Teleflex Medical Hudson RCI ConchaTherm Neptune Heated Humidifier — Class II medical device recall Z-1558-2015
Terminated recall by Teleflex Medical, reported 2015-05-06, distributed nationwide. Customer complaints were received of power to the unit ceasing and the display going blank.
| Recall number | Z-1558-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Teleflex Medical, Research Triangle Park, NC, United States |
| Recall initiated | 2015-04-01 |
| Classified | 2015-04-30 |
| Reported by FDA | 2015-05-06 |
| Terminated | 2025-03-05 |
| Distributed | Nationwide (US) |
| Countries outside the US | BE, JP |
| Quantity | 7,228 units |
| Serial numbers | 611040101, 611040106, 611040107, 611040108, 611040109, 611040110, 611040111, 611040113, 611040114, 611040117, 611040118, 611040119, 611040120, 611050001, 611050002, 611050004, 611050005, 611050008, 611050010, 611050013, 611050015, 611050019, 611050021, 611050022, 611050023 and 475 more |
Product
Teleflex Medical Hudson RCI ConchaTherm Neptune Heated Humidifier, Rx Only.
Reason for recall
Customer complaints were received of power to the unit ceasing and the display going blank.
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-1558-2015. 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.