PlainRecalls
FDA Devices Critical Class I Terminated

Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number: 5705080. Volume controlled emergency and transport ventilator with pressure support.

Reported: February 10, 2016 Initiated: December 22, 2015 #Z-0691-2016

Product Description

Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number: 5705080. Volume controlled emergency and transport ventilator with pressure support.

Reason for Recall

Drager became aware of situations where the error message "Poti unplugged" was generated causing acoustic and visual alarms, the breathing system releases pressure and the ventilation function stops operating.

Details

Recalling Firm
Draeger Medical, Inc.
Units Affected
0
Distribution
Nationwide Distribution -- including states of AR, AZ, CA, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI, WV, and WY.
Location
Telford, PA

Frequently Asked Questions

What product was recalled?
Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number: 5705080. Volume controlled emergency and transport ventilator with pressure support.. Recalled by Draeger Medical, Inc.. Units affected: 0.
Why was this product recalled?
Drager became aware of situations where the error message "Poti unplugged" was generated causing acoustic and visual alarms, the breathing system releases pressure and the ventilation function stops operating.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 10, 2016. Severity: Critical. Recall number: Z-0691-2016.