Z-0017-2007

Hill-Rom VersaCare Hospital Bed with optional patient pendant P3207A01 or P3207A02; model P3200

Name: Z-0017-2007 Hill-Rom VersaCare Hospital Bed with optional patient pendant P3207A01 or P3207A02; model P3200
Creator: Hill-Rom, Inc.
Published: 2006-07-27
License: https://open.fda.gov/license/

Hill-Rom Inc. / initiated 2006-07-27 / Terminated

FDA source

Hill-Rom, Inc. began a recall of Hill-Rom VersaCare Hospital Bed with optional patient pendant P3207A01 or P3207A02; model P3200 on 2006-07-27. The reason FDA records is "The patient pendant cord represents a potential trip hazard for the patient or the caregiver". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0017-2007
Status: Terminated
Initiated: 2006-07-27
Posted: 2006-10-05
Terminated: 2008-04-10
Recalling firm: Hill-Rom Inc.
Product: Hill-Rom VersaCare Hospital Bed with optional patient pendant P3207A01 or P3207A02; model P3200.
Product code: FNL Bed, Ac-Powered Adjustable Hospital
Reason for recall: The patient pendant cord represents a potential trip hazard for the patient or the caregiver.
FDA root cause: Other
Action: Consignees were notified via a letter dated 8/10/06 that included a package with installation instructions, materials and labels to modify the beds.
Quantity in commerce: 36,645
Distribution: Nationwide, Argentina, Australia, Brazil, Canada, China, Greece, Indonesia, Japan, Kuwait, Oman, Qatar, Thailand and United Arab Emirates.
Product codes and lots: All model P3200 VersaCare beds with the optional patient pendants P3207A01 or P3207A02.

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)