# FDA device recall: Philips Avalon Fetal Monitor, FM 30 Part numberM2703A

> recall · VERIFIED · 2026-05-26

Firm: Philips North America Llc · Class II · 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.

- Company: Philips North America Llc
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.