FDASeptember 17, 2021device

Elekta Medical Linear Accelerator (EMLA), configured as follows: a. Elekta Precise Digital Accelerator; b. Elekta Harmony; c. Elekta Synergy; d. Elekta Infinity; e. Versa HD

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There is a risk that the Diode D1 in the Modulator can fail in a destructive manner when removed from the machine, and that the protective tube surrounding the diode may fail to contain the ejected matter.

What to do

FDA enforcement status: Terminated

Brands named

elekta

UPCs

5060191071017050601910715810506019107155005060191071543050601910715120506019107157405060191071529

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Elekta Medical Linear Accelerator (EMLA), configured as follows: a. Elekta Precise Digital Accelerator; b. Elekta Harmony; c. Elekta Synergy; d. Elekta Infinity; e. Versa HD — Recall Details · AllClear