Philips recalls Omnidiagnost Classic X-ray systems with specific product codes due to risk of uncontrolled table tilt from missing locking plate. Affected units may tilt unexpectedly and require immediate attention.
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 Omnidiagnost Classic X-ray systems with product codes 70859, 708023, 708024, and 708025 because the locking plate may be missing, causing the system to tilt unexpectedly and uncontrollably. This poses a risk of injury if the system tips during use.
The locking plate may be missing from the system, which can cause the X-ray table to tilt unexpectedly and uncontrollably. This tilt cannot be stopped by the user, potentially leading to falls or injuries during medical procedures.
Medical facilities using the Omnidiagnost Classic X-ray system are most at risk. Patients and staff could be injured if the system tilts unexpectedly during procedures.
Check for product codes 70859, 708023, 708024, or 708025 on the device. The recall applies to Omnidiagnost Classic X-ray systems sold in the U.S. by Philips North America.
Inspect the system to see if the locking plate is present and secure. If missing, stop using the system immediately.
Product codes 70859, 708023, 708024, and 708025 are affected.
The locking plate may be missing from the system, which can cause the X-ray table to tilt unexpectedly and uncontrollably.
Check if the locking plate is present. If missing, stop using the system immediately and contact Philips for further instructions.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1054-2019 — Philips Philips Hello, I own a Philips that is covered by recall Z-1054-2019 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.
