State
73,566 recalls have nationwide distribution and so reach Delaware. 3,438 additional recalls listed Delaware specifically in their distribution scope.
Of the 3,438 recalls naming Delaware we have scored against our rubric, 477 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,110 (32%) are Severe.
Which agencies issued them
These figures cover only the 3,438 recalls whose distribution notice names Delaware specifically. The 73,566 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 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.
Daimler Trucks is recalling 2021-2022 Thomas Built school buses due to loose tie rod clamps that could cause steering failure. Approximately 479 vehicles are affected.
Bard Peripheral Vascular Inc. is recalling 2,194 PowerPort duo M.R.I. Implantable Ports due to potential catheter flushing, infusion, and aspiration difficulties, as well as septum dislodgement.
ICU Medical is recalling Spiros transfer sets due to a molding defect that may cause leakage in the inactivated position.
Keystone is recalling certain 2021 Montana High Country trailers because 120VAC wiring connectors for the slide room circuit were not mounted properly. Water can enter the electrical connections, increasing the risk of fire.
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 administration sets because a molding defect may cause leakage in the inactivated position.
ICU Medical is recalling Spiros Closed Male Luer devices due to a molding defect that may cause leakage in the inactivated position.