State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
BMW is recalling 2019 X5 xDrive40i and xDrive50i vehicles because the sun visors may lack required air bag warning labels, increasing injury risk in crashes.
Mercedes-Benz is recalling 2018-2019 GLA 250 vehicles because sunroof bonding may allow water leaks that could prevent the window air bag from deploying.
Manhattan Toy is recalling 'Find the Bear' soft books because a metal grommet can detach, posing a choking hazard to young children.
GE Healthcare is recalling 6,458 B20i patient monitors worldwide because network configuration issues may cause the devices to restart unexpectedly.
Heartware, Inc. is recalling 2,031 HVAD System Battery Charger units because they were manufactured with incorrect inductors. The recall covers units distributed in the US and multiple international countries.
Schwan's is recalling Sea Salt Caramel Cashew Ice Cream due to potential glass contamination. Consumers should check production codes and stop using the product.
Nissan is recalling 2015-2017 Altima vehicles because a rear door latch-lock cable may interfere with the window regulator, causing the door to open unexpectedly.
GE Healthcare is recalling 6,864 B40i patient monitors worldwide because network configuration issues may cause the devices to restart unexpectedly.
Howmedica Osteonics Corp. is recalling 28,461 Tritanium Posterior Lumbar cage implants because of reports of fractures occurring during or after surgery.
Dennis Eagle is recalling 2017-2018 Elite refuse trucks because the reverse alarm mute switch can prevent the vehicle from beeping in reverse, increasing injury risk.
GE Healthcare is recalling 33,065 PROCARE B40 patient monitors because network configuration issues may cause the devices to restart unexpectedly.
Mercedes-Benz is recalling 2018 S-Class and AMG S63 vehicles because an incorrect steering boot installation may keep the Active Steering Assist system engaged while the driver's hands are off the wheel.
Mercedes-Benz is recalling 2,364 2018 C300 and C300 4MATIC vehicles because improperly adjusted headlights may reduce driver visibility and increase crash risk.
Mercedes-Benz is recalling 2019 CLS 450 and AMG CLS53 vehicles because unsealed headlight adjustment screws may cause improper alignment, increasing crash risk.
Toyota is recalling 2019 Tundra trucks with spray-in bed liners because incorrect load capacity labels may lead to overloading and increased crash risk.
GE Healthcare is recalling 28,004 PROCARE B20 patient monitors because network configuration issues may cause the devices to restart unexpectedly.
GE Healthcare is recalling 5,516 B105/125 patient monitors worldwide because network configuration issues may cause the devices to restart unexpectedly.
GNC is recalling Women's Iron Complete supplements because the blister packaging is not child-resistant, posing a risk of poisoning to children.
St. Jude Medical is recalling Deep Brain Stimulation leads where the most proximal unsegmented electrode may be made of MP35N instead of the required 90/10 platinum-iridium.
4Patriots, LLC is recalling Chicken a la King pouches because milk is not declared on the label. The product was sold nationwide in emergency kits.
Porsche is recalling 2017-2018 Panamera vehicles because a software failure may cause intermittent loss of electric power steering assist, increasing crash risk.
GE Healthcare is recalling 103 LOGIQ E10 Ultrasound Systems because a trans-esophageal probe may overheat, posing a risk of burn injury to patients.
Seagrave is recalling 2017-2018 Capital and Marauder II emergency vehicles because Whelen accessory brake lights may falsely illuminate, increasing crash risk.
CAO Group, Inc. is recalling fas.TRACT Coagulative Hemostatic Gel kits due to current Good Manufacturing Practice (cGMP) violations identified during a recent inspection.
Tosoh Bioscience is recalling AIA-900 and AIA-2000 analyzers due to a potential incubator slippage issue that may cause system errors and delays in patient test results.