State
72,919 recalls have nationwide distribution and so reach Northern Mariana Islands. 22 additional recalls listed Northern Mariana Islands specifically in their distribution scope.
Of the 22 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 8 (36%) are Severe.
Which agencies issued them
These figures cover only the 22 recalls whose distribution notice names Northern Mariana Islands specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Prevost is recalling 2026 H3-45 and H3-45 VIP buses because aftermarket driver-side mirrors may detach, creating a road hazard.
About 211,520 MCS and Lullaby Lane one-piece footed sleepwear items sold at Meijer are being recalled because they violate the mandatory flammability standard for children's sleepwear.
About 1,770 Prismatic 3D Prints Book Nooks with Lights are being recalled because the spare lithium coin battery can be easily accessed by children.
Medline is recalling 94 units because these lots of reprocessed catheters may contain small particles of residual material.
Medline is recalling 311 units because these lots of reprocessed catheters may contain small particles of residual material.
Medline is recalling 228 units because these lots of reprocessed catheters may contain small particles of residual material.
Medline is recalling 650 units because these lots of reprocessed catheters may contain small particles of residual material.
Medline is recalling 41 reprocessed Livewire steerable diagnostic electrophysiology catheters because these lots may contain small particles of residual material.
McKesson is recalling 116 cartons of UDENYCA pegfilgrastim-cbqv injection because they were stored in a controlled room temperature environment instead of the required refrigerated environment.
Medline is recalling 511 reprocessed Siemens ACUSON AcuNav diagnostic ultrasound catheters because these lots may contain small particles of residual material.
Medline is recalling 48 reprocessed St. Jude Supreme and Response diagnostic electrophysiology catheters because these lots may contain small particles of residual material.
Asteria Health is recalling 1,699 pellets of ESTRADIOL, 18 mg sterile pellets over the potential presence of metal particulate matter.
Hologic is recalling 681,870 Brevera Breast Biopsy System disposable 9 gauge needles because particulates in affected devices can be deposited into breast tissue during use.
Medline is recalling 7,570 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Asteria Health is recalling 62,581 pellets of Testosterone, 87.5 mg sterile pellets over the potential presence of metal particulate matter.
Philips is recalling 655 units of the Azurion 7 B12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Philips is recalling 1 of the Azurion 7 B20 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Amerisource Health Services is recalling 31,676 packages of Oxycodone Hydrochloride Tablets 5 mg over card seal defects that let tablets fall out of their cavities.
Medline is recalling 4,300 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Philips is recalling 326 units of the Azurion 5 M12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Philips is recalling 922 units of the Azurion 5 M20 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Intuitive Surgical is recalling 47 da Vinci 5 Surgeon Console Viewer Displays manufactured with outdated firmware, which may cause loss of the 3D surgical field or complete visualization loss.
Philips is recalling 1 of the Azurion 7 M12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Elekta is recalling Leksell GammaPlan version 11.1 because an error when defining a new stereotactic reference may produce a treatment plan that irradiates the incorrect patient location.
Medline is recalling 21,854 units of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.