Z-1411-06

Joerns Easy Care 2000, Model B784, Manual adjustable Hospital Bed

Name: Z-1411-06 Joerns Easy Care 2000, Model B784, Manual adjustable Hospital Bed
Creator: Sunrise Medical CCG, Inc.
Published: 2005-11-16
License: https://open.fda.gov/license/

Joerns Healthcare / initiated 2005-11-16 / Terminated

FDA source

Sunrise Medical CCG, Inc. began a recall of Joerns Easy Care 2000, Model B784, Manual adjustable Hospital Bed on 2005-11-16. The reason FDA records is "Malfunction- the Easy care drive system performance, controlling back and knee section angle adjustment, as well as, bed height adjustment could become non-functional". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1411-06
Status: Terminated
Initiated: 2005-11-16
Posted: 2006-08-25
Terminated: 2006-11-02
Recalling firm: Joerns Healthcare
Product: Joerns Easy Care 2000, Model B784, Manual adjustable Hospital Bed
Product code: FNJ Bed, Manual
Reason for recall: Malfunction- the Easy care drive system performance, controlling back and knee section angle adjustment, as well as, bed height adjustment could become non-functional .
FDA root cause: Other
Action: End-user facilities were contacted by Sunrise Medical Customer Service Team via telephone. All beds were inspected and corrected by factory-trained representatives or by affected locations'' facility engineers.
Quantity in commerce: 510
Distribution: Nationwide distribution -including states of AZ, CA, CO, FL, IA, KY, MA, MO, MS, NC, ND, OH, OK, SC, TN, TX, VA, WI, and WV.
Product codes and lots: Serial numbers: 100104, 100604, 101804, 101904, 102004, 102204, 102504, 102604, 102704, 102904, 120804

Product code FNJ

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)