FDA Medical Device Recalls (openFDA)
Stryker Medical: Stryker brand Synergy extended stay stretcher; model 1050
- Recall number
- Z-0304-04
- Recalling firm
- Stryker Medical
- Product
- Stryker brand Synergy extended stay stretcher; model 1050
- Status
- Terminated
- Initiated
- 2003-12-30
- Posted
- 2004-07-20
- Terminated
- 2004-04-15
- Reason
- Users may be pinched in the siderail assembly when raising or lowering the siderail.
- Root cause
- Other
- Action
- Customers were sent a recall letter dated December 30, 2003. The firm will visit each facility and modify the siderail assembly.
- Quantity
- 107
- Distribution
- United States and Colombia.
- Lot, serial or model codes
- All units.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- INK
- Firm FEI
- 1831750
- Firm city
- Kalamazoo
- Firm state
- MI
- 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