Z-1555-05

Clinitron At Home Air Fluidized Therapy Bed

Name: Z-1555-05 Clinitron At Home Air Fluidized Therapy Bed
Creator: Hill-Rom Manufacturing, Inc.
Published: 2005-05-20
License: https://open.fda.gov/license/

Hill-Rom Manufacturing, Inc. / initiated 2005-05-20 / Terminated

FDA source

Hill-Rom Manufacturing, Inc. began a recall of Clinitron At Home Air Fluidized Therapy Bed on 2005-05-20. The reason FDA records is "Sudden unexpected lowering of the head of the bed may occur due to failure of the had of the bed actuator". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1555-05
Status: Terminated
Initiated: 2005-05-20
Posted: 2005-09-21
Terminated: 2006-04-26
Recalling firm: Hill-Rom Manufacturing, Inc.
Product: Clinitron At Home Air Fluidized Therapy Bed
Product code: FNL Bed, Ac-Powered Adjustable Hospital
Reason for recall: Sudden unexpected lowering of the head of the bed may occur due to failure of the had of the bed actuator.
FDA root cause: Other
Action: Customer letter was hand delivered to consignees by Hill-Rom Service Technicians 05/20/2005. The affected product will be corrected by replacement of the actuator with one from an unaffected lot.
Quantity in commerce: 21 beds
Distribution: AL, FL, KY, LA, MA, NC, NY, TN, TX, VA
Product codes and lots: Serial numbers: CS102304, CS103257, CS103901, CS103902, CS103903, CS103904, CS103909, CS103911, CS103914, CS103915, CS103916, CS103917, CS103919, CS103921, CS103923, CS103924, CS103925, CS103928, CS103932, CS103933.

Product code FNL

K942184Class IIClinitron at Home Air Fluided TherapySsi Medical Services, Inc. / cleared 1995-02-07

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)