Devices

Device Recall KCI RotoProne Critical Care Therapy

Model / Serial
Serial numbers: RRFK0036-RRFK00047; RRFK00049-RRFK00115; RRFK00117-RRFK00128; RRFK00141-RRFK00211; RRFK00213-RRFK00233; RRFK00235; RRFK00237-RRRFK00254; RRFK00256-RRFK00261; RRFK00263-RRFK00267; RRFK00269-RRFK00270; RRFK00273-RRFK00280; RRFK00282-RRFK00284; RRFK00287-RRFK00290; and RRJK00002.
Product Classification
Physical Medicine Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - USA and Kuwait.
Product Description
KCI RotoProne Critical Care Therapy System buckles for securing patient to the surface during proning therapy, Model 209500. || Indicated for treatment and prevention of pulmonary complications.
Manufacturer
KCI USA, Inc.
1 Event
- Recall of Device Recall KCI RotoProne Critical Care Therapy

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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