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FDA
Food and Drug Administration · Recall Z-2522-2026 · May 26, 2026

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

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, FM20, Part number M2702A, Part M2703A

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 00884838000407Model Serial Numbers: DE79569306Model DE79569332Model DE79569360Model DE79569417Model DE79569442Model DE79569482Model DE79569307Model DE79569470Model DE79569390Model DE79569356Model DE79569452Model DE79569289Model DE79569302Model DE79569536Model DE79569358Model DE79569343Model DE79569457Model DE79569353Model DE79569373Model DE79569411Model DE79569491Model DE79569615Model DE79569287Model DE79569338UPC 00884838000407

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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.