ClearanceBrief
Recall Z-0325-2008 ยท M

Mini-Mitter Company, Inc.

Actical with Step, Part Number 198-0302-00, Mini Mitter, a Respironics Company, Bend, Oregon

DateJan 17, 2008 (initiated Jun 27, 2007)
StatusTerminated
ReasonCommunication Failure: the devices have a memory chip that has a limited number of read/write cycles which can trigger set up information and/or subject information anomalies or intermittent communication annomalies. If left unaddressed, the issues can lead to permanent communication failure.
Root causeSoftware design
ActionA Voluntary Medical Device Recall letter dated June 26, 2007. The recall letter will instruct the customers to 1) fill out a business reply form to confirm contact information and devices serial numbers in their possession. Then FAX this info back immediately to Stericycle or Mini-Mitter. 2) Refer to the work scheduled rework date reserved for them and noted in their recall notification letter and return the device for service at that time; and 3) Package the device appropriately, insure it and return it via UPS using the provided UPS shipping label. Product returned to Mini-Mitter will be qu
Quantity403
DistributionWorldwide
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K060919ACTICAL
Respironics, Inc., Sep 22, 2006