FDA Recall Terminated

MOSAIQ Oncology Information System

Recall: Z-2917-2018 · Initiated August 3, 2018

Recall

Recall Number
Z-2917-2018
Event Number
80764
Firm
Elekta, Inc.
FEI Number
1037831
Product Code
IYE
Status
Terminated
Root Cause
Unknown/Undetermined by firm
Initiated
August 3, 2018
Terminated
September 23, 2024
Address
400 Perimeter Center Ter NE, Ste 50, Atlanta, GA, 30346-1227

Description

MOSAIQ Oncology Information System

Reason

Order Status Remains Approved When Should Indicate Complete.

Action

On August 2018 the firm sent letter to all their customer with the following instructions; Recommended User Action: A user with appropriate pharmacy rights can unlock the record. This blanks out the details requiring the user to re-enter the administration details previously entered. To avoid this locking issue, close the MAR window before navigating to the CWS. This document contains important information for the continued safe and proper use of your equipment. Please post this notice in a place accessible to all users, e.g. Instructions for Use, until this action is closed. Advise the appropriate personnel working with this product the content of this letter. Elekta Corrective Actions: The issue is resolved in MOSAIQ Release 2.65 Beta 02 and in release 2.64 SP10. In order to meet regulatory requirements, you are required to complete this the Acknowledgement Form and return it to Elekta immediately upon receipt but no later than 30 days.

Distribution

AK, AZ, CA, CO, CT, DC, FL, GA, IA, ID, IL, KS, KY, LA, MA, MD, ME, MI, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, WA, WI, WV, and WY Australia, Canada, Ireland, New Zealand, Portugal, Singapore, South Africa, Spain, Sweden, and United Kingdom

Quantity

185