FDA Enforcement Class I Ongoing

Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex EPA Model/Catalog Number: MP17103 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended for single use only

Recall: Z-1499-2025 · Reported April 9, 2025

Enforcement

Recall Number
Z-1499-2025
Event ID
96342
Classification
Class I
Status
Ongoing
Product Type
Devices
Firm
Draeger, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
April 9, 2025
Initiation Date
March 12, 2025
Classification Date
April 3, 2025
Address
3135 Quarry Rd, Telford, PA, 18969-1042, United States

Description

Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex EPA Model/Catalog Number: MP17103 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended for single use only

Reason

The potential for cracks forming in the breathing circuit hose.

Code Info

Model/Catalog Number: MP17103; UDI Number 04048675695660; All lot numbers.

Distribution

Domestic: Nationwide Distribution. International - following countries: Austria, Belgium, Bulgaria, China, Croatia, Czech Republic, France, Germany, Ghana, Greece, Guatemala, Hungary, India, Italy, Japan, Panama, Philippines, Portugal, Singapore, South Africa, Spain, Sweden, United Kingdom

Quantity

13620 units