Philips Medical recalls specific Ingenuity Core128 X-Ray Tube models with a production defect causing oil leakage. Affected units may pose patient or user risks if oil leaks occur.
A problem has been detected in the X-Ray Tube. The affected tubes have a production defect that allows oil leakage from the tube housing, if it were to re-occur, could pose a risk for patients or users.
Philips Medical is recalling certain Ingenuity Core128 X-Ray Tubes due to a production defect that could cause oil leakage. This leakage poses a risk to patients or users if it occurs, requiring immediate attention to prevent potential harm.
The X-Ray Tube has a production defect that allows oil to leak from the tube housing. If this leakage reoccurs, it could pose a risk to patients or users during medical procedures.
Healthcare professionals using the Ingenuity Core128 X-Ray Tube models with serial numbers 320403-336323 are most at risk. Patients receiving scans with these units may also be affected.
Check for the serial numbers 320403, 320405, 320406, 336321, 320411, 336323, or 320425 on the X-Ray Tube. The affected units were sold with the UDI (Unique Device Identifier) codes listed in the recall notice.
Look for the serial numbers 320403, 320405, 320406, 336321, 320411, 336323, or 320425 on the X-Ray Tube.
The X-Ray Tube has a production defect that allows oil to leak from the tube housing if it reoccurs.
Check for the serial numbers 320403, 320405, 320406, 336321, 320411, 336323, or 320425 on the X-Ray Tube.
The recall does not specify a remedy, so contact Philips Medical directly for guidance.
We’ve drafted a message you can send Philips Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2275-2018 — Philips Medical Philips Medical Hello, I own a Philips Medical that is covered by recall Z-2275-2018 from Philips Medical. 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.
