State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Snapp's Ferry Packing Company is recalling approximately 410 pounds of ground beef that may be contaminated with E. coli O157:H7.
Nestle Waters North America is recalling Sweet Leaf Organic Half and Half Lemonade Tea because the product contains glass particles.
Motor Coach Industries is recalling specific MCI buses because missing welds on driver seat brackets could allow seat belt anchors to separate, increasing injury risk in a crash.
Ortho-Clinical Diagnostics is recalling VITROS 5600 Chemistry Systems due to a software anomaly that may cause erroneous test results without user notification.
Nestle Waters North America is recalling Sweet Leaf Organic Original Sweet Tea because the product contains glass particles.
CompView Medical is recalling 10 NuCARTGN mobile display units because the spring arm may detach if the securing ring was not installed correctly.
Altec is recalling 2010-2015 AH75, AH85, and AH100 aerial devices because a hydraulic valve may allow unexpected movement, increasing injury risk.
Cheryl & Co. is recalling Jingle Bell ornaments sold by QVC because sharp metal edges on the cutouts pose a laceration hazard.
Nestle Waters North America is recalling Sweet Leaf Organic Tea Mint & Honey because the product contains glass particles.
Nestle Waters North America is recalling Sweet Leaf All Natural Peach Iced Tea because the product contains glass particles.
Brainlab AG is recalling RT Elements software because large objects may display cropped during import, potentially affecting radiation treatment planning.
Ortho-Clinical Diagnostics is recalling VITROS 3600 Chemistry Systems due to a software anomaly that may allow the device to process assays at incorrect temperatures, potentially producing erroneous results.
Intuitive Surgical is correcting the da Vinci Xi I&A User Manual to prevent unintended patient harm from capacitive coupling when using 8mm endoscopes with specific instruments.
GMAX Helmet LLC is recalling specific GM78 Fullface helmets that may not adequately protect users in a crash. Owners can exchange the helmet or receive a refund.
Intuitive Surgical is correcting the da Vinci Xi I&A User Manual to warn about unintended patient harm from capacitive coupling when using 8 mm endoscopes with specific instruments.
Freedom Pharmaceuticals is recalling specific lots of Domperidone API for prescription compounding due to potential cross-contamination with penicillin.
Ortho-Clinical Diagnostics is recalling VITROS 5,1 FS Chemistry Systems because a software anomaly may cause the device to process assays at incorrect temperatures, potentially producing erroneous results.
Nestle Waters North America is recalling Sweet Leaf Organic Raspberry Iced Tea because the product contains glass particles.
Setra is recalling 2011-2012 S407CC and S417TC buses because missing welds on seat brackets could cause seat belts to detach during a crash.
Nestle Waters North America is recalling Sweet Leaf All Natural Citrus Green Tea because the product contains glass particles.
Bayer Healthcare is recalling Medrad Source Administration Sets because tubing defects may cause incorrect dose positioning during nuclear medicine procedures.
Mercury Medical is recalling Neo-Tee T-Piece Resuscitators and circuits because incorrect use can cause complete circuit occlusion, leading to failure to ventilate the patient.
Ortho-Clinical Diagnostics is recalling VITROS 4600 Chemistry Systems because a software anomaly may cause the device to process assays at incorrect temperatures, potentially producing erroneous results.
Amerisource Health Services is recalling specific lots of Hydrochlorothiazide capsules because they contain particulate matter.
ArthroCare Corporation is recalling 262 Cavity 8 Gauge Spine Wands because cracking in the tray compromises the sterile barrier.