Philips recalls Avalon Fetal Monitors (FM20) with part numbers M2702A and M2703A due to incorrect speaker connector assembly that may cause intermittent or permanent loss of speaker output.
Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.
Philips is recalling Avalon Fetal Monitors (FM20) with specific part numbers because the speaker connector assembly is incorrect. This could lead to the device cables being pulled out of the housing, causing the monitor to lose sound intermittently or permanently.
The monitor's speaker connector is assembled incorrectly, which can cause the device cables to be pulled out of the housing. This may result in intermittent or permanent loss of speaker output, meaning the monitor might not produce sound during use.
Pregnant individuals using the Philips Avalon Fetal Monitor (FM20) with part numbers M2702A or M2703A are affected. Healthcare providers and expectant parents who use this monitor are most at risk.
Check for part numbers M2702A or M2703A on the Philips Avalon Fetal Monitor (FM20). The serial numbers listed in the recall include DE79569306 through DE79569588.
Look for part numbers M2702A or M2703A on the Philips Avalon Fetal Monitor (FM20).
The monitor has an incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.
Part numbers M2702A and M2703A for the Philips Avalon Fetal Monitor (FM20).
Check the part numbers on your monitor; affected units have part numbers M2702A or M2703A with serial numbers listed in the recall.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-2522-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-2522-2026 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.
