FDA Device recall Z-2706-2014
Vapotherm Precision Flow,Disposable Patient Circuit PF-NODPC-Low
- FDA Device
- Class II
- terminated
- Published 2014-10-01
On 2014-10-01 the FDA classified a Class II recall of Vapotherm Precision Flow,Disposable Patient Circuit PF-NODPC-Low by Vapotherm, citing water may leak into the center gas lumen of the Patient Circuit.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2706-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-08-13 |
| Published | 2014-10-01 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Vapotherm |
| Distribution | US |
Product
Vapotherm Precision Flow,Disposable Patient Circuit PF-NODPC-Low. For use with the Precision Flow system and Ikaria INOmax DSIR ¿ System. This DPC allows clinicians to administer nitric oxide non-invasively via high flow nasal cannula. In the Precision Flow High Flow Therapy application, a special disposable patient circuit re-routes the gas to the INOmax injector module then back into the Precision Flow system
Reason
Water may leak into the center gas lumen of the Patient Circuit
Identifiers
| code_info | Lot Numbers 1402021 through 1406010, excluding lots 1402024 through 1402028 and 1404003. These numbers are applicable r…Lot Numbers 1402021 through 1406010, excluding lots 1402024 through 1402028 and 1404003. These numbers are applicable regardless of the prefix preceding them (i.e. HF, HFE, HFH, HFN, LF, LFE, LFH or LFN). |
|---|
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-2706-2014%22
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