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O-Two Medical Technologies, Inc.: Medical Device Recalls in 2017

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by O-Two Medical Technologies, Inc. in 2017. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.
See this for other years:
2017
2018
2019
  • Burn Relief¿, MODEL #(s): 06BK1221, 06BK1232, 06BK1201, 06BK1200, CATALOG #(s): 06BK1221, 06BK1232, 06BK1201, 06BK1200 --- DRESSING,WOUND,HYDROGEL W/OUT DRUG AND/OR BIOLOGIC. --- Burn Relief¿ products are self-cooling, non-adhering and are intended to be used on 1st and 2nd degree burns.
  • 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
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