Philips North America Llc: Philips Avalon Fetal Monitor, Fm20, Part Number M2702a, Part M2703a

Recall Summary Philips is recalling certain Avalon Fetal Monitor FM20 models due to incorrect assembly of the speaker connector that can cause cables to detach from the device housing. This defect may result in loss of speaker output, either temporarily or permanently. The affected monitors were distributed nationwide in the US and in numerous countries worldwide.

Recalling firm

Philips North America Llc

Product

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

Reason

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.

Classification

Class II

Category

medical device recall

Country

United States

Agency

U.S. Food and Drug Administration

Recall date

2026-05-26

Status

Ongoing

Areas affected

AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...

Distribution

Worldwide distribution - US Nationwide and The countries of AE, AT, AU, BE, BG, BH, BR, CA, CH, CN, CR, CZ, DE, ES, FI, FR, GB, GR, HK, ID, IL, IN, IT, JO, JP, KR, KR, LT, LU, LV, MX, MY, NL, NZ, OM, SA, SE, SG, SI, TR, TW, ZA.

Official recall notice from U.S. Food and Drug Administration

Recall details on Nibble Recalls: https://trynibble.app/recalls/bcefcbf4-81f1-4ed0-8f91-b4dfec460485