Philips Avalon Fetal Monitor — Class II medical device recall Z-2523-2026
Ongoing recall by Philips North America Llc, reported 2026-07-01, distributed nationwide. Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the
| Recall number | Z-2523-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips North America Llc, Cambridge, MA, United States |
| Recall initiated | 2026-05-26 |
| Classified | 2026-06-22 |
| Reported by FDA | 2026-07-01 |
| Distributed | Nationwide (US) |
| Quantity | 169 units |
| UPC / GTIN / UDI-DI | 00884838000414 |
| Serial numbers | DE79646555, DE79646592, DE79646604, DE79646606, DE79646616, DE79646640, DE79646644, DE79646645, DE79646647, DE79646648, DE79646651, DE79646653, DE79646654, DE79646660, DE79646675, DE79646676, DE79646683, DE79646694, DE79646697, DE79646699, DE79646701, DE79646702, DE79646706, DE79646709, DE79646723 and 48 more |
| Model numbers | M2703A |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2523-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.