Philips recalls wireless foot switches for Allura Xper and Azurion X-ray systems due to potential loss of availability during procedures. Affected models include 722001-722079.
Loss of availability of the wireless foot switch during procedures.
Philips is recalling wireless foot switches used with Allura Xper and Azurion X-ray systems because they may become unavailable during medical procedures. This could disrupt surgery or imaging work if the switch fails to function properly.
The wireless foot switch may become unavailable during procedures, meaning it could stop working when needed. This might cause delays or interruptions in medical imaging or surgery. However, the risk is not severe as it does not involve physical harm or injury.
Medical professionals using Philips Allura Xper or Azurion X-ray systems with the recalled wireless foot switches are affected. The risk is low as the issue is limited to system availability during procedures, not immediate safety hazards.
Check if your Philips Allura Xper or Azurion X-ray system has a wireless foot switch with model numbers 722001 through 722079. The lot numbers listed in the recall notice also indicate specific batches.
Identify the model number of your wireless foot switch to see if it matches the recalled list (722001-722079).
Reach out to Philips customer support for guidance on whether your specific model is affected and what to do next.
The wireless foot switch may become unavailable during procedures, which could disrupt medical imaging or surgery. This is not a safety hazard but a functional issue.
No, the recall does not require immediate discontinuation. The issue is limited to potential unavailability during procedures, not a safety risk.
Check the model number on your wireless foot switch; affected models are listed as 722001 through 722079 in the recall notice.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2485-2023 — Philips Philips Hello, I own a Philips that is covered by recall Z-2485-2023 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.
