Devices

Device Recall KCI TriaDyne Proventa

Model / Serial
The following serial numbers: TDBK00029, TDBK00294, TDBK00015, TDBK00291, TDBK00026, TDBK00027, TDBK00123, TDBK00124, TDBK00125, TDBK00127, TDBK00128, TDBK00130, TDBK00132, TDBK00136
Product Classification
Physical Medicine Devices
Device Class
2
Implanted device?
No
Distribution
Product was distributed domestically in the following states: IN, CA, NH, OR, PA, TX, WI, CO, IA, KS, MO, ID, MA, NC, IL, OH, MN, AZ, NE, HI, PR, NC
Product Description
KCI TriaDyne Proventa Critial Care Therapy System, manufactured by Kinetic Concepts, Inc., San Antonio, Texas 78219. Model number 308900
Manufacturer
Kinetic Concepts, Inc
1 Event
- Recall of Device Recall KCI TriaDyne Proventa

Manufacturer

Kinetic Concepts, Inc

Manufacturer Address
Kinetic Concepts, 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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