AVID Medical, Inc. recalls CT DAVINCI. Medical convenience kit.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1,381–1,392 of 2,908 recalls
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits, causing discoloration.
Due to software issue, Radiation Therapy Planning system may provide incorrect dataset calculations when performing the "Stopping Power Ratio" (SPR) ,
Control kits contain incorrect standard deviation (SD) values for the low and high control beads which compromises the accurate calculation of bead counts.
Control kits contain incorrect standard deviation (SD) values for the low and high control beads which compromises the accurate calculation of bead counts.
Laryngoscope handles may not illuminate as intended.
Laryngoscope handles may not illuminate as intended.
Laryngoscope handles may not illuminate as intended.
Laryngoscope handles may not illuminate as intended.
Laryngoscope handles may not illuminate as intended.
Laryngoscope handles may not illuminate as intended.