Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 2,041–2,052 of 2,908 recalls
The impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
The impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
The impacted lots have a higher occurrence of invalid rates when compared to the product Instructions for Use.
Left Ventricular Assist System Mobile Power Unit (MPU) may have electrical component that may cause MPU not to turn on, unprompted shut down, or turning off/restarting, may cause system controller to indicate Yellow Wren…
The hip cup liner that was packaged with the incorrect labeling. HDL-060-C22S-000101 from Lot 1788258 contained a hooded liner, but it was labeled to have a standard liner.
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.