FDA Medical Device Recalls (openFDA)
Stryker Medical Div. of Stryker Corporation: Stryker Medical transport stretcher, Stryker Medical, Portage, MI; Model 736. Wheeled hospital stretcher.
- Recall number
- Z-0284-2010
- Recalling firm
- Stryker Medical Div. of Stryker Corporation
- Product
- Stryker Medical transport stretcher, Stryker Medical, Portage, MI; Model 736. Wheeled hospital stretcher.
- Status
- Terminated
- Initiated
- 2009-08-10
- Posted
- 2009-11-17
- Terminated
- 2010-10-29
- Reason
- The brake/steer pedal may seize, resulting in the brakes not working.
- Root cause
- Nonconforming Material/Component
- Action
- Consignees were notified by letter dated August 10, 2009 that Stryker will contact them to upgrade the stretchers within 6 months. The recall was expanded in scope to include additional serial numbers by a second letter dated September 17, 2009, which was issued to additional consignees who had not been previously notified of the recall, as well as the consignees who had been issued the August 10, 2009 letter.
- Quantity
- 75
- Distribution
- Nationwide, Argentina, Australia, Brazil, Canada, Chile, China, France, Germany, Greece, India, Italy, Japan, Korea, Latin America, Malaysia, Mexico, Netherlands, Philippines, Poland, Portugal, Singapore, South Africa, Spain, Switzerland, Taiwan, and United Kingdom,
- Lot, serial or model codes
- Serial numbers 0804104196, 0804104197, 0804105786, 0804105787, 0805101727, 0805101728, 0805101737, 0805101738, 0805102800, 0806099970, 0806101731, 0806101732, 0806102605, 0806102606, 0806102607, 0806102608, 0806102666, 0806102667, 0806102668, 0806102669, 0806102670, 0806102671, 0806102720, 0806102721, 0806102722, 0806102723, 0806102724, 0806102725, 0806104550, 0807100090, 0807100091, 0807100092, 0807100093, 0807102509, 0807102510, 0807102574, 0807102575, 0807102576, 0807102577, 0807102578, 0807102579, 0807107180, 0807107181, 0807107182, 0807107183, 0807107251, 0807107252, 0807107253, 0807107254, 0807107255, 0807108211, 0807108212, 0807108213, 0807108214, 0807108215, 0807108216, 0808104326, 0808104327, 0901032632, 0901032633, 0901034021, 0901034022, 0901034023, 0901034024, 0901034025, 0901034026, 0901034027, 0901034028, 0901034029, 0901034030, 0901034031, 0901034032, 0903033740, 0903033741 and 0903033742.
- 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
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
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