ID Circuit Basic — Class I medical device recall Z-1446-2023
Terminated recall by Draeger Medical, Inc., reported 2023-05-24, distributed nationwide. Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial
| Recall number | Z-1446-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Draeger Medical, Inc., Telford, PA, United States |
| Recall initiated | 2023-04-17 |
| Classified | 2023-05-17 |
| Reported by FDA | 2023-05-24 |
| Terminated | 2024-09-03 |
| Distributed | Nationwide (US) |
| Quantity | 25 units |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 04048675421870 |
Product
ID Circuit Basic (P) 180, MP01340
Reason for recall
Glued connections of the breathing circuit can become loose before or during ventilation resulting in partial or complete detachment of pieces.
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-1446-2023. 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.