# FDA recall Z-1272-2023

> **Vapotherm** · Class II · device recall initiated 2022-12-16.

## 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.

## Distribution

Worldwide distribution - US Nationwide and the country of UK.

## Key facts

- **Recall number:** Z-1272-2023
- **Recalling firm:** Vapotherm
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-12-16
- **Report date:** 2023-03-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Exeter, NH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1272-2023

## Citation

> AI Analytics. FDA recall Z-1272-2023. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1272-2023. Source: US FDA. Licensed CC0.

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