FDA Medical Device Recalls (openFDA)
DeRoyal Industries Inc: DeRoyal TOTAL HIP TRACECART, REF 53-1820.14, Rx ONLY, NON-STERILE. Custom surgical kit containing Stryker CBCII Blood Conservation Kit.
- Recall number
- Z-1072-2010
- Recalling firm
- DeRoyal Industries Inc
- Product
- DeRoyal TOTAL HIP TRACECART, REF 53-1820.14, Rx ONLY, NON-STERILE. Custom surgical kit containing Stryker CBCII Blood Conservation Kit.
- Status
- Terminated
- Initiated
- 2009-12-09
- Posted
- 2010-03-11
- Terminated
- 2010-05-20
- Reason
- Custom surgical kits contain Stryker CBCII Blood Conservation Kit which may lack sterility.
- Root cause
- Nonconforming Material/Component
- Action
- DeRoyal initiated its recall by visit on 12/09/2009 and followed by letter dated 12/18/2009
- Quantity
- 119 units
- Distribution
- LA & MS
- Lot, serial or model codes
- Lot numbers: 08150012, 08156012, 08179012, 08172012, 08221012, 08207012, 08247012, 08249012, 08302012, 08270012, 08310012, 08312012, 08354012, 09022012, and 08354012
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LRO
- Firm FEI
- 1043214
- Firm city
- Powell
- Firm state
- TN
- 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