FDA Device

Seattle PAP Plus, MP02260

Hazard

Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.

What You Should Do

Remedy

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.

Products

Seattle PAP Plus, MP02260
Brand
Draeger Medical, Inc.
UPC
UDI-DI: 04048675548904; All lots distributed prior to 03/20/2023 (lots other than 0367.2702.13).

Units Affected

32,050 untis