ClearanceBrief
Recall Z-1629-2008 ยท MLR Sterilizer, Chemical

Advanced Sterilization Products

STERRAD 50 Sterilization System, Product Code 10050 Used to sterilize heat and moisture sensitive reusable medical devices.

DateAug 8, 2008 (initiated Feb 25, 2008)
StatusTerminated
ReasonOil mist filter fails allowing oil mist to be emitted into the vicinity of the sterilizer, which may result in the release of a mist, "haze," or "smoke."
Root causeDevice Design
ActionThe firm sent an Urgent Device Correction letter dated 4/23/08, notifying customers of a situation that may occur with all models of STERRAD Sterilization Systems (100S, 50, 200, NX and 100NX). As a precaution, personnel should leave the room if mist is observed and avoid returning until the mist has cleared. ASP asks that customers circulate this letter to any STERRAD system users within their facility and also to the Chief Administrative Officer, the Director of Biomedical Engineering, Director of Materials Management and the Chief of Nursing. The letter instructs customers on what to do
Quantity9,950
DistributionWorldwide Distribution -- including USA and countries of France, Germany, Italy, United Kingdom, Switzerland, Benelux, Uruguay, Venezuela, Argentina, Chile, Colombia, Ecuador, Belgium, Puerto Rico, Hong Kong, Indonesia, Mexico, Philippines, Australia, Austria, China, Greece, Ireland, Israel, Japan,
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K023290STERRAD 50 & STERRAD 100S STERILIZERS
Advanced Sterilization Products, Apr 3, 2003
K981625STERRAD 50 STERILIZER
Advanced Sterilization Products, Jan 11, 1999