Terumo Cardiovascular Systems Corp Terumo Advanced Perfusion System 1; 100V -120V, 15 A (circuit breaker), 50/60 Hz (20A power source required) base; Model 801763. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Terumo Advanced Perfusion System 1; 100V -120V, 15 A (circuit breaker), 50/60 Hz (20A power source required) base; Model 801763.
Brand
Terumo Cardiovascular Systems Corp
Lot Codes / Batch Numbers
Serial numbers 0011 through 0039 and 0041 through 0170.
Products Sold
Serial numbers 0011 through 0039 and 0041 through 0170.
Terumo Cardiovascular Systems Corp is recalling Terumo Advanced Perfusion System 1; 100V -120V, 15 A (circuit breaker), 50/60 Hz (20A power source r due to The battery status light on the front panel may not accurately reflect the actual status of the battery. The battery may contain more charge than ind. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The battery status light on the front panel may not accurately reflect the actual status of the battery. The battery may contain more charge than indicated.
Recommended Action
Per FDA guidance
U.S. consignees were visited and new software installed between May 2004 and November 2005. Currently, approximately 50% of exported units have been upgraded.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026