupivacaine HCl and Epinephrine) because the epinephrine component tested below specification.
Baxter Healthcare is recalling Spectrum IQ Infusion Systems with Dose IQ Safety Software due to a potential software error during programming.
Integra LifeSciences is recalling 85 units of Bactiseal Ventricular Catheters that were mislabeled as Endoscopic Ventricular Catheters. The error involves swapped product labels for part numbers 823073 and 823087.
Boston Scientific Corporation recalled 525 IceEDGE cryoablation needles due to reported gas leaks in the needle shaft, affecting nationwide distribution.
Biocomposites, Ltd. is recalling 54 boxes of Stimulan Kit 10cc, Model 600-010, because the product is mislabeled. The recall affects units distributed in the US, Puerto Rico, and Costa Rica.
Applied Medical Technology Inc is recalling specific lots of ENFit-to-Stepped Male adapters because the inner pouches may have incorrect labels, although the outer boxes are correct.
Autosales Inc. is recalling Summit Racing 6-Ton Jack Stands because the ratchet bar may fail, allowing the vehicle to fall. Owners should stop using the stands and contact Autosales for a refund.
Yamaha is recalling 2016-2020 FJR1300 motorcycles because a transmission gear can crack and break, potentially locking the rear wheel and causing a crash.
Yamaha is recalling motorcycles for a front brake switch defect that can keep the brake light on or cause unexpected cruise control shutoff, increasing crash risk. Contact Yamaha customer service at 1-800-962-7926 for a free replacement.
Marion Body Works is recalling 2020 Spartan Gladiator and MetroStar vehicles because LCD displays may lock up, potentially delaying emergency efforts.
AvKare Inc. is recalling 14,368 bottles of Trazodone Hydrochloride Tablets 100 mg because they were inadvertently packaged with sildenafil.
Synthes (USA) Products LLC is recalling DePuy Synthes 15.5mm Reamer Heads for RIA 2 due to breakage exceeding expected rates, which can cause tissue and bone damage.
Zydus Pharmaceuticals is recalling 15,144 cartons of Lansoprazole 15 mg tablets because they failed to meet dissolution specifications.
Synthes (USA) Products LLC is recalling DePuy Synthes 14.0MM Reamer Heads for RIA 2 due to breakage rates exceeding expectations, which can cause tissue and bone damage.
Synthes (USA) Products LLC is recalling DePuy Synthes 10.0MM Reamer Heads for RIA 2 because breakage exceeds expected rates, causing potential tissue or bone damage.