MAQUET Inc. Ventilator System SERVO-i V3.1 PC1777 Maquet Critical Care Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Ventilator System SERVO-i V3.1 PC1777 Maquet Critical Care
Brand
MAQUET Inc.
Lot Codes / Batch Numbers
Article # 64-87-800 Serial numbers 02400 - 03300
Products Sold
Article # 64-87-800 Serial numbers 02400 - 03300
MAQUET Inc. is recalling Ventilator System SERVO-i V3.1 PC1777 Maquet Critical Care due to Reported failures of the SERVO-i ventilators user interface system causing technical errors and increased fault frequencies. Switches may be activat. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Reported failures of the SERVO-i ventilators user interface system causing technical errors and increased fault frequencies. Switches may be activated unintentionally, or a function not activate when the switch is selected. Direct access knobs may not function or change the parameter in the wrong direction compared to how they are turned.
Recommended Action
Per FDA guidance
Maquet sent an ''Extended Warranty'' letter on May 23, 2006. On March 13, 2007, Maquet issued a Recall Notification letter to all customers stating that they will replace all PC1777 boards in the serial number range 2400-3300, which have not previously been replaced. A safety alert letter was included outlining the failure indication and effect for the user of the failures, as well as, how to identify whether the Servo-i unit has shown any failure indications.
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