Deerfield Imaging recalls IMRIS T2X operating tables with specific part numbers due to potential unintended movement during use. Affected units may drift while in operation, requiring immediate action.
The Operating Room Table may drift while in use, which could potentially result in unintended movement of the table.
Deerfield Imaging has recalled specific models of IMRIS T2X operating tables because they may drift while in use, potentially causing unintended movement. This could lead to safety risks during medical procedures if the table shifts unexpectedly.
The operating table may drift while in use, which could cause unintended movement. This poses a risk of the table shifting during medical procedures, potentially leading to injuries or disruptions in patient care.
Medical facilities using the recalled IMRIS T2X tables are most at risk. Patients and staff could be affected if the table moves unexpectedly during surgery or procedures.
Check for part numbers: 108000-000, 108000-600, 109682-000, or 109682-600. Serial numbers for each part number are listed in the recall notice.
Identify if your table has part numbers 108000-000, 108000-600, 109682-000, or 109682-600.
Reach out to Deerfield Imaging for further instructions on safe use or potential remedies.
The IMRIS T2X table may drift while in use, which could result in unintended movement during medical procedures.
Part numbers 108000-000, 108000-600, 109682-000, and 109682-600 are affected.
Check the part numbers listed in the recall notice: 108000-000, 108000-600, 109682-000, or 109682-600. Each has specific serial numbers.
We’ve drafted a message you can send Deerfield Imaging to request your refund or repair — edit it as you like.
Subject: Recall Z-1265-2018 — Deerfield Imaging Deerfield Imaging Hello, I own a Deerfield Imaging that is covered by recall Z-1265-2018 from Deerfield Imaging. 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.
