Device recall
Z-1493-2025: Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number…
FDA device recall · Class I · Draeger, Inc.
Key facts
| Recall number (Z-number) | Z-1493-2025 |
|---|---|
| Recall event | 96342 |
| Product | 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… |
| Product code | CAI |
| Recalling firm | Draeger, Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 2517967 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database