ClearanceBrief
Recall Z-0653-05 ยท GWQ Full-Montage Standard Electroencephalograph

Compumedics Usa, Ltd

Nonin Xpod Oximeter model numbers 3011 and 3012, distributed for use with the Compumedics E-Series Digital Amplifier.

DateMar 24, 2005 (initiated Feb 24, 2005)
StatusTerminated
ReasonUnder specific conditions, the housing of the pulse oximeter contected to the amplifier can become excessively warm causing a burn upon contact with skin.
Root causeOther
ActionThe firm initiated the recall on February 24, 2005 via letter with return response post card.
Quantity1376 units
DistributionProduct was distributed nationwide and to the following foreign countries: Australia, Canada, Greece, Hong Kong, Hungary, India, Iran, Israel, Italy, Japan, Malaysia, Netherlands, New Zealand, Pillippines, Portugal, Saudi Arabia, Singapore, South Africa, Spain, Switzerland, Taiwan, Thailand, Turkey,
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.