State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ameritrail is recalling specific 2011 Ranch King trailers because a defective hydraulic pump component may cause a loss of braking ability, increasing the risk of a crash.
Tactical Vehicle Outfitters is recalling modified 2010-2014 Ford F-350 and F-550 trucks because oil leaks from the PTO pressure switch may ignite the exhaust thermal blanket.
Health Matters America Inc. is recalling Organic Traditions Dark Chocolate Sacha Inchi Seeds because the product contains undeclared milk, a major food allergen.
Lea Industries is recalling Covington and Hannah Collection bunk beds because incorrect assembly can create a space that traps young children.
Physio-Control is recalling 96,611 LIFEPAK 1000 defibrillators because a software malfunction can cause the device to shut down unexpectedly, potentially failing to deliver a life-saving shock.
phil&teds is recalling Travel System 26 infant car seat adaptors because they can crack and break, posing a fall hazard to infants.
Abbott is recalling ARCHITECT Intact PTH Controls because a performance shift may cause falsely elevated results on patient samples.
Mercola Group is voluntarily recalling Dr. Mercola Organic Cocoa Cassava bars because they may contain undeclared milk protein.
Van Hool is recalling 2014-2015 TX40 and TX45 motorcoaches because the driver seat belt may not be properly secured, increasing injury risk in a crash.
Abbott Laboratories is recalling 7,780 kits of ARCHITECT Intact PTH Calibrators because a performance shift may cause falsely elevated patient results.
Mirka Abrasives is recalling specific 5-inch and 6-inch compact electric random orbital sanders because they can short circuit, posing a fire hazard.
Siemens Healthcare Diagnostics is recalling 40,266 ADVIA Centaur Systems VitD Total 100 test kits because samples containing fluorescein may interfere with the assay results.
Sandoz, Inc. is recalling Cefpodoxime Proxetil tablets because they contain stainless steel particles. The recall covers 22,818 bottles distributed nationwide.
Synthes, Inc. is recalling specific lots of ProDisc-C 2.0mm Milling Bits because they have an increased potential to break during use.
Beaver-Visitec International Inc. is recalling Visitec Anterior Chamber Cannulas because some units contain a sharp tip needle instead of a blunt tip cannula.
Siemens Medical Solutions is recalling nine Linear Accelerator units because they may be used with unvalidated stereotactic accessories.
Siemens is recalling ADVIA Centaur TSH3 Ultra reagent kits because samples containing fluorescein may interfere with test results.
B. Braun Medical is recalling 24-gauge Sprotte Spinal Needles and Trays because the accompanying introducer needles are missing.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Systems TSH3 Ultra kits because fluorescein samples may interfere with test results.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Systems VitD 100 test kits because fluorescein samples may interfere with assay results.
GE Healthcare is recalling 297 Centricity PACS Workstations because a software defect may cause images from previously displayed studies to be rejected unintentionally.
Siemens is recalling ADVIA Centaur VitD 500 test kits because fluorescein samples may interfere with assay results.
Siemens Healthcare Diagnostics is recalling 16,302 ADVIA Centaur BRAHMS PCT 100 test kits because samples containing fluorescein may interfere with assay results.
Siemens is recalling 177 ACUSON SC2000 ultrasound systems due to a software issue in the Stress Echo feature that may require studies to be repeated.
Wockhardt USA LLC is recalling 8,712 bottles of Metoprolol Succinate Extended-Release Tablets, 100 mg, because they failed dissolution testing.