Devices

Device Recall RotoRest Delta Kinetic Therapy System

Model / Serial
Model Number 208030, Serial Numbers: 00157087, 00157091, 00157288, 00157375, 00157405, RRCKOO011, RRHKOO065, RRHKOO074, RRHKOO096, RRHK00109, and RRHKOO117.
Product Classification
Physical Medicine Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution including AL, CA, CO, OK and GA.
Product Description
RotoRest Delta Kinetic Therapy System || INDICATIONS: Treatment and prevention of pulmonary complications as a result of immobility, Thoracic or lumbar fracture, Cervical traction, Skeletal traction
Manufacturer
KCI USA, Inc.
1 Event
- Recall of Device Recall RotoRest Delta Kinetic Therapy System

Manufacturer

KCI USA, Inc.

Manufacturer Address
KCI USA, Inc., 4958 Stout Dr, San Antonio TX 78219-4334
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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