Elekta, Inc. Desktop Pro R6.0 & R6.1, Linear Medical Accelerator. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Desktop Pro R6.0 & R6.1, Linear Medical Accelerator.
Brand
Elekta, Inc.
Lot Codes / Batch Numbers
with the exception of Sigma Micro Users)
Products Sold
Model number MRT 9871/ MRT 10601 (This issue affects Desktop Pro 6.0 and 6.1 users with a 3rd party R & V System, with the exception of Sigma Micro Users)
Elekta, Inc. is recalling Desktop Pro R6.0 & R6.1, Linear Medical Accelerator. due to Unexpected Diaphragm movement when manual field size modifications are not saved.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Unexpected Diaphragm movement when manual field size modifications are not saved.
Recommended Action
Per FDA guidance
Consignees were notified by letter on/about 11/23/2006
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AZ, CA, CO, FL, GA, IA, MI, NV, OH, OK, PA, WA, WV
Page updated: Jan 10, 2026