Z-0785-05

Sunrise Hoyer Advance Patient lifts

Name: Z-0785-05 Sunrise Hoyer Advance Patient lifts
Creator: Sunrise Medical, Inc.
Published: 2005-02-03
License: https://open.fda.gov/license/

Sunrise Medical, Inc. / initiated 2005-02-03 / Terminated

FDA source

Sunrise Medical, Inc. began a recall of Sunrise Hoyer Advance Patient lifts on 2005-02-03. The reason FDA records is "The leg actuation mechanism on certain Hoyer Advance Patient Lifts may not operate properly, which could cause the lift to become unstable". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0785-05
Status: Terminated
Initiated: 2005-02-03
Posted: 2005-05-03
Terminated: 2005-08-08
Recalling firm: Sunrise Medical, Inc.
Product: Sunrise Hoyer Advance Patient lifts
Product code: FSA Lift, Patient, Non-Ac-Powered
Reason for recall: The leg actuation mechanism on certain Hoyer Advance Patient Lifts may not operate properly, which could cause the lift to become unstable.
FDA root cause: Other
Action: Telephone calls were placed to customers on 02/03/05. Urgent Medical Device Correction letters, dated 02/03/05, were also sent to customers.
Quantity in commerce: 27 units
Distribution: Domestic distribution: WI, FL, GA, TX, OK. Foreign distribution: Canada. No military or VA facilities
Product codes and lots: Model: Hoy-Advance-E; Serial Numbers: 0409L2383, 0409L2384, 0411L001-0411L0023. Model: Hoy-Advance-H; Serial Numbers: 0409L2341-0409L2380, 0410L0680-0410L0727, 0410L0781-0410L0862.

Product code FSA

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)