iGUIDE recallZ-2230-2019 · Elekta, Inc. · initiated Jun 19, 2019
Terminated
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Elekta, Inc. or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Potential for iGUIDE to incorrectly monitor the 3D position.
FDA root cause category: Software Design Change
What the company is doing
Elekta, Inc. notified customers on about 06/19/2019 via URGENT IMPORTANT FIELD SAFETY NOTIFICATION" letter. Customers were instructed to follow the below steps: 1. Log on to iGUIDE and move the 3D position. If the 3D position is equal to the PARK position, the system is not affected. 2. If the 3D position is not equal to the PARK position, log on to iGUIDE with Operator and Administrator rights. (If no user is available, go to the iGUIDE User Manager and add an appropriate user.). 3. Move the HexaPOD to the 3D Position (If 3D position is equal to the DRIVE position, both checkmarks will appear). 4. Open the HexaPOD properties (Left click the HexaPOD symbol on the system overview), which will display the HexaPOD properties. 5. Enter a rotation of 1.00 degree for any of the axis (RX, RY, RZ) and click Go to position. 6. Execute the pending movement. If the checkmark for the 3D position disappears and the EXTERNAL INHIBIT is set, your system is not affected by the comma / dot issue. No further actions are necessary. If the 3D position monitoring does not consider the 1.00 degree and the checkmark for the 3D position is still displayed and the EXTERNAL INHIBIT is not set, your system is affected! If the customer wants to still use a 3D workflow without imaging, do not rely on the 3D position indicator in iGUIDE. The HexaPOD should be moved to the PARK position first, then the 3D workflow can be started moving the HexaPOD back to the 3d position. Customers were also instructed to place the recall notice in a place accessible to all users (e.g. Instructions for Use, until this action is closed) and to advise the appropriate personnel, working with this product, on the content of this letter. A technical solution (iGUIDE patch) will be provided to correct the behavior. Until the iGUIDE patch is available, an interim solution can be implemented (change comma to dot) if your system is affected. Please consult your local Elekta represent
Recall details
- Recall number
- Z-2230-2019
- Status
- Terminated
- Initiated by the company
- Jun 19, 2019
- Recalling firm
- Elekta, Inc.
- Quantity
- 374 devices
- Product code
- IYE
- FDA submissions
- K072079
- Distribution
- Nationwide distribution to AK, AL, CA, CO, CT, FL, GA, ID, IL, IN, KY, LA, MA, MD, MI, MN, MO, MT, NC, ND, NM, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, VA, VT, WA, WI. Worldwide distribution to Algeria, Argentina, Australia, Austria, Belgium, Botswana, Canada, Chile, China, Colombia, Cyprus, Czech Republic, Denmark, Egypt, France, Germany, Hong Kong, India, Indonesia, Ireland, Israel, Italy, Japan, Jordan, Korea, Republic of, Malaysia, Mexico, Morocco, Netherlands, New Zealand, Norway, Poland, Portugal, Romania, Slovakia, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, United Kingdom, Vietnam.
Product description
iGUIDE System with software build iGuide 2.2.0, 2.2.1, and 2.2.2
Code information (models, lots, serial numbers)
Version 2.2.0, Product Code/GTIN Number: 04056719001704; Version 2.2.1, Product Code/GTIN Number: 04056719001742; Version 2.2.2, Product Code/GTIN Number: 04056719002039
Devices named in this recall
3 devices in the FDA device registry whose identifier appears in the recall's code information.
- iGUIDE P10603-1103C-Medical Intelligence GmbH · Accelerator, Linear, Medical2 recalls1 report
- iGUIDE P10603-1093C-Medical Intelligence GmbH · Accelerator, Linear, Medical2 recalls0 reports
- iGUIDE P10603-1113C-Medical Intelligence GmbH · Accelerator, Linear, Medical2 recalls0 reports
Product lines
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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