FDA Medical Device Recalls (openFDA)
Stryker Medical: Stryker brand Rugged EZ-Pro R4 Ambulance Cot, model 6092.
- Recall number
- Z-0023-05
- Recalling firm
- Stryker Medical
- Product
- Stryker brand Rugged EZ-Pro R4 Ambulance Cot, model 6092.
- Status
- Terminated
- Initiated
- 2004-08-17
- Posted
- 2004-10-20
- Terminated
- 2004-10-19
- Reason
- Locking pins may be installed backward, and cot may drop from highest to lowest position when the users are not prepared for the drop.
- Root cause
- Other
- Action
- Service representatives visited each customer, inspected the cots, and reinstalled the lock pins, if required, beginning on August 10, 2004.
- Quantity
- 15
- Distribution
- Alabama, California, Florida, Kansas, Montana, Oklahoma, Texas and Virginia.
- Lot, serial or model codes
- Serial numbers 040639739, 040639849, 040639737, 040639738, 040639675, 040639674, 040639670, 040639671, 040639672, 040639716, 040639847, 040639848, 040639935, 040639936 and 040639937.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FPO
- 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