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.
Pure Edge Nutrition is recalling Bella Vi eXtreme ACCELERATOR capsules because they contain undeclared sibutramine and phenolphthalein.
MyNicNaxs, Inc. is recalling SlimEasy Herbs Capsules because they contain undeclared sibutramine and N-desmethylsibutramine and were marketed without an approved NDA/ANDA.
Vitality Research Labs is recalling vitaliKOR capsules because FDA sampling found undeclared vardenafil and tadalafil. The product was marketed without an approved NDA or ANDA.
Pure Edge Nutrition is recalling Bella Vi BTrim Ultimate Boost capsules because they contain undeclared sibutramine and phenolphthalein.
Pure Edge Nutrition is recalling Bella Vi INSANE Bee Pollen capsules because they contain undeclared sibutramine and phenolphthalein.
MyNicNaxs, Inc. is recalling Super Fat Burning Bomb Capsules because they contain undeclared active pharmaceutical ingredients, phenolphthalein and N-desmethylsibutramine.
MCI is recalling specific 1993-1995 and 2006-2008 motor coaches because the driveshaft may detach, potentially causing loss of steering control and increasing crash risk.
Cubist Pharmaceuticals is recalling 51,500 vials of CUBICIN (daptomycin) because a customer reported a glass shard in one vial.
General Motors is recalling specific 2014 Chevrolet Silverado and GMC Sierra trucks because optional floor mats may not be secured, potentially interfering with the accelerator pedal.
Dual-Tech is recalling 2009-2014 modified Ford F-550 trucks because oil leaks from a PTO switch may ignite the exhaust thermal blanket.
Stryker is recalling 285 sterile 3.0mm Round Fluted Bur Aggressive devices due to missing or partial notches. The defect may affect the device's compatibility with Elite Attachments.
Brooks Furniture is recalling glider rockers sold to Kaplan Early Learning because spindles can separate, posing a fall hazard. No injuries have been reported.
Alere San Diego, Inc. is recalling 373 kits of the Alere Triage D-Dimer Test (Lot W53884B) because they may generate error codes or incorrect results.
Philips is recalling IntelliVue MX40 monitors because alarms may not resume after being paused, potentially delaying clinical response.
BioDerm, Inc. is voluntarily recalling specific skin wipes used in male incontinence devices due to potential bacterial contamination from a contract manufacturer.
BioDerm, Inc. is voluntarily recalling skin-prep wipes used with external male catheters due to potential bacterial contamination.
Ivoclar Vivadent is recalling 241 Bluephase style light probes because a stock check revealed broken glass fibers between the connector and the fiber bundle.
Maquet is recalling PowerLED 700 surgical lights because plastic tabs may break, causing the ambient light module to partially detach.
Ortho-Clinical Diagnostics is recalling VITROS 4600 Chemistry Systems due to a potential for biased results when using Multiple Window codes.
Nokia is recalling travel charger kits for the Lumia 2520 tablet because loose plastic covers can expose internal components, posing an electrocution risk.
CooperSurgical is recalling 1,180 units of the Tampa Catheter because unsealed pouches may compromise the device's sterility.
BioDerm, Inc. is voluntarily recalling skin-prep wipes used with external male catheters due to potential bacterial contamination.
Philips is recalling IntellVue Info Center monitors because a software defect causes reboot loops that interrupt patient monitoring.
Stryker is recalling four sterile Zyphr Elite Round Fluted Burs because some units may have missing or partial notches, potentially affecting their use with Elite Attachments.
Stryker is recalling 41 sterile neuro drill accessories due to missing or partial notches that may affect compatibility with Elite attachments.