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.
AbbVie is recalling 12 kits of Lupron Depot-Ped due to a potentially defective needle stick protection device.
Medtronic is recalling Activa neurostimulators because current labeling indicates the cycling feature improves device longevity and recharge interval.
AbbVie is recalling 2,915 Lupron Depot kits because the syringe needle protection device may be defective. The recall covers nationwide distribution and Puerto Rico.
Integra LifeSciences is recalling CUSA Excel Disposable Wrenches because some units were incorrectly assembled with the wrong hex wrench insert.
AbbVie is recalling 7,362 Lupron Depot kits because some may contain a syringe with a defective needle stick protection device.
Caraco Pharmaceutical Laboratories is recalling 91,777 bottles of Venlafaxine Hydrochloride Extended-Release Tablets, 37.5 mg, because stability results showed the product did not meet drug release dissolution specifications.
Medtronic is recalling specific neurostimulators because current labeling indicates the cycling feature improves device longevity, a claim that may be inaccurate.
Teva Pharmaceuticals is recalling Fluoxetine Capsules due to a customer complaint trend regarding capsule odor, indicating chemical contamination.
Legacy Pharmaceutical Packaging is recalling 667,068 bottles of Fluoxetine Capsules, 20 mg, due to supplier complaints of unusual odor.
P&L Developments is recalling 1,363,338 bottles of Children's Triacting Night Time Cold & Cough with PE because small amounts of diphenhydramine and mannitol precipitated out of solution.
AbbVie is recalling 1,530 Lupron Depot kits because some may contain a syringe with a defective needle stick protection device.
Aaron Industries is recalling 108,792 bottles of Tussin DM cough syrup because a white substance, identified as the active ingredient Guaifenesin, was observed in some bottles.
Apotex Inc. is recalling Risperidone Oral Solution because it failed impurity specifications at the 18-month stability time point.
Genesis Pharmaceuticals is recalling 461 bottles of Glytone Acne Treatment Facial Cleanser due to out-of-specification viscosity results.
Caraco Pharmaceutical Laboratories is recalling specific lots of Cetirizine Hydrochloride Chewable Tablets because they failed impurity testing.
Keystone RV is recalling 2014 Dutchmen Infinity fifth wheel trailers because interior steps may fracture, posing a fall and injury risk.
Cycling Sports Group is recalling about 80 2014 Cannondale tandem bicycles because the fork can break, causing riders to lose control and potentially be injured.
Federal Coach is recalling 2010 Spirit and Premier buses because voltage spikes may damage door actuator circuit boards, increasing the risk of fire.
Nissan is recalling 2014 Pathfinder, Rogue, and Infiniti QX60 vehicles because a right-side lug nut may not be properly tightened, posing a wheel separation risk.
HME, Inc. is recalling one 2013 Ferrara Intruder Ember emergency vehicle because the seat belt latch plate can become partially engaged, making it difficult to unlatch.
Trans Tech Bus is recalling 2013 SC139DSFP500 school buses equipped with specific Ricon wheelchair lifts. An armored cable may not clear the lift, potentially causing a short circuit and fire.
Mobility is recalling 2013-2014 modified Ford E-150 and E-250 buses because a wheelchair lift cable may cause a short circuit and fire.
Coach and Equipment is recalling 2013 Metro Lite and Phoenix buses because a wheelchair lift cable may cause a short circuit and fire.
Polaris is recalling specific 2014-2015 Victory motorcycles because an engine defect may cause the engine to seize, increasing the risk of a crash.
RMP Athletic Locker is recalling boys' Ripzone Hooligan hooded jackets because the neck drawstrings pose a strangulation and entanglement risk to children.