Z-0890-04

KCI Underbed Inverter, Accessory to Powered Flotation Therapy Bed, manufactured by Kinetic Concepts, Inc...

Name: Z-0890-04 KCI Underbed Inverter, Accessory to Powered Flotation Therapy Bed, manufactured by Kinetic Concepts, Inc...
Creator: Kinetic Concepts, Inc
Published: 2004-03-22
License: https://open.fda.gov/license/

KCI USA, Inc. / initiated 2004-03-22 / Terminated

FDA source

Kinetic Concepts, Inc began a recall of KCI Underbed Inverter, Accessory to Powered Flotation Therapy Bed, manufactured by Kinetic Concepts, Inc., San Antonio, TX. Model number 201189 on 2004-03-22. The reason FDA records is "Battery outgassing of powered hospital beds". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0890-04
Status: Terminated
Initiated: 2004-03-22
Posted: 2004-07-20
Terminated: 2005-11-02
Recalling firm: KCI USA, Inc.
Product: KCI Underbed Inverter, Accessory to Powered Flotation Therapy Bed, manufactured by Kinetic Concepts, Inc., San Antonio, TX. Model number 201189
Product code: IOQ Bed, Flotation Therapy, Powered
Reason for recall: Battery outgassing of powered hospital beds
FDA root cause: Other
Action: The firm initiated the recall via letter on 03/22/2004.
Quantity in commerce: 33 units
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 codes and lots: Serial numbers: IVAK00004, IVAK00023, IVAK00028, IVAK00034, IVAK00033, IVAK00032, IVAK00055, IVAK00060, IVAK00062, IVAK00063, IVAK00030, IVAK50000, IVAK00030, IVAK00035, IVAK00027, IVAK00054, IVAK00037, IVAK00041, IVAK00049, IVAK00044, IVAK00045, IVAK00046, IVAK00047, IVAK00048, IVAK00038, IVAK00039, IVAK00042, IVAK00043, IVAK00051, 000038251, 000038253, 000038295, 000038299

Product code IOQ

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)