ClearanceBrief
Recall Z-0185-06 ยท CBK Ventilator, Continuous, Facility Use

Pulmonetic Systems, Inc.

Lap Top Ventilator (LTV) Series continuous ventilator, model LTV-950. The LTV-950 ventilator is intended to provide continuous or intermittent ventilatory support for the care of individuals who require mechanical ventilation. The LTV-950 is a prescription medical device suitable for use in institutional, home and transport settings.

DateNov 23, 2005 (initiated Nov 9, 2005)
StatusTerminated
ReasonPulmonetic Systems has identified the potential of a printed circuit board malfunction, which can result in a ventilator malfunctio (e.g. Vent INOP, HW Fault, Xducer Fault) and possibly resulting in failure of the ventilator to breathe for the patient. This malfunction may occur without an accompanying audible alarm.
Root causeOther
ActionUrgent Medical Device Recall letter dated 11/09/05 is being sent via certified mail to affected customers. The letter informs customers of the issue. A Pulmonetic Systems representative will contact the customer within 72 hours to schedule a printed circuit board replacement. Customers are advised that in the interim all ventilator-dependent patients should be constantly monitored by qualified personnel to ensure that if a malfunction occurs, alternate ventilation can be provided.
Quantity51
DistributionWithin the US to AK, AZ, CA, CO, FL, GA, ID, IL, IN, LA, MI, MO, NE, NJ, NY, NV, OH, OK, OR, PA, SC, TX, UT, VA and WI. OUS to include: Belgium, Brazil, Canada, India, Italy, Korea and United Kingdom
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K002881VENTILATOR, CONTINUOUS (RESPIRATOR), MODEL LTV 1000
Pulmonetic Systems, Inc., Oct 11, 2000
K010608MODIFICATION TO LAP TOP VENTILATOR (LTV)
Pulmonetic Systems, Inc., Mar 20, 2001
K981371LTV 1000 VENTILATOR
Pulmonetic Systems, Inc., Oct 30, 1998
K984056LTV 1000
Pulmonetic Systems, Inc., Apr 12, 1999