# FDA recall Z-2705-2017

> **O-Two Medical Technologies, Inc.** · Class II · device recall initiated 2015-06-23.

## Product

O-Two Adult Ventilation Timer,  MODEL #(s): 01BM1000-CS, 01BM3201-MOTP-CS, 01BM3201-MOTL-CS, CATALOG #(s): 01BM1000 ---   INTENDED USE: The Adult Ventilation Timer is intended to guide the rescuer to provide ventilations at a rate appropriate for adult patients

## Reason for recall

Malfunction of an O-Two Adult Ventilation Timer, where the flash rate of the malfunctioning device was reported to be twice that of the rate noted on the label.

## Distribution

Worldwide Distribution - US (nationwide) Canada, Europe Denmark and Finland

## Key facts

- **Recall number:** Z-2705-2017
- **Recalling firm:** O-Two Medical Technologies, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2015-06-23
- **Report date:** 2017-07-19
- **Termination date:** 2017-09-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mississauga, Canada

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2705-2017

## Citation

> AI Analytics. FDA recall Z-2705-2017. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/Z-2705-2017. Source: US FDA. Licensed CC0.

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