FDA Medical Device Recalls (openFDA)
Stryker Medical Div. of Stryker Corporation: Stryker Medical Stair-PRO Stair Chair with wheels, patient transport device, Model 6251.
- Recall number
- Z-0148-2010
- Recalling firm
- Stryker Medical Div. of Stryker Corporation
- Product
- Stryker Medical Stair-PRO Stair Chair with wheels, patient transport device, Model 6251.
- Status
- Terminated
- Initiated
- 2009-09-02
- Posted
- 2009-11-09
- Terminated
- 2011-02-16
- Reason
- The front of the handle may become detached from the chair, which could result in a patient fall or an operator injury.
- Root cause
- Device Design
- Action
- Consignees were sent a letter titled URGENT MEDICAL DEVICE CORRECTION dated 9/9/09, advising them of the problem and to remove the devices from service until they have been repaired. U.S. customers were notified that Stryker will complete the correction while international customers were sent a kit with instructions for completion of the correction. International consignees were told that Stryker will complete the correction if the consignee does not feel comfortable in doing so. Questions or comments regarding this issue should be addressed to Sarah Marie Puterbaugh of Stryker Medical at (800) 869-0770 ext. 6902.
- Quantity
- 65
- Distribution
- Worldwide distribution - Colorado, Ohio, Wisconsin, and Germany, Italy, Netherlands, Poland and Switzerland.
- Lot, serial or model codes
- Serial numbers 080639995, 080640003, 081039395, 080639996, 080640004, 081039396, 080639997, 080739856, 081039397, 080639998, 080739857, 081039398, 080639999, 080739858, 081039399, 080640000, 080739859, 081039400, 080640001, 080739860, 081039401, 080640002, 080740001, 081039402, 080439860, 080439861, 080439862, 080439863, 080439864, 080439865, 080439866, 080439867, 080441124, 080439868, 080541216, 080541293, 080541294, 080541295, 080541296, 080541297, 080541298, 081039403, 081039404, 081040900, 081040901, 081040902, 090139365, 090139366, 090139367, 090139368, 090139369, 090139373, 090140687, 090140691, 090140692, 090140693, 090140694, 090140688, 090140695, 090140689, 090140696, 090140690, 090241071, 090241072 and 090241073.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FPP
- 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