Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit… — Class I medical device recall Z-1496-2025
Ongoing recall by Draeger, Inc., reported 2025-04-09, distributed nationwide. The potential for cracks forming in the breathing circuit hose.
| Recall number | Z-1496-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Draeger, Inc., Telford, PA, United States |
| Recall initiated | 2025-03-12 |
| Classified | 2025-04-03 |
| Reported by FDA | 2025-04-09 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, BE, BG, CN, CZ, DE, ES, FR, GB, GH, GR, GT, HR, HU, IN, IT, JP, PA, PH, PT, SE, SG, ZA |
| Quantity | 780 units |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 04048675389637 |
| Model numbers | MP02738 |
Product
Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 2 Model/Catalog Number: MP02738 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 Component: Not applicable
Reason for recall
The potential for cracks forming in the breathing circuit hose.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1496-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.