# FDA recall Z-2523-2026

> **Philips North America Llc** · Class II · device recall initiated 2026-05-26.

## Product

Philips Avalon Fetal Monitor, FM 30 Part numberM2703A

## Reason for recall

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.

## 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.

## Key facts

- **Recall number:** Z-2523-2026
- **Recalling firm:** Philips North America Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-26
- **Report date:** 2026-07-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Cambridge, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2523-2026

## Citation

> MORVS. FDA recall Z-2523-2026. Retrieved 2026-10-23 from https://api.morvs.ai/recall/Z-2523-2026. Source: US FDA. Licensed CC0.

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