FDA Medical Device Recalls (openFDA)
The OR Group: Stryker Universal Imaging Extension (OEM) Catalog Number: R--934-TRIO-A1
- Recall number
- Z-0183-04
- Recalling firm
- The OR Group
- Product
- Stryker Universal Imaging Extension (OEM) Catalog Number: R--934-TRIO-A1
- Status
- Terminated
- Initiated
- 2003-11-06
- Posted
- 2003-12-10
- Terminated
- 2005-07-25
- Reason
- Imaging table with extension may fail if the table leg is incorrectly positioned and the load exceeds the maximum weight of 400 lb
- Root cause
- Other
- Action
- The OR Group forwarded by 2nd day mail on 11/6/03 the repair kit and instructions to the accounts.
- Quantity
- 2 units
- Distribution
- Nationwide. CA, FL, GA, IA MI, MT, NH, OH, NJ, NY, SC, UT, TX, VA
- Lot, serial or model codes
- Serial Numbers: 217335, 214331.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FPS
- Firm FEI
- 1221538
- Firm city
- Acton
- Firm state
- MA
- 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