Low Flow Disposable Patient Circuit for the Precision Flow System — Class II medical device recall Z-1272-2023
Ongoing recall by Vapotherm, reported 2023-03-29, distributed nationwide. There have been reports of excessive condensation associated with certain lots of the Low Flow Disposable Pati
| Recall number | Z-1272-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Vapotherm, Exeter, NH, United States |
| Recall initiated | 2022-12-16 |
| Classified | 2023-03-17 |
| Reported by FDA | 2023-03-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | GB |
| Quantity | 5,869 total |
| UPC / GTIN / UDI-DI | 00841737104971 |
| Lot numbers | LFTL41015, LFTL41261, LFTL41262, LFTL41263, LFVLC8399, LFVLE8494, LFVLE8495, LFVLE8568, LFVLE8588, LFVMA8502, LFVMA8503, LFVMA8504, LFVMA8507, LFVMA8567, LNTL41544 |
Product
Low Flow Disposable Patient Circuit for the Precision Flow System, Product Code PF-DPC-LOW
Reason for recall
There have been reports of excessive condensation associated with certain lots of the Low Flow Disposable Patient Circuits (DPCs) used with Precision Flow System which may lead to excessive rainout.
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-1272-2023. 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.