Philips recalls MultiDiagnost Eleva w/ Flat Detector (model codes 708034, 708037, 708038) due to possible missing locking plate causing uncontrolled table tilt during medical procedures.
The locking plate may be missing from the system, which may result in unexpected stand/table tilt movement that cannot be stopped by the user.
Philips is recalling certain MultiDiagnost Eleva w/ Flat Detector models because the locking plate might be missing, which could cause the table to tilt unexpectedly during medical procedures. This poses a risk of injury to patients or staff if the tilt isn't stopped.
The locking plate may be missing from the system, which can cause the table to tilt unexpectedly and cannot be stopped by the user. This could lead to patient or staff injury during medical procedures if the tilt occurs while the system is in use.
Medical facilities using the recalled models (708034, 708037, 708038) are most at risk, particularly during procedures involving patient imaging where the table might tilt unexpectedly.
Check for product codes 708034, 708037, or 708038 on the MultiDiagnost Eleva w/ Flat Detector. These models were sold in the U.S. for medical imaging procedures.
Inspect the system for a missing locking plate that could cause uncontrolled table tilt during use.
The locking plate may be missing from the system, which can cause unexpected table tilt that cannot be stopped by the user during medical procedures.
Product codes 708034, 708037, and 708038 for the MultiDiagnost Eleva w/ Flat Detector.
No, but you should check for a missing locking plate before use. If you find the plate missing, take steps to prevent uncontrolled tilt.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1055-2019 — Philips Philips Hello, I own a Philips that is covered by recall Z-1055-2019 from Philips. 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.
