Philips recalls MultiDiagnost-Eleva imaging systems with product codes 708032 and 708036 due to potential 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 two specific models of its MultiDiagnost-Eleva imaging systems (product codes 708032 and 708036) because the locking plate might be missing, which could cause the table to tilt unexpectedly and uncontrollably during medical procedures.
The locking plate may be missing from the system, which can cause the imaging table to tilt unexpectedly and uncontrollably during medical procedures. This could lead to patient injury if the table moves suddenly while the patient is being treated.
Healthcare providers using the MultiDiagnost-Eleva imaging systems for medical procedures are most at risk. Patients undergoing imaging treatments with these systems could be affected if the table tilts unexpectedly.
Check for product codes 708032 or 708036 on the imaging system. These models are used for multifunctional imaging applications including fluoroscopy, radiography, and angiography in medical settings.
Inspect the system for a missing locking plate that could cause uncontrolled table tilt during procedures.
The locking plate may be missing from the system, which could cause the imaging table to tilt unexpectedly and uncontrollably during medical procedures.
Product codes 708032 and 708036 for the MultiDiagnost-Eleva imaging system.
The recall record does not specify a remedy or fix.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1052-2019 — Philips Philips Hello, I own a Philips that is covered by recall Z-1052-2019 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.
