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Terminated

KCI Underbed Inverter, Accessory to Powered Flotation Therapy Bed, manufactured by Kinetic Concepts, Inc., San Antonio, TX. Model number 201189

FDA Recall Z-0890-04 · Posted 2004-07-20

Recalling FirmKinetic Concepts, Inc
Recall StatusTerminated
Product CodeIOQ
Date Initiated2004-03-22
Date Terminated2005-11-02
Product Quantity33 units

Reason for Recall

Battery outgassing of powered hospital beds

Firm Action

The firm initiated the recall via letter on 03/22/2004.

Root Cause

Other

Distribution Pattern

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

Official Source

View FDA Recall →

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

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