medical MODERATE Updated 2026-06-17

Elekta, Inc. recalls MOSAIQ Oncology Information System

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Recalled Product

MOSAIQ Oncology Information System

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Hazard / Issue

Software may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Software Version: MOSAIQ 3.2/UDI: 07340201500071

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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Search Amazon for MOSAIQ Oncology Information System →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

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