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FDA
Food and Drug Administration · Recall Z-2523-2026 · May 26, 2026

Philips Avalon Fetal Monitor, FM 30 Part numberM2703A

Philips North America Llc

The hazard

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. FDA Class II recall.

The remedy

Follow FDA guidance

About this recall

Philips Avalon Fetal Monitor, FM 30 Part numberM2703A

Affected identifiers

Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.

Model UDI/DI 00884838000414Model Serial Numbers: DE79646555Model DE79646616Model DE79646645Model DE79646647Model DE79646651Model DE79646697Model DE79646702Model DE79646746Model DE79646754Model DE79646757Model DE79646758Model DE79646762Model DE79646765Model DE79646775Model DE79646776Model DE79646783Model DE79646857Model DE79646891Model DE79646924Model DE79646750Model DE79646751Model DE79646756Model DE79646804Model DE79646592UPC 00884838000414

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Sourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.