RecallDepth

Synergy Pulse, Powered Flotation Therapy bed, Model number 5609. Designed to provide enhanced static and pulsation pressure relieving therapies. Provides sixteen pressure zones for customizing the support surface to each patient, and is capable of providing pulsation therapy.

Company
Hill-Rom Manufacturing, Inc.
Recall Initiated
October 9, 2008
Posted
January 7, 2009
Terminated
December 10, 2009
Recall Number
Z-0600-2009
Quantity
2,083 units (Total for all 4 units)
Firm Location
Charleston, SC

Reason for Recall

These devices have the potential to overheat.

Distribution

Nationwide Distribution.

Lot / Code Info

All serial numbers

Root Cause

Device Design

Action Taken

All end users (those who either purchased the device and any customer that has rented) were notified by an Urgent Field Safety Notice on/about 10/31/2008. The letter informed the customers of the safety risk and list steps they can take to mitigate the risk until a Hill-Rom representative is able to modify the device. For the devices that were sold, the consignee of each device was notified by letter for the safety risk and what they can do to mitigate the risk until a Hill-Rom representative is able to modify the device. For the devices that are rented, an internal notification was sent via e-mail to Service Centers (Because the device is owned by the manufacturer, Hill-Rom, each Service Center in possession of the device will be the Consignee). Each Service Center will perform the correction on the units affected.

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