Reported Jul 1, 2026 · Ongoing

Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A

Philips North America LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Philips North America Llc · 222 Jacobs St · Cambridge, MA · 02141-2289

Is this the product you have?

    • Philips Avalon Fetal Monitor
    • FM20
    • Part number M2702A
    • Part M2703A
Lot codes and dates
  • UDI/DI 00884838000407
  • Serial Numbers

    66 of 66 codes

    • DE79569306
    • DE79569332
    • DE79569360
    • DE79569417
    • DE79569442
    • DE79569482
    • DE79569307
    • DE79569470
    • DE79569390
    • DE79569356
    • DE79569452
    • DE79569289
    • DE79569302
    • DE79569536
    • DE79569358
    • DE79569343
    • DE79569457
    • DE79569353
    • DE79569373
    • DE79569411
    • DE79569491
    • DE79569615
    • DE79569287
    • DE79569338
    • DE79569437
    • DE79569459
    • DE79569473
    • DE79569340
    • DE79569308
    • DE79569377
    • DE79569286
    • DE79569304
    • DE79569327
    • DE79569330
    • DE79569347
    • DE79569352
    • DE79569400
    • DE79569418
    • DE79569431
    • DE79569436
    • DE79569456
    • DE79569469
    • DE79569474
    • DE79569588
    • DE79569326
    • DE79569424
    • DE79569487
    • DE79569547
    • DE79569290
    • DE79569258
    • DE79569367
    • DE79569370
    • DE79569380
    • DE79569388
    • DE79569311
    • DE79569440
    • DE79569460
    • DE79569527
    • DE79569462
    • DE79569299
Amount recalled
285 units

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 3:26 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.