State
73,584 recalls have nationwide distribution and so reach Hawaii. 2,772 additional recalls listed Hawaii specifically in their distribution scope.
Of the 2,772 recalls naming Hawaii we have scored against our rubric, 333 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 715 (26%) are Severe.
Which agencies issued them
These figures cover only the 2,772 recalls whose distribution notice names Hawaii specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Medical Action Industries is recalling 110 cases of Midline Insertion Kits because a component may have a package integrity breach.
Medical Action Industries is recalling LVAD Dressing Change Kits because a component may have a package integrity breach.
Meridian Bioscience is recalling 124 Revogene RNA Software Upgrade Kits because the FDA withdrew the Emergency Use Application after false negative results were reported.
Daimler Trucks North America is recalling certain 2021–2022 heavy-duty trucks including Freightliner and Western Star models due to potentially loose tie rod clamps. Loose or detached tie rod ends could cause steering loss and increase crash risk.
St. Jude Medical is recalling Assurity and Endurity pacemakers because a manufacturing issue with epoxy mixing may allow moisture to enter the device, potentially causing malfunction.
Meridian Bioscience is recalling 376 Revogene SARS-CoV-2 test kits because the FDA withdrew the Emergency Use Application after false negative results were reported.
Medical Action Industries is recalling 180 Injection REVIEW MAI Kits because a component may have a package integrity breach.
Medical Action Industries is recalling 129 cases of Blood Culture MAI Kits because a component may have a package integrity breach.
Medical Action Industries is recalling 205 cases of Blood Culture Kits because a component may have a package integrity breach.
St. Jude Medical is recalling 95,042 Endurity pacemakers because a manufacturing issue with epoxy may allow moisture ingress, potentially causing device malfunction.
Cheyenne Products is recalling about 795,000 Mainstay folding chairs and barstools because a weld can break, posing a fall hazard. Consumers should stop using them and contact Cheyenne for a refund.
GE Healthcare is recalling NM/CT 870 DR scanners because a specific workflow may cause a shift in CT radiation exposure range, potentially requiring patient re-scans.
Atos Medical AB is recalling Provox Life Night HME devices because they may be incorrectly inserted, potentially blocking the patient's stoma.
ICU Medical is recalling specific lots of Spinning Spiros Closed Male Luers because a molding defect may cause leakage in the inactivated position.
Bard Peripheral Vascular Inc. is recalling 287 PowerPort duo M.R.I. Implantable Ports due to catheter flushing difficulties and septum dislodgement.
ICU Medical is recalling specific lots of Oncology Kits with Spinning Spiros due to a molding defect that may cause leakage in the inactivated position.
GE Healthcare is recalling NM/CT 850 scanners because a specific workflow may cause a 5cm shift in CT radiation exposure, potentially requiring patient re-scans.
ICU Medical is recalling specific lots of Sprios male luer administration sets due to a molding defect that may cause leakage in the inactivated position.
ICU Medical is recalling specific lots of Sprios IV adapters because a molding defect may cause leakage in the inactivated position.
Navistar is recalling 2019-2021 IC Bus RE School Buses because a sealing washer may not seat correctly, causing the high-pressure fuel rail to leak and increasing fire risk.
IKEA is recalling HEROISK and TALRIKA bowls, plates, and mugs made of PLA material because they can become brittle and break, causing hot contents to leak and burn consumers.
Bard Peripheral Vascular Inc is recalling 189 units of PowerPort duo MRI Implantable Ports due to potential catheter flushing difficulties and septum dislodgement.
ICU Medical is recalling Spiros male luer extensions due to a molding defect that may cause leakage in the inactivated position.
GE Healthcare is recalling NM/CT 860 scanners because a specific protocol may cause a 5cm shift in radiation exposure, potentially requiring patient re-scans.
ROi CPS LLC is recalling 272 Regard Dressing Change Trays because ChloraPrep applicators in the kits can grow organisms that breach package integrity.