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.
HVL, LLC is recalling 278 bottles of Melatonin Control-Released Tablets that contained a vegetarian digestive enzyme instead of melatonin.
Teleflex Medical is recalling Aquapak 640 SW humidifier adaptors because packages may contain foreign material, specifically black particles.
Natus Medical is recalling EPWorks software versions prior to 6.0 used in the Xltek Protektor Stimulator. A software error prevents remote users from stopping free run waveform groups.
Arthrosurface, Inc. is recalling 138 Taper Post Fixation Components because they were not cleared for marketing in the US with current indications.
Arthrosurface, Inc. is recalling 182 units of Athrosurface Taper Post Fixation Components because they were not cleared for marketing in the US with current indications.
Sun Pharma Global Fze is recalling 3,263 bottles of Levetiracetam extended release tablets because they failed to meet dissolution specifications at the 6-month time point.
Teleflex Medical is recalling 2,640 units of LMA Supreme (New Cuff) Size 5 devices because some may be mislabeled as Size 5 but are actually Size 4.
Arthrosurface, Inc. is recalling 187 units of the HHXL (OVO) 15.6x32mm Taper Post Fixation Component because the product was not cleared for marketing in the US with its current indications.
Natus Medical is recalling EPWorks software versions prior to 6.0 because a software error prevents remote users from stopping free run waveform groups.
Arrow International Inc. is recalling 63,022 units of ARROW Epidural Needle Components because the product labeling does not specify the 5-year shelf life.
Lacrimedics Inc is recalling VisiPlugST devices because moisture levels may cause the plugs to break apart or crumble upon contact.
Stryker is recalling Flyte Togas with an incorrect expiration date. The label reads 2412-12-01 instead of 2014-12-01.
Chrysler is recalling 2015 Chrysler 200 vehicles because the automatic transmission parking pawl may fail to engage, increasing the risk of the vehicle rolling away.
Kia is recalling 2016 Sorento vehicles because an improperly soldered component may prevent acceleration, increasing crash risk.
Mercedes-Benz is recalling 2013-2015 E-Class and CLS-Class vehicles because a rubber seal may fall into the engine bay and contact the exhaust system, increasing fire risk.
Suomy is recalling specific Apex-S1R-EX motorcycle helmets that may not meet federal safety standards for penetration resistance, increasing injury risk in crashes.
Johnson Controls is recalling Recaro bus driver seats where a tether bar may interfere with the seat belt locking mechanism, increasing injury risk in crashes.
Scott USA is recalling 2015 Vanish Evo bicycle helmets because they do not meet CPSC impact safety standards. Consumers should stop using them and seek a refund.
Airtex is recalling specific fuel pump modules because an improper seal may cause fuel leaks, increasing the risk of a fire.
Jackco Transnational is recalling ZETA Pocket Jump Starters because the battery packs can overheat and catch fire. Consumers should stop using the product and contact the company for a refund.
SRAM is recalling Zipp 88 aluminum bicycle wheel hubs because the front hub flange ring can fail, posing a crash and injury hazard.
KTM North America is recalling 2015 KTM and Husqvarna Enduro motorcycles because front fork pistons can stick, causing loss of control and crashes.
Kidde is recalling 4.6 million disposable fire extinguishers in the U.S. because a faulty plastic valve may prevent them from fully discharging during a fire.
Siemens Medical Solutions is recalling 310 LINAC Accelerators because the internal electric board may overheat, causing thermal damage and smoke emission.
Navistar is recalling 6,302 model year 2015-2016 IC CE school buses because the powertrain wiring harness may contact a high-pressure fuel line, potentially causing a fuel leak and fire.