Kinetic Concepts, Inc KinAir MedSurg, flotation therapy, powered hospital bed, manufactured by Kinetic Concepts, Inc., San Antonio, Texas Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
KinAir MedSurg, flotation therapy, powered hospital bed, manufactured by Kinetic Concepts, Inc., San Antonio, Texas
Brand
Kinetic Concepts, Inc
Lot Codes / Batch Numbers
Serial Numbers KASK00001 through KASK01212
Products Sold
Serial Numbers KASK00001 through KASK01212
Kinetic Concepts, Inc is recalling KinAir MedSurg, flotation therapy, powered hospital bed, manufactured by Kinetic Concepts, Inc., San due to Weld failure causes side rail welds to turn upside down or break off of the bed.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Weld failure causes side rail welds to turn upside down or break off of the bed.
Recommended Action
Per FDA guidance
The firm initiated the recall by telephone on 06/06/2003. The firm has inspected and corrected the beds.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026