State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Rabbit Creek Products Inc. is recalling Paddy's Pub Classic Beer Bread Mix because it may contain flour contaminated with E. coli O121.
Rabbit Creek Products Inc. is recalling Million Dollar Brownie Mix because it may contain flour contaminated with E. coli O121. Consumers should stop using the product.
Rabbit Creek Products is recalling Flower Pot Parmesan Southwest Beer Bread Mix because it may contain flour contaminated with E. coli O121.
Rabbit Creek Products Inc. is recalling Caramel Pecan with Streusel Topping Quick Bread Mix because it may contain flour contaminated with E. coli O121.
Rabbit Creek Products Inc. is recalling Raspberry with Cabernet Wine Brownie Mix because it may contain flour contaminated with E. coli O121.
Rabbit Creek Products is recalling Redneck Brownie Mix because it may contain flour contaminated with E. coli O121.
Siemens is recalling 37 Ysio Max radiographic systems because a table part may detach, causing the table to tilt and potentially injure patients.
Ford is recalling 2017 Lincoln Continental vehicles because incorrect headlight lenses may reduce turn signal visibility, increasing crash risk.
Integra LifeSciences Corp. is recalling specific lots of Integra Drainage Accessory Kits because a final inspection found an incomplete packaging seal, potentially compromising sterility.
Forest River is recalling 2016-2017 Coachmen Galleria recreational vehicles because the cargo capacity placard is inaccurate, which may lead to overloading.
ShowHauler is recalling 2014-2015 Garage Coaches because lift gate roller chains may fail, causing the platform to drop and increasing injury risk.
Siemens is recalling 37 Multix Fusion X-ray systems because an internal table part may detach, causing the table to tilt and potentially injure patients.
RaySearch is recalling RayStation software versions 2.5 through 5.0 due to dose calculation errors when using specific region of interest settings.
Integra LifeSciences Corp. is recalling 10 units of Straight Ventricular Catheters due to an incomplete packaging seal discovered during final inspection.
Integra LifeSciences Corp. is recalling 14 units of the Ventricular Catheter Accessory Kit due to an incomplete sterile packaging seal discovered during final inspection.
Siemens Healthcare Diagnostics is recalling Dimension Vista Calcium reagent cartridges that may produce inaccurate test results.
Siemens is recalling 37 Multix Fusion VA10 radiographic systems because a table part may detach, causing the table to tilt and potentially injure patients.
Microgenics Corporation is recalling the Thermo Scientific QMS Everolimus Assay because a reagent stability issue causes inaccurate test results for transplant patients.
Mamas & Papas is recalling Armadillo Flip and Flip XT strollers because a loose latch can cause the seat to tip back, posing a fall hazard to infants.
Forest River is recalling 2017 Flagstaff and Rockwood trailers because excess slack in air conditioner wiring may contact heating elements, increasing fire risk.
Panoramic Rental Corp. is voluntarily correcting PC-1000 X-ray systems because a safety nut may be ineffective, posing a risk of blunt force trauma to the head, neck, or shoulders.
Keystone RV is recalling 84 model year 2017 Dutchmen Coleman recreational trailers because loose or frayed wiring in the power center may increase the risk of a fire.
Teva North America is recalling Claravis (isotretinoin) capsules because they failed impurity and degradation specifications.
Ivoclar Vivadent is recalling 17 units of Zenostar MT Color A3.5 dental porcelain coloring liquid due to potential packaging leaks that may cause skin irritation.
Integra LifeSciences is recalling 9 units of CUSA Dissectron Fingertip Laparoscopic Cannulas due to incomplete sterile packaging seals discovered during final inspection.