Philips recalls specific models of Ingenuity Core X-Ray tubes with a production defect causing oil leakage. This could pose a risk for patients or users if the tube housing leaks oil. Affected units have unique serial numbers and UDI codes.
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 is recalling certain Ingenuity Core X-Ray tubes due to a production defect that may cause oil leakage from the tube housing. This could pose a risk to patients or users if the leakage occurs. The affected units have specific serial numbers and UDI codes.
The X-Ray tube has a production defect that allows oil to leak from the housing. If this leakage reoccurs, it could pose a risk to patients or users. The defect is specific to the affected models.
Medical facilities using the recalled Philips Ingenuity Core X-Ray tubes are most at risk. Patients and medical staff who use these tubes could be affected if the oil leakage occurs.
Check for the serial numbers: 310375, 310377, 333169, 333171, or 333172. The UDI codes are (01)00884838059498(21) followed by these serial numbers.
Verify if your X-Ray tube has a serial number of 310375, 310377, 333169, 333171, or 333172.
The X-Ray tube has a production defect that allows oil leakage from the tube housing if it reoccurs.
Check for the serial numbers: 310375, 310377, 333169, 333171, or 333172. The UDI codes are (01)00884838059498(21) followed by these serial numbers.
The recall does not specify a remedy, so contact Philips directly 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-2274-2018 — Philips Philips Hello, I own a Philips that is covered by recall Z-2274-2018 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.
