O-Two Medical Technologies, Inc.: Medical Device Recall in 2017 - (Recall #: Z-2705-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: June 23, 2015

Date Posted: July 19, 2017

Recall Number: Z-2705-2017

Event ID: 77528

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.

Status: Terminated

Product Quantity: 4382 units (4082 units distributed USA)

Code Information:

Lot #s: 079810; 078734, 081071, 140411, 141117, 140719, 140506, 130117 Expiration date: Jul.2016

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated