Deerfield Imaging recalls IMRIS ORT 200 operating room tables with specific part numbers due to risk of drifting in roll position during use. Affected units include models 113821-000, 113821-600, 114148-000, and 114148-600.
Table may drift in the roll position while in use
Deerfield Imaging has recalled IMRIS ORT 200 operating room tables that may drift in roll position while in use. This could cause instability during medical procedures, potentially leading to patient injury if the table moves unexpectedly.
The table may shift or drift in the roll position while being used, which could cause instability. This instability might lead to patient injury if the table moves unexpectedly during medical procedures.
Healthcare facilities using the IMRIS ORT 200 operating room table with specific part numbers are most at risk. Patients undergoing procedures on these tables could be affected if the table drifts.
Check for part numbers: 113821-000, 113821-600, 114148-000, or 114148-600. Serial numbers are listed for each part number in the recall notice.
Identify the part number on your IMRIS ORT 200 table to see if it matches the recalled models.
Reach out to Deerfield Imaging for further instructions on how to address the issue.
Part numbers 113821-000, 113821-600, 114148-000, and 114148-600 are affected.
Check the part number on your table against the listed affected part numbers: 113821-000, 113821-600, 114148-000, or 114148-600.
Contact Deerfield Imaging for instructions on how to address the issue, as the recall does not specify a remedy.
We’ve drafted a message you can send Deerfield Imaging to request your refund or repair — edit it as you like.
Subject: Recall Z-0647-2019 — Deerfield Imaging Deerfield Imaging Hello, I own a Deerfield Imaging that is covered by recall Z-0647-2019 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.
