FDA Medical Device Recalls (openFDA)
Sunrise Medical, Inc.: Sunrise Hoyer Advance Patient lifts
- Recall number
- Z-0785-05
- Recalling firm
- Sunrise Medical, Inc.
- Product
- Sunrise Hoyer Advance Patient lifts
- Status
- Terminated
- Initiated
- 2005-02-03
- Posted
- 2005-05-03
- Terminated
- 2005-08-08
- Reason
- The leg actuation mechanism on certain Hoyer Advance Patient Lifts may not operate properly, which could cause the lift to become unstable.
- 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
- 27 units
- Distribution
- Domestic distribution: WI, FL, GA, TX, OK. Foreign distribution: Canada. No military or VA facilities
- Lot, serial or model codes
- Model: Hoy-Advance-E; Serial Numbers: 0409L2383, 0409L2384, 0411L001-0411L0023. Model: Hoy-Advance-H; Serial Numbers: 0409L2341-0409L2380, 0410L0680-0410L0727, 0410L0781-0410L0862.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FSA
- Firm FEI
- 1720745
- Firm city
- Longmont
- Firm state
- CO
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28