PTW FREIBURG recalls

Recall found. PTW FREIBURG is named in FDA Class II recall Z-3174-2026 covering Brand Name. Hazard: When a bolus is included in a treatment plan and sent for secondary dose calculation, the software accounts for it but does not display this clearly, which may lead users to incorrectly omit the bolus during treatment and deliver the prescribed dose to the wrong tissue depth. Identifying details: Model/Catalog Number: S070031.520; UDI-DI: +EPTWS070031Q5200; Software Version 3.1.18;. Status: Ongoing.

Models with recalls

Brand Name (1)

All PTW FREIBURG recalls

FDA Class II · Medical device · September 23, 2026

Brand Name recall — PTW FREIBURG

When a bolus is included in a treatment plan and sent for secondary dose calculation, the software accounts for it but does not display this clearly, which may lead users to incorr…

Official ID Z-3174-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.