ClearanceBrief
Recall Z-1218-2015 ยท IKZ Bed, Patient Rotation, Powered

Arjo Hospital Equipment AB

TriaDyne Proventa Critical Care Therapy System. The TriaDyne Proventa Critical Care Therapy System provides a comprehensive system of pulmonary and skin care therapies for the critically ill, immobilized patient.

DateFeb 27, 2015 (initiated Dec 3, 2014)
StatusTerminated
ReasonThe recalled devices labeling and instructions for use contain unapproved medical claims.
Root causeLabeling design
ActionDevices in the rental fleet will be delivered to the customer with revised documents including the updated information. The customers who purchased the devices will be notified of the recall via letter sent by registered mail. The field correction notice will include a recall letter, response form, and updated labeling.
Quantity567 units
DistributionWorldwide Distribution. US nationwide, Germany, Austria, France, Italy, India, EU, Mexico, Switzerland, Canada, Saudi Arabia, Kuwait, Middle East, China, Japan, and Qatar.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.