MAQUET Inc. Ventilator System Servo-i V3.1 Maquet Critical Care PC1771 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Ventilator System Servo-i V3.1 Maquet Critical Care PC1771
Brand
MAQUET Inc.
Lot Codes / Batch Numbers
Article number 64-87-800---Serial Numbers 14000-22772
Products Sold
Article number 64-87-800---Serial Numbers 14000-22772
MAQUET Inc. is recalling Ventilator System Servo-i V3.1 Maquet Critical Care PC1771 due to The Connection of certain nebulizers to the built in driver has lead to reduced or no nebulization effect on the Servo-i Ventilator. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The Connection of certain nebulizers to the built in driver has lead to reduced or no nebulization effect on the Servo-i Ventilator
Recommended Action
Per FDA guidance
Maquet Critical Care issued an ''Extended Warranty'' letter on 5/23/2006. On March 13, 2007, Maquet modified its recall strategy and issued a Recall Notification letter accompanied by a Safety Alert letter to all customers with Servo-i ventilators, serial numbers in the 14000-22772 range, with Servo nebulizer installed. The Safety Alert letter provides customers with information on how to identify if the unit is affected, and how to identify if the unit has shown any failures, as well as, any precautions. Firm initiated recall is on-going
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