FDA Device recall Z-1497-2025
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 6 Model/Catalog Number: MP02744 Software Version: Not applicab…
- FDA Device
- Class I
- ongoing
- Published 2025-04-09
On 2025-04-09 the FDA classified a Class I recall of Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 6 Model/Catalog Number: MP02744 Software Version: Not applicab… by Draeger, citing the potential for cracks forming in the breathing circuit hose.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1497-2025 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2025-03-12 |
| Published | 2025-04-09 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Draeger |
| Distribution | US |
Product
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 6 Model/Catalog Number: MP02744 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.
Identifiers
| code_info | Model/Catalog Number: MP02744; UDI Number 040486775389675; All lot numbers. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1497-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.