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Terminated

KinAir MedSurg, flotation therapy, powered hospital bed, manufactured by Kinetic Concepts, Inc., San Antonio, Texas

FDA Recall Z-0583-05 · Posted 2005-03-10

Recalling FirmKinetic Concepts, Inc
Recall StatusTerminated
Product CodeIOQ
Date Initiated2003-06-06
Date Terminated2008-04-01
Product Quantity1181 beds

Reason for Recall

Weld failure causes side rail welds to turn upside down or break off of the bed.

Firm Action

The firm initiated the recall by telephone on 06/06/2003. The firm has inspected and corrected the beds.

Root Cause

Other

Distribution Pattern

The beds were distributed nationwide and to Brazil.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K970468KT AIR BEDKinetic Concepts, Inc. · 1997-09-05

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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