FDA Medical Device Recalls (openFDA)
Joerns Healthcare Inc.: Hoyer Hydraulic Patient Lifters model C-CB-L2, C-HLA, C-HLA-2, HML-400, C-HLA-2T and C-HLA-1. Distributed by Sunrise Medical, Inc. 7477 East Dry Creek Parkway, Longmont, CO 80503 USA.
- Recall number
- Z-0904-06
- Recalling firm
- Joerns Healthcare Inc.
- Product
- Hoyer Hydraulic Patient Lifters model C-CB-L2, C-HLA, C-HLA-2, HML-400, C-HLA-2T and C-HLA-1. Distributed by Sunrise Medical, Inc. 7477 East Dry Creek Parkway, Longmont, CO 80503 USA.
- Status
- Terminated
- Initiated
- 2006-01-06
- Posted
- 2006-05-25
- Terminated
- 2008-03-02
- Reason
- A field correction is being conducted on select models of Hoyer Patient Lifts because of hydraulic jack problems that have resulted in patient injury. The possibility exists that the mounting stud located in the bottom of the hydraulic jack could become loose allowing the jack to disengage from the mast of the lift.
- Root cause
- Other
- Action
- A Technical Service Bulletin was distributed along with an Urgent Medical Device Correction letter providing details for checking the mounting stud. UPDATE: Sunrise Medical sent a Second Notice Urgent Medical Device Correction letter, in follow-up to the January 2006 notice, to Dealer/Distributors starting 04/26/06. This Notice updates customers as to what Sunrise''s field correction will be for the Hoyer Model Hydraulic Patient Lifts. The Notice states that use of the affected devices should be discontinued until the lift has been inspected and repaired. Dealers/Distributors that have distributed the product are to notify the user to discontinue use, if possible. If the lift needs to be used then the Dealer/Distributor is to do an interim maintenance.
- Quantity
- 32,109
- Distribution
- Nationwide, Canada, Asia, South America
- Lot, serial or model codes
- Devices manufactured between July 1, 2001 and December 31, 2004. Model & Serial Number (S/N) Range: C-CB-L2 (S/N''s 0301L0905) , C-HLA (S/N''s: 0110L001 to 0412L0176, 0110J194 to 0204J0795, 0205H0043 to 412H0080 , C-HLA-2T (S/N''s 0206L1296 to 0409L2483, 0206H0945 to 0409H2570), C-HLA-2 (S/N''s 0107L0030 to 0412L0524, 0110J0195 to 0201J1338, 0202H0586 to 412H0082), HML400 (S/N''s 0110L061 to 0412L0127, 0110J098 to 0208J0162, 0112H555 to 0409H2418).
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FSA
- Firm FEI
- 2182305
- Firm city
- Stevens Point
- Firm state
- WI
- 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