Vapotherm, Inc.: Medical Device Recall in 2014 - (Recall #: Z-2706-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: August 13, 2014

Date Posted: October 1, 2014

Recall Number: Z-2706-2014

Event ID: 69116

Reason for Recall:

Water may leak into the center gas lumen of the Patient Circuit

Status: Terminated

Product Quantity: 207 units

Code Information:

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).

Distribution Pattern:

Worldwide Distribution - USA (nationwide) and Internationally to Canada, France, Swizerland, Korea, Sweden, Germany , Belgium, Spain, Mexico, Scotland, UAE, Australia, Israel, Hong Kong, Ireland, kuwait, and Italy.

Voluntary or Mandated:

Voluntary: Firm initiated