Philips recalls Zenition 70 ultrasound systems with wireless foot switch model 718133 due to potential procedure interruptions from firmware issues. Affected units may require repair or replacement.
Firm discovered that the wireless foot switch can suddenly stop responding due to a firmware issue. If the wireless foot switch fails, there could be a delay or interruption of procedure if the hand switch is not used or if the wired foot switch is not connected to the system.
Philips is recalling Zenition : 70 ultrasound systems with model number 718133 because a firmware issue could cause the wireless foot switch to stop working, potentially interrupting medical procedures. This is serious for healthcare providers using the device during surgeries or imaging.
The wireless foot switch may suddenly stop responding due to a firmware issue. If the switch fails, it could delay or interrupt medical procedures if the hand switch isn't used or the wired foot switch isn't connected to the system.
Healthcare providers using Philips Zenition 70 ultrasound systems with model number 718133 are most at risk. Patients undergoing procedures with these systems could be affected if the wireless foot switch fails.
Check for model number 718133 on the Zenition 70 ultrasound system. The wireless foot switch model numbers are 459801238191 or 459801238231.
Verify your Zenition 70 system has model number 718133 and wireless foot switch model numbers 459801238191 or 459801238231.
Philips discovered a firmware issue that can cause the wireless foot switch to stop responding, potentially interrupting medical procedures.
The recall record does not specify a remedy, so contact Philips directly for guidance.
The hazard could cause procedure interruptions if the wireless foot switch fails, but the recall does not mention serious injury risks.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0648-2022 — Philips Philips Hello, I own a Philips that is covered by recall Z-0648-2022 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.
