Elekta recalls Synergy, Harmony, Infinity, and Versa HD linear accelerators due to electrical grounding issues. Affected units may have safety risks during medical treatments.
Due to a manufacturing issue and electrical grounding of systems.
Elekta is recalling several types of medical linear accelerators because of electrical grounding problems. This could pose safety risks during radiation therapy treatments if the device malfunctions.
Electrical grounding issues could cause the device to malfunction during radiation therapy. This might lead to improper treatment delivery or safety hazards if the machine is not properly grounded.
Patients receiving radiation therapy at medical facilities using these specific Elekta linear accelerators are most at risk. Healthcare providers and facilities that use these devices may also be affected.
Check for the product names: Elekta Synergy, Harmony, Infinity, or Versa HD. Look for specific lot codes listed in the recall notice, such as 05060191071550 for Synergy.
Identify the lot code on your device's label to confirm if it matches the recalled units listed in the notice.
Reach out to your medical facility to determine if your device is affected and what steps they recommend.
The recall is due to a manufacturing issue with electrical grounding in these medical linear accelerators.
Yes, improper grounding could cause the device to malfunction during radiation therapy, potentially leading to unsafe treatment conditions.
Check the product name and lot code against the list provided in the recall notice: Synergy (lot 05060191071550), Harmony (lot 05060191071604), etc.
We’ve drafted a message you can send Elekta to request your refund or repair — edit it as you like.
Subject: Recall Z-1164-2026 — Elekta Elekta Hello, I own a Elekta that is covered by recall Z-1164-2026 from Elekta. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
