Z-0016-2007

Joerns Ultra Care 770 Model AC Powered Beds with model numbers U770, U770 AL , U770 GNDAL. Sunrise Medical...

Name: Z-0016-2007 Joerns Ultra Care 770 Model AC Powered Beds with model numbers U770, U770 AL , U770 GNDAL. Sunrise Medical...
Creator: Sunrise Medical CCG, Inc.
Published: 2006-01-01
License: https://open.fda.gov/license/

Joerns Healthcare / initiated 2006-01-01 / Terminated

FDA source

Sunrise Medical CCG, Inc. began a recall of Joerns Ultra Care 770 Model AC Powered Beds with model numbers U770, U770 AL , U770 GNDAL. Sunrise Medical, Long Term Care Division, 5001 Joerns Drive, Stevens... on 2006-01-01. The reason FDA records is "The control box used in the actuator systems appears to have a potential to become stuck in one position resulting a non-functioning bed". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0016-2007
Status: Terminated
Initiated: 2006-01-01
Posted: 2006-10-05
Terminated: 2007-04-09
Recalling firm: Joerns Healthcare
Product: Joerns Ultra Care 770 Model AC Powered Beds with model numbers U770, U770 AL , U770 GNDAL. Sunrise Medical, Long Term Care Division, 5001 Joerns Drive, Stevens Point, WI 54481 USA.
Product code: FNL Bed, Ac-Powered Adjustable Hospital
Reason for recall: The control box used in the actuator systems appears to have a potential to become stuck in one position resulting a non-functioning bed.
FDA root cause: Other
Action: The objective is to replace all of these systems. Phone contact of affected facilities began in January 2006. All facilities to be contacted by June 23, 2006. All products will be corrected at the location of the end-user by June 30, 2006.
Quantity in commerce: 6,921
Distribution: Nationwide and Canada.
Product codes and lots: Model U 770, serial number range: 6149310001 - 6149310005, 6151360001 - 6151360005, 6163290001 - 616330001. Model U770 AL, serial number range: 6099280001 - 6113410042, 6114760001 - 6127920006, 6128720001 - 6130360001, 6130510001 - 6135430002, 6136650001 - 6140860005, 6142190001 - 6142320001, 6142380001 - 6148440006, 6149320001 - 6151270004, 6152090001 - 6160890005, 6161480001 - 6162420010, 6163330001 - 6168440002, 6169170001 - 6171470001, 6171750001 - 6174080020, 6174750001 - 6177310002. U770-GNDAL, serial number range: 6113510001 - 6113510004, 6127970001 - 61279700015, 6130370001 - 6130370003, 6135440001, 6140870001 - 61408700010, 6142330001, 6160900001 - 61609000010, 6168450001 - 6168450004, 6171700001 - 6171720002, 6174710001 - 61747100012.

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)