FDA Device recall Z-0214-2026

GE Healthcare Carescape Central Station (CSCS) V3 MAS800 Desktop with software version V3.0.5, Part Number 5867474-03

FDA Device
Class II
ongoing
Published 2025-10-29

On 2025-10-29 the FDA classified a Class II recall of GE Healthcare Carescape Central Station (CSCS) V3 MAS800 Desktop with software version V3.0.5, Part Number 5867474-03 by Wipro Ge Healthcare Private, citing carescape Central Station (CSCS), software version V3.0.5, can cause the system to enter a continuous reboot cycle. If this occurs, a loss of central monitoring of connected patie….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0214-2026
Classification	Class II
Status	ongoing
Initiated	2025-09-05
Published	2025-10-29
Last updated	2026-09-13 11:57 UTC
Company	Wipro Ge Healthcare Private
Distribution	n/a

Product

GE Healthcare Carescape Central Station (CSCS) V3 MAS800 Desktop with software version V3.0.5, Part Number 5867474-03; Medical Display, cathode ray tube

Reason

Carescape Central Station (CSCS), software version V3.0.5, can cause the system to enter a continuous reboot cycle. If this occurs, a loss of central monitoring of connected patients could result. This issue occurs only when the number of central stations connected to the network is 118, 119 or 120.

Identifiers

code_info	GTIN 00195278343383, Serial Numbers: STV25225456SA, STV25225455SA, STV25266464SA, STV25235817SA, STV25235816SA, STV2528… GTIN 00195278343383, Serial Numbers: STV25225456SA, STV25225455SA, STV25266464SA, STV25235817SA, STV25235816SA, STV25286682SA, STV25225594SA, STV25235792SA, STV25235774SA, STV25225550SA, STV25235626SA, STV25235625SA, STV25184592SA, STV25235628SA, STV25235631SA, STV25184595SA, STV25235629SA, STV25235632SA, STV25235630SA, STV25276515SA, STV25225510SA, STV25276516SA, STV25225505SA, STV25225508SA, STV25225509SA, STV25225507SA, STV25225506SA, STV25113369SA, STV25204986SA, STV25205160SA, STV25205151SA, STV25205161SA, STV25062736SA, STV25256133SA, STV25225512SA, STV25296702SA, STV25296701SA, STV25296748SA, STV25256214SA, STV25225511SA, STV25256215SA, STV25256199SA, STV25256216SA, STV25256202SA, STV25225497SA, STV25225514SA, STV25225498SA, STV25256131SA, STV25256129SA, STV25256128SA, STV25296747SA, STV25256132SA, STV25256362SA, STV25225494SA, STV25225513SA, STV25296697SA, STV25256153SA, STV25296745SA, STV25256130SA, STV25256134SA, STV25256198SA, STV25296749SA, STV25296698SA, STV25256112SA, STV

code_info

GTIN 00195278343383, Serial Numbers: STV25225456SA, STV25225455SA, STV25266464SA, STV25235817SA, STV25235816SA, STV2528…

GTIN 00195278343383, Serial Numbers: STV25225456SA, STV25225455SA, STV25266464SA, STV25235817SA, STV25235816SA, STV25286682SA, STV25225594SA, STV25235792SA, STV25235774SA, STV25225550SA, STV25235626SA, STV25235625SA, STV25184592SA, STV25235628SA, STV25235631SA, STV25184595SA, STV25235629SA, STV25235632SA, STV25235630SA, STV25276515SA, STV25225510SA, STV25276516SA, STV25225505SA, STV25225508SA, STV25225509SA, STV25225507SA, STV25225506SA, STV25113369SA, STV25204986SA, STV25205160SA, STV25205151SA, STV25205161SA, STV25062736SA, STV25256133SA, STV25225512SA, STV25296702SA, STV25296701SA, STV25296748SA, STV25256214SA, STV25225511SA, STV25256215SA, STV25256199SA, STV25256216SA, STV25256202SA, STV25225497SA, STV25225514SA, STV25225498SA, STV25256131SA, STV25256129SA, STV25256128SA, STV25296747SA, STV25256132SA, STV25256362SA, STV25225494SA, STV25225513SA, STV25296697SA, STV25256153SA, STV25296745SA, STV25256130SA, STV25256134SA, STV25256198SA, STV25296749SA, STV25296698SA, STV25256112SA, STV

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0214-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.