ClearanceBrief
Recall Z-1493-2025 ยท CAI Circuit, Breathing (W Connector, Adaptor, Y Piece)

Draeger, Inc.

Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number: MP00355 Software Version: Not applicable Product Description: Breathing circuit for conveying breathing gases between an anesthesia machine or ventilator and adult patients. The breathing circuit is intended for single use only. Component: Not applicable

DateApr 3, 2025 (initiated Mar 12, 2025)
StatusOpen, Classified
ReasonThe potential for cracks forming in the breathing circuit hose.
Root causeUnder Investigation by firm
ActionOn March 12, 2025 URGENT MEDICAL DEVICE RECALL letters were sent to customers. Actions to be Taken When using these breathing circuits: 1. Use holders with a larger contact surface (see Figure 2 above). 2. Perform leak testing after stretching the flexible hose to the required length for the application. Please observe the products Instructions for Use (IFU) According to our records, you have received at least one of the listed breathing circuits. Please inform all potential users in your facility. If you have forwarded affected products to third parties, please also forward this Urgent Medica
Quantity65150 units
DistributionDomestic: 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
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.