Elekta recalls Integrity R1.2 devices with potential positional errors after automatic table movement. Affected units have product code 90I--YE. No serial number.
Potential for positional errors following automatic table movement (ATM).
Elekta is recalling its Integrity R1.2 surgical table models that may cause positional errors when the automatic table moves. This could lead to incorrect positioning of patients during surgery, potentially causing injury.
The automatic table movement feature may cause the table to shift position incorrectly during surgical procedures. This could result in improper patient positioning, potentially causing injury during surgery.
Surgical staff and patients using Elekta Integrity R1.2 tables with product code 90I--YE. Those operating the tables during procedures are most at risk.
Check for the product code 90I--YE on the table. These models do not have serial numbers.
Look for the product code 90I--YE on the table. These models do not have serial numbers.
The product code is 90I--YE.
No, these models do not have serial numbers.
Check for the product code 90I--YE on the table. These models do not have serial numbers.
We’ve drafted a message you can send Elekta to request your refund or repair — edit it as you like.
Subject: Recall Z-0724-2018 — Elekta Elekta Hello, I own a Elekta that is covered by recall Z-0724-2018 from Elekta. 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.
