medical MODERATE Updated 2026-07-08

RAYSEARCH LABORATORIES AB recalls RayCare 2024A SP1. Oncology Information Systems.

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Recalled Product

RayCare 2024A SP1. Oncology Information Systems.

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Hazard / Issue

Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during a treatment session, the user is not notified of the change.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Software Version 8.0.1.60193, UDI 0735000201083920240906, Expiration Date: 2030-01-24

✅ 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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