FDA Medical Device Recalls (openFDA)
Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1, 4 inch diameter Roller Pump; Model 801040.
- Recall number
- Z-0490-2007
- Recalling firm
- Terumo Cardiovascular Systems Corp
- Product
- Terumo Advanced Perfusion System 1, 4 inch diameter Roller Pump; Model 801040.
- Status
- Terminated
- Initiated
- 2006-10-16
- Posted
- 2007-02-14
- Terminated
- 2009-07-07
- Reason
- The pump may lose communication with the central control monitor, causing the monitor to display a service message "System Computer Needs Service" and to become non-operational.
- Root cause
- Other
- Action
- Consignees were notified of the problem via letter dated 11/10/06 and informed that they would be contacted to schedule a service call to install software upgrades. Installation of software upgrades began at customer locations on 10/16/06.
- Quantity
- 1,399
- Distribution
- Worldwide distribution --- including USA and countries of Australia, Belgium, Canada, China, Dominican Republic, Egypt, Germany, India, Indonesia, Japan, Malaysia, Mexico, Pakistan, Republic of China, Singapore, South Africa, South Korea, Thailand and United Arab Emirates.
- Lot, serial or model codes
- Serial numbers 0029, 0031 through 0043, 0045, 0047 through 0050, 0052, 0054, 0056 through 0059, 0064, 0067, 0068, 0070 through 0073, 0075 through 0080, 0082 through 0086, 0088 through 0111, 0113 through 0117, 0120 through 0123, 0125 through 0180, 0182 through 0191, 0194, 0195, 0197 through 0207, 0209, 0211 through 0527, 0700 through 0725, 0727, 0730 through 0878, 0880, 0881, 0883 through 0977, 0981 through 0990, 0992, 0993, 0995 through 1266, 1268 through 1528, 1539 through 1579, 2000 through 2018, 2023, 2025, 2027 through 2057 and 2072 through 2083.
- 510(k) numbers
- ["K022947"]
- PMA numbers
- not on file
- Product code
- DTQ
- Firm FEI
- 1828100
- Firm city
- Ann Arbor
- 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