Vapotherm Precision Flow Disposable Patient Circuit Recalled for Water Leakage
Vapotherm is recalling 22,042 Precision Flow Disposable Patient Circuits because they may allow water to leak into the center gas lumen.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a medical device used for breathing support where a defect (water leakage) poses a risk of harm, but the source text does not report specific injuries or illnesses, fitting the 'High' severity criteria for risk-of-harm products without reported injury.
Plain-English summary
Vapotherm, Inc. is recalling 22,042 units of the Vapotherm Precision Flow Disposable Patient Circuit (PF-DPC-Low). The recall is due to a defect that allows water to leak into the center gas lumen of the device.
The affected product is intended to add warm moisture to breathing gases for neonate, infant, pediatric, and adult patients in hospital, sub-acute, and home settings. The recall covers lot numbers 1402021 through 1406010, excluding lots 1402024 through 1402028 and 1404003. These lot numbers apply regardless of the prefix (HF, HFE, HFH, HFN, LF, LFE, LFH, or LFN).
The product was distributed nationwide in the United States and internationally to Canada, France, Switzerland, Korea, Sweden, Germany, Belgium, Spain, Mexico, Scotland, UAE, Australia, Israel, Hong Kong, Ireland, Kuwait, and Italy. Users should stop using the affected circuits and contact Vapotherm, Inc. for instructions.
The recalled product
- Product
- Vapotherm Precision Flow,Disposable Patient Circuit PF-DPC-Low. For use with the Precision Flow system Precision Flow" is intended for use to add warm moisture to breathing gases from an external source for administration to a neonate/infant, pediatric and adult patients in th
- Manufacturer
- Vapotherm, Inc.
- Category
- Medical Device — Respiratory
- Affected units
- 22,042
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (7)
- Lot Numbers 1402021 through 1406010
- HFE
- HFH
- HFN
- LF
- LFE
- LFH or LFN).
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 8 recalled by Vapotherm, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 8 products in this recall →Related recalls
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- HighVapotherm Precision Flow Patient Circuit Recalled for Potential Water Leakage
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