Philips recalls URODiagnost Eleva X-ray systems with product codes 708026-708028 due to potential missing locking plate causing uncontrolled table tilt during use. Affected units may require inspection or replacement.
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 URODiagnost Eleva X-ray systems with product codes 708026, 708027, and 708028. The locking plate may be missing, which could cause the table to tilt unexpectedly and cannot be stopped by the user.
The locking plate may be missing from the system, which can cause the table to tilt unexpectedly during use. This tilt cannot be stopped by the user, potentially leading to equipment damage or injury if the table moves while a patient is being examined.
Users of the Philips URODiagnost Eleva X-ray system with product codes 708026, 708027, or 708028 are affected. Medical professionals who use this equipment for procedures like urography or angiography are most at risk.
Check for product codes 708026, 708027, or 708028 on the URODiagnost Eleva X-ray system. These units were sold in the U.S. between 2019 and 2023.
Inspect the system for a missing locking plate that could cause uncontrolled table tilt.
Product codes 708026, 708027, and 708028.
The locking plate prevents unexpected table tilt during use. If missing, the table may tilt uncontrollably, potentially causing injury or equipment damage.
No, but you should check for a missing locking plate before use. If the plate is missing, contact Philips for guidance.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1056-2019 — Philips Philips Hello, I own a Philips that is covered by recall Z-1056-2019 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.
