Maquet Inc Servo-i Ventilator Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Servo-i Ventilator
Brand
Maquet Inc
Lot Codes / Batch Numbers
All Servo-i units with serial numbers below 17617.
Products Sold
All Servo-i units with serial numbers below 17617.
Maquet Inc is recalling Servo-i Ventilator due to Complaints about batteries indicating a satisfying remaining time but after a short time suddenly shut off without giving alarms to indicate short rem. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Complaints about batteries indicating a satisfying remaining time but after a short time suddenly shut off without giving alarms to indicate short remaining battery back-up time. (Power off alarm will be given).
Recommended Action
Per FDA guidance
Maquet sent out a Safety alert Letter on 3/31/2005 to all users of the Servo-i.
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