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FDA Medical Device Recalls (openFDA)

Terumo Cardiovascular Systems Corp: Terumo Advanced Perfusion System 1; 220V -240V, 7A (circuit breaker), 50/60 Hz (10A power source required); Model 801764. (Not distributed within the United States).

Recall number
Z-0315-2007
Recalling firm
Terumo Cardiovascular Systems Corp
Product
Terumo Advanced Perfusion System 1; 220V -240V, 7A (circuit breaker), 50/60 Hz (10A power source required); Model 801764. (Not distributed within the United States).
Status
Terminated
Initiated
2004-05-01
Posted
2006-12-27
Terminated
2009-07-14
Reason
The gas system may fail calibration prior to use due to incorrect gas system flowmeter software.
Root cause
Process control
Action
U.S. consignees were visited and corrections made between May 2004 and November 2005. Foreign affiliates were instructed to make corrections on international units, but the firm has not received confirmation yet that these units have been corrected.
Quantity
5
Distribution
Worldwide distribution, including USA, Belgium, Germany, Japan, Korea and Republic of China.
Lot, serial or model codes
Serial numbers 0040 through 0044.
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

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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

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