FDA Medical Device Recalls (openFDA)
Stryker Medical Div. of Stryker Corporation: Stryker Medical Secure II Med/Surg Bed, 230 V, Stryker Medical, Portage, MI.; Model 3221 (not sold in the U.S.).
- Recall number
- Z-1688-2008
- Recalling firm
- Stryker Medical Div. of Stryker Corporation
- Product
- Stryker Medical Secure II Med/Surg Bed, 230 V, Stryker Medical, Portage, MI.; Model 3221 (not sold in the U.S.).
- Status
- Terminated
- Initiated
- 2008-02-01
- Posted
- 2008-09-19
- Terminated
- 2010-11-05
- Reason
- The brakes may not have adequate holding power to lock the bed in place.
- Root cause
- Device Design
- Action
- Consignees were notified via letter dated 2/1/08 and informed that upgrade kits along with full written and video installation instructions will be sent to correct the problem.
- Quantity
- 66,558 of all models.
- Distribution
- Worldwide, Argentina, Brazil, Canada, Chile, China, Greece, India Japan, Mexico, Poland, Singapore, South Africa, South Korea, Switzerland, Taiwan and United Kingdom.
- Lot, serial or model codes
- Serial numbers 040915077 through 071116347.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FNL
- Firm FEI
- 1831750
- Firm city
- Portage
- 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