Z-0158-06

ICCG AC-Powered Adjustable Medical Bed

Name: Z-0158-06 ICCG AC-Powered Adjustable Medical Bed
Creator: Invacare Corporation
Published: 2004-07-23
License: https://open.fda.gov/license/

Invacare GmbH / initiated 2004-07-23 / Terminated

FDA source

Invacare Corporation began a recall of ICCG AC-Powered Adjustable Medical Bed on 2004-07-23. The reason FDA records is "Component Defect. Metal Oxide Varister (MOV) component of the junction box may short circuit with the potential for device failure". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0158-06
Status: Terminated
Initiated: 2004-07-23
Posted: 2005-11-17
Terminated: 2012-04-12
Recalling firm: Invacare GmbH
Product: ICCG AC-Powered Adjustable Medical Bed
Product code: FNL Bed, Ac-Powered Adjustable Hospital
Reason for recall: Component Defect. Metal Oxide Varister (MOV) component of the junction box may short circuit with the potential for device failure.
FDA root cause: Other
Action: The manufacturer notified their distributors of the recall with telephone calls & a letter. The distributors were provided information about the recall and informed of their recall responsibilites.
Quantity in commerce: 14,343 units
Distribution: World wide
Product codes and lots: Model #''s:1102550, 026757, 720-3M-80PR, IH720-3MQS, IH720-3M, 720-3M-76PR, IH720-2M, IHSC900, 026746, SC900-80P, SC90080L, SC900-76L, 720FULL, IHMC2MFP76, IHMC2MF80, IHMC2MF76, IHMC2MFP76, IHMC3MFP80, IHMC3ZP4I6, IHMC2M3ZP41, IHMC23ZP236, IHMC3SP23, 1H3MRFR76, IH3MRFR80, IH3MR2076, IH3MR2080, IH3MR8FR76, IH3MF8FRU6, IH3MR8FR80, IH3MF8FRU. The serial numbers for the beds affected are as follows: 00Axxxxx thru 00Kxxxxx; 99Axxxxx thru 99Lxxxxx & 98Cxxxxx thru 98Lxxxxx.

Product code FNL

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)