Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1,873–1,884 of 2,908 recalls
An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use.
An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use.
An issue with a raw material used to coat some surgical needles that may result in diminished performance and/or removal of some silicone needle coating during use.
Potential for the presence of visible foreign matter.
Potential for DC Power Supply housing to become hot to the touch and deform the plastic housing.
A cybersecurity vulnerability was discovered through internal testing.
A cybersecurity vulnerability was discovered through internal testing.
Adapters may disconnect during setup or while in use, potentially interrupting ventilation. Any disconnection can result in severe consequences for neonates, including hypoxia, hypercapnia, and organ failure.
Adapters may disconnect during setup or while in use, potentially interrupting ventilation. Any disconnection can result in severe consequences for neonates, including hypoxia, hypercapnia, and organ failure.
An issue was identified with the software when using the Echo Module of ISCV, the issue may result in missing or incomplete information in the report.
Potential for exoskeleton to lose lateral balance and cause patient to fall.
A software bug in Blueprint version 4.2.1 prevents users from accessing cases initiated in previous versions of the software.