Philips recalls Achieva 1.5T MRI systems with model numbers 781196, 781296, 781343. Patient support table floor plates may be incorrectly installed, potentially causing safety issues during use.
Patient support table floor plate may be incorrectly installed.
Philips is recalling certain Achieva 1.5T MRI systems because the patient support table floor plate may be incorrectly installed. This could lead to safety risks during medical procedures. Affected units have specific model and serial numbers listed in the recall notice.
The patient support table floor plate may be incorrectly installed, which could lead to safety issues during medical procedures. However, the recall does not specify a mechanism that would cause injury or serious harm under normal use conditions.
Medical facilities that own or use Philips Achieva 1.5T MRI systems with model numbers 781196, 781296, or 781343 are most at risk. The recall applies to specific serial numbers listed in the official notice.
Check if your Philips Achieva 1.5T MRI system has model numbers 781196, 781296, or 781343. Affected units also have specific serial numbers listed in the recall notice.
Verify your model number and serial number against the list provided in the recall notice to determine if your unit is affected.
The patient support table floor plate may be incorrectly installed, which could lead to safety issues during medical procedures.
Check if your Philips Achieva 1.5T MRI system has model numbers 781196, 781296, or 781343. Affected units also have specific serial numbers listed in the recall notice.
The recall notice does not specify a remedy; affected units should check their model and serial numbers to determine if they are affected.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1550-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1550-2024 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.
