FDA Device recall Z-1558-2015
Teleflex Medical Hudson RCI ConchaTherm Neptune Heated Humidifier, Rx Only
- FDA Device
- Class II
- terminated
- Published 2015-05-06
On 2015-05-06 the FDA classified a Class II recall of Teleflex Medical Hudson RCI ConchaTherm Neptune Heated Humidifier, Rx Only by Teleflex Medical, citing customer complaints were received of power to the unit ceasing and the display going blank.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1558-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-04-01 |
| Published | 2015-05-06 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Teleflex Medical |
| Distribution | US |
Product
Teleflex Medical Hudson RCI ConchaTherm Neptune Heated Humidifier, Rx Only.
Reason
Customer complaints were received of power to the unit ceasing and the display going blank.
Identifiers
| code_info | Material number: 425-00, Serial numbers: 611040101, 611040106, 611040107, 611040108, 611040109, 611040110, 611040111, 6…Material number: 425-00, 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, 611050024, 611050027, 611050031, 611050032, 611050033, 611050038, 611050039, 611050040, 611050041, 611050042, 611050045, 611050047, 611050049, 611050050, 611050051, 611050052, 611050053, 611050055, 611050058, 611050059, 611050060, 611050061, 611050063, 611050064, 611050065, 611050066, 611050067, 611050068, 611050070, 611050072, 611050073, 611050074, 611050076, 611050077, 611050082, 611050084, 611050085, 611050086, 611050091, 611050094, 611050098, 611050099, 611050101, 611050103, 611050104, 611050106, 611050107, 611050109, 611050110, 611050115, 611050116, 611050119, 611050120, 611050121, 611050122, 611050125, 611050126, 611050127, 611050128, 611050129, 611050130, 611050131, 61 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1558-2015%22
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