FDA Device recall Z-0487-2018

GE HEALTHCARE CARESCAPE Central Station (CSCS) software version 2.0.2 The CARESCAPE Central Station is intended to collect information from…

FDA Device
Class II
terminated
Published 2018-02-07

On 2018-02-07 the FDA classified a Class II recall of GE HEALTHCARE CARESCAPE Central Station (CSCS) software version 2.0.2 The CARESCAPE Central Station is intended to collect information from… by Ge Medical Systems Information Technologies, citing CARESCAPE Central Station (CSCS) software version 2.0.2 units may experience unexpected NO COMM (No Communication) and network communication issues after boot-up or system restart.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0487-2018
Classification	Class II
Status	terminated
Initiated	2018-01-11
Published	2018-02-07
Last updated	2026-09-13 11:54 UTC
Company	Ge Medical Systems Information Technologies
Distribution	US

Product

GE HEALTHCARE CARESCAPE Central Station (CSCS) software version 2.0.2 The CARESCAPE Central Station is intended to collect information from a network and display this data. This data includes physiological, patient demographic and/or other non-medical information. Physiological parameters and waveforms from monitors and telemetry systems can be displayed, provide alarm annunciation, and can be printed from the CARESCAPE Central Station.

Reason

CARESCAPE Central Station (CSCS) software version 2.0.2 units may experience unexpected NO COMM (No Communication) and network communication issues after boot-up or system restart.

Identifiers

code_info	Model, Catalogue, or Code/ UDI/ Mfg. Lot or Serial Number Model, Catalogue or Code # UDI # Mfg. Lot or Serial # 20… Model, Catalogue, or Code/ UDI/ Mfg. Lot or Serial Number Model, Catalogue or Code # UDI # Mfg. Lot or Serial # 2092670-001-510157 00840682109666SKN16290004SA SKN16290004SA 2092670-001-510854 00840682109666SKN17090034SA SKN17090034SA 2092670-001-510854 00840682109666SKN17270013SA SKN17270013SA 2092670-001-510854 00840682109666SKN17270014SA SKN17270014SA 2092670-001-516138 00840682109666SKN16440004SA SKN16440004SA 2092670-001-516138 00840682109666SKN16440005SA SKN16440005SA 2092670-001-516138 00840682109666SKN17130042SA SKN17130042SA 2092670-001-516138 00840682109666SKN17130076SA SKN17130076SA 2092670-001-516138 00840682109666SKN17130082SA SKN17130082SA 2092670-001-516138 00840682109666SKN16440003SA SKN16440003SA 2092670-001-516138 00840682109666SKN17200095SA SKN17200095SA 2092670-001-516138 00840682109666SKN17210183SA SKN17210183SA 2092670-001-516138 00840682109666SKN17210184SA SKN17210184SA 2092670-001-516138 00840682109666SKN17300018SA SKN17300018SA 2092670-001-516

code_info

Model, Catalogue, or Code/ UDI/ Mfg. Lot or Serial Number Model, Catalogue or Code # UDI # Mfg. Lot or Serial # 20…

Model, Catalogue, or Code/ UDI/ Mfg. Lot or Serial Number Model, Catalogue or Code # UDI # Mfg. Lot or Serial # 2092670-001-510157 00840682109666SKN16290004SA SKN16290004SA 2092670-001-510854 00840682109666SKN17090034SA SKN17090034SA 2092670-001-510854 00840682109666SKN17270013SA SKN17270013SA 2092670-001-510854 00840682109666SKN17270014SA SKN17270014SA 2092670-001-516138 00840682109666SKN16440004SA SKN16440004SA 2092670-001-516138 00840682109666SKN16440005SA SKN16440005SA 2092670-001-516138 00840682109666SKN17130042SA SKN17130042SA 2092670-001-516138 00840682109666SKN17130076SA SKN17130076SA 2092670-001-516138 00840682109666SKN17130082SA SKN17130082SA 2092670-001-516138 00840682109666SKN16440003SA SKN16440003SA 2092670-001-516138 00840682109666SKN17200095SA SKN17200095SA 2092670-001-516138 00840682109666SKN17210183SA SKN17210183SA 2092670-001-516138 00840682109666SKN17210184SA SKN17210184SA 2092670-001-516138 00840682109666SKN17300018SA SKN17300018SA 2092670-001-516

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0487-2018%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.