Elekta recalls Unity devices with specific serial numbers due to rare risk of speakers becoming dislodged and pulled into the bore during use, potentially causing injury.
In rare circumstances, due to reasons such as inadequate hospital facility maintenance, water leakage, and weakening of speaker fixings during the lifetime of the system, the speakers can become dislodged and be pulled into the bore.
Elekta is recalling specific Unity devices because in rare cases, speakers can become dislodged and pulled into the bore, which could cause injury. This issue is linked to hospital facility maintenance, water leakage, and weakening of speaker fixings over time.
The speakers can become dislodged due to water leakage, poor hospital facility maintenance, or weakening of the speaker fixings over time. When dislodged, they can be pulled into the bore, potentially causing injury.
Hospital staff and patients using the Elekta Unity devices are most at risk, particularly in settings with inadequate maintenance or water exposure.
Check for the Elekta Unity device with serial numbers 1536549. This recall applies to specific units sold in hospitals.
Verify the device has serial numbers 1536549 to confirm it is affected.
The recall is due to rare cases where speakers can become dislodged and pulled into the bore, caused by water leakage, poor hospital facility maintenance, or weakening of speaker fixings over time.
Check for the Elekta Unity device with serial numbers 1536549. This recall applies to specific units sold in hospitals.
The recall does not specify a remedy, so contact Elekta Limited directly for guidance on next steps.
We’ve drafted a message you can send Elek:ta to request your refund or repair — edit it as you like.
Subject: Recall Z-0706-2019 — Elek:ta Elek:ta Hello, I own a Elek:ta that is covered by recall Z-0706-2019 from Elek:ta. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
