Philips recalls Veradius Unity model 718132 due to wireless foot switch firmware issues that may cause procedure delays if hand or wired switches aren't used. Affected units have specific serial numbers.
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 Veradius Unity medical devices with model number 71813:22 due to a wireless foot switch firmware issue that could cause procedure delays if the hand switch isn't used or the wired switch isn't connected. This is a safety concern for medical procedures where timing is critical.
The wireless foot switch may suddenly stop working due to a firmware problem. If this happens and the hand switch isn't used or the wired switch isn't connected, it could cause delays or interruptions in medical procedures.
Medical professionals using Veradius Unity systems with the specific model number 718132 are most at risk, as the issue could disrupt critical procedures during surgery or other medical treatments.
Check for the model number 718132 on the Veradius Unity device. Affected units have wireless foot switch serial numbers 459801238191 or 459801238231.
Ensure the wireless foot switch is connected to the system and the hand switch is functional if the wired switch is not in use.
No, only Veradius Unity model 718132 with specific wireless foot switch serial numbers 459801238191 or 459801238231 are affected.
If the wireless foot switch stops working, check if the hand switch is used or the wired switch is connected to the system to avoid procedure delays.
The recall record does not mention a specific fix or remedy; the remedy field is null.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-0649-2022 — Philips Philips Hello, I own a Philips that is covered by recall Z-0649-2022 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.
