FDA Medical Device Recalls (openFDA)
Centurion Medical Products: Centurion Medical Products Port access tray DT7780, Sterile.
- Recall number
- Z-1076-2011
- Recalling firm
- Centurion Medical Products
- Product
- Centurion Medical Products Port access tray DT7780, Sterile.
- Status
- Terminated
- Initiated
- 2010-06-02
- Posted
- 2011-02-09
- Terminated
- 2011-02-09
- Reason
- The kits contain heparin lock flush solution USP code 504505 that is under recall by APP Pharmaceuticals. APP Pharmaceuticals is recalling the heparin because of incomplete documentation associated with test results.
- Root cause
- Nonconforming Material/Component
- Action
- Centurion Medical Products sent out Urgent Product Recall Notices on 6/3/2010. A second recall notice was sent to nonresponding consignees on 6/21/2010. The letter instructed the consignees to quarantine the recalled product and contact Centurion so that the recalled product can be retrieved.
- Quantity
- 120
- Distribution
- Nationwide distribution.
- Lot, serial or model codes
- 2009102250.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- LRS
- Firm FEI
- 1824619
- Firm city
- Howell
- 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