Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
O-Two Adult Ventilation Timer Recalled by O-Two Medical Technologies, Inc. Due to Malfunction of an O-Two Adult Ventilation Timer, where...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact O-Two Medical Technologies, Inc. directly.
Affected Products
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
Quantity: 4382 units (4082 units distributed USA)
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About O-Two Medical Technologies, Inc.
O-Two Medical Technologies, Inc. has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report