FDA Medical Device Recalls (openFDA)
Stryker Medical: Stryker brand Model 1550 Synergy Extended Stay Stretcher
- Recall number
- Z-0267-04
- Recalling firm
- Stryker Medical
- Product
- Stryker brand Model 1550 Synergy Extended Stay Stretcher
- Status
- Terminated
- Initiated
- 2003-12-01
- Posted
- 2003-12-24
- Terminated
- 2004-04-12
- Reason
- The user may be pinched by the siderail when raising or lowering the siderail.
- Root cause
- Other
- Action
- Recall letters dated 12/1/03 were sent to each consignee notifying them that Stryker would be contacting them to modify the siderail assembly.
- Quantity
- 3903
- Distribution
- United States, Canada, Hong Kong, Israel, Mexico and Syria.
- Lot, serial or model codes
- All stretchers manufactured between 1/1/1993 and 11/07/2003.
- 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