Data Foundry

Medical device recalls 2025

Portrait VSM Model nos — Class II medical device recall Z-0456-2026

Ongoing recall by GE Healthcare Finland Oy, reported 2025-11-19, distributed nationwide. Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lo

Recall numberZ-0456-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmGE Healthcare Finland Oy, Helsinki, Finland
Recall initiated2025-09-26
Classified2025-11-07
Reported by FDA2025-11-19
DistributedNationwide (US)
Quantity5,990
UPC / GTIN / UDI-DI00195278561312
Serial numbersSWP24140086WA, SWP24140087WA, SWP25040956SA, SWP25040958SA, SWP25040959SA, SWP25040960SA, SWP25040961SA, SWP25040962SA, SWP25040963SA, SWP25040964SA, SWP25040965SA, SWP25040966SA, SWP25040967SA, SWP25040968SA, SWP25040969SA, SWP25040970SA, SWP25040971SA, SWP25040972SA, SWP25040973SA, SWP25040974SA, SWP25040975SA, SWP25040976SA, SWP25040977SA, SWP25040978SA, SWP25040979SA and 475 more
Model numbers6660000-666

Product

Portrait VSM Model nos. 6660000-666 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms

Reason for recall

Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.

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-0456-2026. 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.