Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1,321–1,332 of 2,908 recalls
When fenestrated analysis with clock measurements is started in diagnostic bioimaging software (intended to measure/visualize cardiovascular structures) and the 12h position of a single clock is changed, other clock meas…
High pressure tubing may relax over time causing it to partially separate from the connector resulting in a void that can trap air in the line.…
High pressure tubing may relax over time causing it to partially separate from the connector resulting in a void that can trap air in the line.…
High pressure tubing may relax over time causing it to partially separate from the connector resulting in a void that can trap air in the line.…
High pressure tubing may relax over time causing it to partially separate from the connector resulting in a void that can trap air in the line.…
Potential for Bartels ELISA Legionella Urinary Antigen kit B1029-440 lot 065 and 066 to contain particulate matter.
Due to misaligned V-Lock feature on the Mobile Power Unit power cords, which prevents the locking mechanism from properly engaging with the Mobile Power Unit and may cause unintended disconnect.
Due to misaligned V-Lock feature on the Mobile Power Unit power cords, which prevents the locking mechanism from properly engaging with the Mobile Power Unit and may cause unintended disconnect.
Inconsistent size terminology and color coding used on labeling
Inconsistent size terminology and color coding used on labeling
Due to manufacturing issue, neurostimulator device may experience "cable disconnect" error message and interruption to stimulation output.
Knee implants contain incorrect labeling (size and/or side incorrect)