Philips recalls GYROSCAN ACS-NT MRI systems with serial numbers starting with 5533, 5414, 5245, etc. due to potential incorrect installation of the patient support table floor plate, which could lead to patient safety issues during use.
Patient support table floor plate may be incorrectly installed.
Philips is recalling certain GYROSCAN ACS-NT MRI systems because the patient support table floor plate may be incorrectly installed. This could pose a risk of patient safety issues during medical procedures if the table is not properly secured.
The patient support table floor plate may be incorrectly installed, which could lead to the table shifting or becoming unstable during MRI procedures. This instability might cause patient injury or interfere with the MRI scan process.
Healthcare facilities using the recalled GYROSCAN ACS-NT MRI systems with specific serial numbers are most at risk. Patients undergoing MRI scans with these systems may be affected if the table is not correctly installed.
Check the serial number on the device's label. The recalled units have serial numbers starting with 5533, 5414, 5245, 5542, 5300, 5227, 5472, 5193, 5413, 5216, 5029, 5460, 5437, 5213, 5295, 5302, 5387, 5468, 5098, 5339, 5156, 5349, 5334, 5513, 5461, 5545, 5177, 5564, 5102, 5134, 5288, 5168, 5428, 5411, 5519, 5323, 5561, 5230, 5142, 5082, 5014, 5110, 5052, 5379, 5137, 5389, 5403, 5232, 5556, 5065.
Look for the serial number on the device label to confirm if it is in the list of recalled numbers.
The patient support table floor plate may be incorrectly installed, which could lead to instability during MRI procedures and potential patient safety issues.
Check the serial number to see if it is in the list of recalled numbers. If it is, contact Philips for further instructions.
The recall record does not specify a remedy, so no fix is mentioned.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1559-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1559-2024 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.
