FDA Medical Device Recalls (openFDA)
Stryker Medical Div. of Stryker Corporation: Stryker Renaissance Series/Advantage Series PACU wheeled stretcher, Model 1509, Stryker Medical, Portage, MI 49002
- Recall number
- Z-0236-2008
- Recalling firm
- Stryker Medical Div. of Stryker Corporation
- Product
- Stryker Renaissance Series/Advantage Series PACU wheeled stretcher, Model 1509, Stryker Medical, Portage, MI 49002
- Status
- Terminated
- Initiated
- 2004-11-15
- Posted
- 2007-11-10
- Terminated
- 2010-10-27
- Reason
- The brake cams may crack or develop excessive wear, resulting in the brakes not locking the wheels, or the stretcher not being locked firmly in position.
- Root cause
- Component change control
- Action
- The firm issued an Urgent Medical Device Correction Letter dated 9/24/07, to each consignee informing them of the problems, that the brakes on each affected stretcher needed to be inspected/tested and removed from service if brake problems were discovered, and that a Stryker service representative would be in contact to replace the brakes.
- Quantity
- 81,367 (61,708 U.S. and 19,569 ex-U.S.) for all models.
- Distribution
- Worldwide-USA, Argentina, Australia, Brazil, Canada, Chile, China, Dubai, France, India, Italy, Japan, Germany, Greece, Hong Kong, Korea, Latin America, Malaysia, Mexico, Netherlands, Poland, Portugal, Singapore, South Africa, Spain, Sweden, Switzerland, Taiwan, and United Kingdom.
- Lot, serial or model codes
- All stretchers with serial numbers beginning with 0309 through 0505.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FPO
- 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