State
73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Major Pharmaceuticals is recalling Losartan Potassium 50 mg tablets because FDA testing found an impurity above acceptable levels.
Macleods Pharma USA Inc. is recalling Losartan Potassium and Hydrochlorothiazide tablets because an impurity was detected in the active ingredient.
Philips is recalling HeartStart MRx devices used with specific AC power modules that may fail, potentially causing loss of power and failure to deliver shocks.
Hamilton Medical is recalling 4,338 HAMILTON-G5 ventilators with software versions 2.60 or lower because they may enter an ambient state, requiring immediate alternative ventilation.
Golden State Medical Supply Inc. is recalling Losartan Potassium 50 mg tablets because an impurity was detected in the active ingredient.
Golden State Medical Supply is recalling Losartan Potassium 50 mg tablets because a nitrosamine impurity was detected in the active ingredient.
Macleods Pharma USA Inc. is recalling Losartan Potassium 50 mg tablets because an impurity was detected in the active ingredient.
GE Healthcare is recalling 9,094 Giraffe Infant Radiant Warmers because bedside panels and latch areas can crack or break if the unit is moved using the panels instead of the designated handles.
Teva Pharmaceuticals is recalling Losartan Potassium 100 mg tablets because an impurity was detected in the active ingredient.
Volkswagen is recalling 27,822 2015-2016 CC and Tiguan vehicles because a defective air bag control unit may cause air bags to fail or deploy unexpectedly.
Golden State Medical Supply Inc. is recalling Losartan Potassium 50 mg tablets because an impurity was detected in the active ingredient.
Applied Medical Resources Corp is recalling Kii Fios First Entry devices because they may not have met sterility requirements, potentially exposing patients to infectious agents.
Navistar is recalling 2020 IC CE school buses because an electrical overload in the Body Control Module may cause the engine to start unexpectedly, increasing injury risk during service.
Porsche is recalling 2016-2017 911, Boxster, Cayman, and Panamera vehicles because a defective capacitor in the air bag control unit may cause air bags to fail or deploy unexpectedly.
Macleods Pharma USA Inc. is recalling Losartan Potassium tablets because an impurity was detected in the active ingredient.
Bodum is recalling Bistro Toasters because they can leak electric current at maximum temperature, posing a shock hazard. No U.S. injuries were reported, but eight shocks occurred in Canada.
COVIDIEN LLC is recalling MAHURKAR and Argyle acute hemodialysis catheters because the printed priming volume values are higher than the volumes required to fill each lumen.
Canon Medical System is recalling 46 Radrex-i X-Ray Systems due to a software malfunction that prevents image transmission from the wireless flat panel detector.
Richard Wolf Medical Instruments Corp. is recalling E-Line Cutting Electrodes because some packages contain the wrong electrode type.
Rinovum Women's Health is recalling the Revive Reusable Bladder Support because the device may split or crack during its intended use life.
American Health Packaging is recalling Anastrozole Tablets due to potential cross-contamination from cleaning procedure failures.
Braun is recalling modified 2017-2020 Toyota Siennas because improperly manufactured steering shaft extensions may fracture, potentially causing loss of steering.
K2 Sports is recalling VO2 S inline skates because the axle can loosen or break, causing wheels to separate and posing a fall hazard. No injuries have been reported.
VIVO is recalling MOUNT-PLAY5 speaker wall mounts because the front ledge can loosen, causing speakers to fall. No injuries have been reported.
Epic Business Services is recalling Majestic Pure Wintergreen Oil because the packaging fails to meet child-resistant closure requirements, posing a poisoning risk to young children.