FDA Medical Device Recalls (openFDA)
Stryker Medical Div. of Stryker Corporation: Stryker Power-PRO Powered Ambulance Cot, Model 6500.
- Recall number
- Z-1513-06
- Recalling firm
- Stryker Medical Div. of Stryker Corporation
- Product
- Stryker Power-PRO Powered Ambulance Cot, Model 6500.
- Status
- Terminated
- Initiated
- 2006-08-29
- Posted
- 2006-09-22
- Terminated
- 2007-04-18
- Reason
- The head section wheel assembly may flex outward from the cot because the head section wheel bolts, which hold the assembly upright, may back out.
- Root cause
- Other
- Action
- Consignees were notified of the recall via letter dated 8/29/06. Included with the letter were replacement bolts for each cot and installation instructions, but the customer was given the option of contacting the recalling firm for installation.
- Quantity
- 1,841 cots (44 foreign)
- Distribution
- Worldwide distribution ---- including USA and countries of Canada, China, Germany and Switzerland.
- Lot, serial or model codes
- All units with a serial number lower than 060739380. (units manufactured between 1 Oct 2005 and 15 July 2006)
- 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