Philips recalls Azurion 7 surgical imaging systems with Certeray generator due to risk of power loss from short circuits in the power inverter board, which could delay or terminate procedures.
Generator may fail due to a potential short circuit in the Printed Circuit Board Assembly (PCBA) in PoInt EVR (Power Invertor). If a short circuit occurs, it will cause the fuses to trip and the system will become non-functional due to power loss, resulting in a potential delay of procedure or termination of procedure.
Philips is recalling Azurion 7 surgical imaging systems with Certeray generators because a short circuit in the power inverter board could cause power loss, potentially delaying or ending procedures. This affects specific models sold in the US.
A short circuit in the printed circuit board assembly (PCBA) of the power inverter could cause fuses to trip, leading to power loss. This might interrupt surgery procedures, causing delays or termination of the procedure.
Surgical teams using the Azurion 7 with Certeray generator for imaging procedures in hospitals or clinics. Patients undergoing surgery with this equipment are at risk of procedure delays or termination.
Check for model numbers 722223, 722224, 722225, or 722226. US units have specific serial numbers and UDI codes listed in the recall notice.
Identify the model number on your device (722223, 722224, 722225, or 722226) to confirm if it's affected.
Reach out to Philips customer support for further assistance with the recall.
Philips is recalling these devices because a short circuit in the power inverter board could cause power loss, potentially delaying or terminating surgical procedures.
Models 722223, 722224, 722225, and 722226 sold in the US.
No, but you should check your model number and contact Philips if you have an affected device.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1178-2024 — Philips Philips Hello, I own a Philips that is covered by recall Z-1178-2024 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.
