Device recall
Z-1495-2025: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 1…
FDA device recall · Class I · Draeger, Inc.
Key facts
| Recall number (Z-number) | Z-1495-2025 |
|---|---|
| Recall event | 96342 |
| Product | Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 1 Model/Catalog Number: MP02737 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… |
| Product code | OFP |
| 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
- 10–99 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