Draeger Medical, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0692-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Emergency Transport Ventilator Oxylog 3000 Ventilator and Oxylog 3000 plus Ventilator Catalog Numbers: 2M86300/2M86965 and 5704813/5704831. Volume controlled and pressure-controlled emergency and transport ventilators.

Product Classification:

Class I

Date Initiated: December 22, 2015

Date Posted: February 10, 2016

Recall Number: Z-0692-2016

Event ID: 72914

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.

Status: Terminated

Product Quantity: 402 units (314 - Oxylog 3000; 88 - Oxylog 3000 Plus)

Code Information:

All Oxylog 3000 Ventilators and Oxylog 3000 Plus Ventilators with the identified catalog numbers distributed between April 2007 - December 2015.

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated