Draeger Medical, Inc. VentStar Anesthesia (N) 180, MP00333 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
VentStar Anesthesia (N) 180, MP00333
Brand
Draeger Medical, Inc.
Lot Codes / Batch Numbers
UDI-DI: 04048675422198, All lots.
Products Sold
UDI-DI: 04048675422198; All lots.
Draeger Medical, Inc. is recalling VentStar Anesthesia (N) 180, MP00333 due to Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
Recommended Action
Per FDA guidance
The firm distributed recall notifications to consignees via FedEx starting on 4/17/2023. Consignees are instructed to immediately stop use of affected devices, inspect current stock, and quarantine any affected devices to prevent use. Alternative therapy for patients should be instituted as soon as possible and ensure all users of affected devices within consignee organizations are aware of the recall, with copies being forwarded if devices were further distributed. To replace or return unused products, consignees are to call Draeger Customer Success between 8:00 AM - 6:00 PM EST, Monday thru Friday, at 1-800-437-2437 (option 2, then option 1), or via email at US-Medical@draeger.com. A Return Materials Authorization and pre-paid shipping label will be provided upon request. Any additional questions regarding the recall communication may be directed to Mr. Michael Kelhart between the hours of 8:00 AM - 4:30 PM by phone at 267-664-1131 or by email at mike.kelhart@draeger.com.
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