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Terminated

Elekta Unity, Image-Guided Radiation Therapy System

FDA Recall Z-2473-2020 · Posted None

Recalling FirmElekta, Inc.
Recall StatusTerminated
Product CodeIYE
Date Initiated2019-12-18
Date Terminated2021-06-15
Product Quantity21 devices

Reason for Recall

There have been reports of excessive heating in the MRL Gradient Connection Module.

Firm Action

Initially, the firm issued an email on 12/18/2019 to their field engineers which said they had attached a "Knowledge Article" which provided instructions on how to inspect the Philips Marlin 1.5T system used in the Elekta Unity MR Linac. On 5/11/2020, the firm issued an Urgent Important Field Safety Notification dated May, 2020, via email to consignees which explained the problem, clinical impact, and said that initial corrective actions have been performed on all impacted sites to ensure the gradient coil connection assembly is correct. It goes onto say that extensive testing of the incorrect connection material has been completed to ensure that continued use of the Elekta Unity system is acceptable, however, it remained that further actions can be taken to reduce the risk.

Root Cause

Process control

Distribution Pattern

Distributed in US - PA, NY, and IA. Distributed ROW - Australia, Canada, China, Switzerland, Denmark, Hong Kong, Italy, Netherlands, Sweden, Thailand, Turkey, UK. There was no government/military distribution.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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