The list below contains Medical Device’s Field Corrective Action for the month of March 2025. This list provides field corrective action reporting information to MDA by establishment in accordance to requirement stipulated in Section 41, Act 737 and Regulation 6 of Medical Device (Duties and Obligations of Establishment) Regulations 2019.

Field Corrective Action (FCA) is part of a post-marketing risk assessment measure to ensure the continued safe use of medical devices in the Malaysia market. It is a corrective or preventive action in relation to a medical device which may include –

  • The return of the medical device to the establishment;
  • Modification of the medical device;
  • Exchange of the medical device;
  • Destruction of medical device; or
  • Specific advice on the use of the medical device. 

If you have experienced any safety and performance issue with one of the medical devices listed for FCA action, please seek advice from your medical device authorised representative as soon as possible.

No

Date Received

Title of FCA

Affected Medical Device

MDA Reference Number

MDA Registration Number

Establishment Details

1.

04/03/2025

Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000) – Potential Security Vulnerability

CENTRICITY UNIVERSAL VIEWER

MDA/FCA/P1205-78828863-2025

GB6437620-46699

GE HEALTHCARE SDN. BHD

premarket.my@ge.com

2.

07/03/2025

FA-25022- DxC 500i Clinical Analyzer- Beckman Coulter has determined that the system cannot recalculate a calculated result when results are rerun within the calculated test

DxC 500i AU Chemistry Module

MDA/FCA/P1209-84718400-2025

IVDA8913224-171351

BECKMAN COULTER MALAYSIA SDN. BHD.

song01@beckman.com

3.

11/03/2025

FA-AM-FEB2025-305: Alinity m System Software Upgrade 1.9.0

ALINITY M SYSTEM

MDA/FCA/P1217-81246151-2025

IVDB7120020-41682

ABBOTT LABORATORIES (MALAYSIA) SDN. BHD.

khenghoe.kwa@abbott.com

4.

11/03/2025

FA1482 NIM Vital Stimulus Artifact

NIM VITAL SYSTEM

MDA/FCA/P1218-98649608-2025

GB4580925-195936

MEDTRONIC MALAYSIA SDN BHD

simon.yam@medtronic.com

5.

12/03/2025

Discrepancies and Insufficiencies in Markings and Symbols in the User Manual, Rating Label, and Cuff of the NovoPlus Neuw Upper Arm Blood Pressure Monitor NBP100

UPPER ARM BLOOD PRESSURE MONITOR

MDA/FCA/P1215-22764825-2025

GB10141423-121141

REVO HEALTHCARE SDN BHD

revohealthcare@yahoo.com

6.

12/03/2025

Raw material specification for ImmunoCAP Allergen f279, Chilipepper (14-5062-01) has not been followed

PHADIA AB IMMUNOCAP™ SPECIFIC IGE

MDA/FCA/P1220-77969806-2025

IVDB2215723-122106

BIOMARKETING SERVICES (M) SDN BHD

rqa.my@biomedglobal.com

7.

12/03/2025

The VasoView HemoPro Systems VH-4000 and VH-3000-W may experience fluid ingress into the handle, potentially affecting the electrical and mechanical function of the tool.

ENDOSCOPIC VESSEL HARVESTING SYSTEM

MDA/FCA/P1221-70903560-2025

GC68111180517

RBD HEALTHCARE SDN BHD

sookpei@rbdhealthcare.com

8.

13/03/2025

The installation instructions for Intermediate Ceiling Construction (Article No. 89-960-12-04), part of the operating theatre lighting system, contain incorrect tightening torques, though the component itself has no clinical function.

OPERATING LIGHT

MDA/FCA/P1219-77992789-2025

GMD96238811718A

KLS MARTIN SE ASIA SDN BHD

Gilles.Waeldin@klsmartin.com

9.

13/03/2025

Important safety information has been issued for the Vasoview Hemopro 2 Endoscopic Vessel Harvesting (EVH) System due to complaints about two failure modes: 1) bent or detached heater wire, and 2) silicone peeling or detaching from the jaws of the harvesting tool.

ENDOSCOPIC VESSEL HARVESTING SYSTEM

MDA/FCA/P1224-89394131-2025

GC68111180517

RBD HEALTHCARE SDN BHD

sookpei@rbdhealthcare.com

10.

13/03/2025

Important Product Information: Durashock Blood Pressure Device - Storage Testing Failure for Leaks and Accuracy

Welch Allyn Blood Pressure Gauges

MDA/FCA/P1225-19484240-2025

GA7214422-88069

WELCH ALLYN MALAYSIA SDN BHD

 jason_lee@baxter.com

11.

13/03/2025

Important Product Information: Durashock Blood Pressure Device - Storage Testing Failure for Leaks and Accuracy

Welch Allyn 767 Blood Pressure Gauges

MDA/FCA/P1226-51944182-2025

GA2325622-90637

12.

14/03/2025

020 FSCA ACHC 24-07, Incorrect Software Flagging for the Atellica CH Revised C Reactive Protein (RCRP) Assay

ATELLICA® CH REVISED C‑REACTIVE PROTEIN (RCRP)

MDA/FCA/P1228-57747534-2025

IVDB10942623-142160

SIEMENS HEALTHCARE SDN. BHD.

aili.siow@siemens-healthineers.com

13.

17/03/2025

ABL90 FLEX analyzer unexpected “freeze” and restart

ABL90 FLEX

MDA/FCA/P1214-41883730-2025

IVDC5590952317

RADIOMETER MALAYSIA SDN. BHD.

ahila.padmanathan@radiometer.my

14.

17/03/2025

Xlung Kit 230 leakages at the recirculation port

NOVALUNG KITS

MDA/FCA/P1227-56476376-2025

GD7111223-118844

MEGSHER MEDIC (M) SDN BHD

megsher.info@gmail.com

15.

19/03/2025

An issue in the CELL-DYN Ruby system where, when expired reagents are scanned or manually entered, the system will change the expiration date to current or future date.

CELL-DYN RUBY

MDA/FCA/P1230-86263341-2025

IVDB9465823-115114

ABBOTT LABORATORIES (MALAYSIA) SDN. BHD.

khenghoe.kwa@abbott.com

16.

19/03/2025

FA-25023- DxC 500 AU Clinical Chemistry Analyzer may not run a requested calibration order for a two-part reagent and subsequently prevents any new calibration order from being placed.

DxC 500 AU Clinical Chemistry Analyzer

MDA/FCA/P1231-72045130-2025

IVDA3952124-168118

BECKMAN COULTER MALAYSIA SDN. BHD.

song01@beckman.com

17.

19/03/2025

FA-25025-DxC 500i Clinical Analyzer may not run a requested calibration order for a two-part reagent and subsequently prevents any new calibration order from being placed.

DxC 500i AU Chemistry Module

MDA/FCA/P1232-91158167-2025

IVDA8913224-171351

18.

19/03/2025

FA-25026- DxC 500i Clinical Analyzer - Information within the APF (Assay Protocol File) will load decimal numerals as whole numbers (example 1.25 will load as 125).

DxC 500i AU Chemistry Module

MDA/FCA/P1232-71645655-2025

IVDA8913224-171351

19.

20/03/2025

Venue Go, Venue Fit - Battery for certain Venue Go and Venue Fit ultrasound systems with software versions R2, R3, and R4 can potentially develop an internal failure which could result in smoke or fire.

VENUE GO ULTRASOUND SYSTEM

MDA/FCA/P1235-72426775-2025

GB120001319219

GE HEALTHCARE SDN. BHD

premarket.my@ge.com

20.

21/03/2025

Centricity High Acuity Critical Care (CHA CC) and Centricity High Acuity Anesthesia (CHA A) - potential issue within the CHA Order module’s Edit Order window.

CENTRICITY HIGH ACUITY ANESTHESIA

MDA/FCA/P1241-76380635-2025

GMD29146275517A

21.

21/03/2025

FA-25027- If a DxI 9000 analyzer has accumulated canceled QC test results that were not sent to the host system, the analyzer may lose communication with the host system. The lost connection cannot be restored by routine troubleshooting.

ACCESS UNCONJUGATED ESTRIOL

MDA/FCA/P1242-37020681-2025

IVDB2555024-162080

BECKMAN COULTER MALAYSIA SDN. BHD.

song01@beckman.com

22.

24/03/2025

SY052/21/S (CSAN) - RT Image Suite Saving Issue

SYNGO.VIA VB30

MDA/FCA/P1239-63380128-2025

GB120001319219

SIEMENS HEALTHCARE SDN. BHD.

aili.siow@siemens-healthineers.com

23.

24/03/2025

FA-AM-MAR2025-306 Alinity m System Drawer Design

ALINITY M SYSTEM

MDA/FCA/P1243-70007271-2025

IVDB7120020-41682

ABBOTT LABORATORIES (MALAYSIA) SDN. BHD.

khenghoe.kwa@abbott.com

24.

25/03/2025

021 FSCA POC 25-007 epoc BGEM Test Card | Epoc Discrepant High pH Results with Sensor Configuration 45.n

EPOC BLOOD ANALYSIS SYSTEM

MDA/FCA/P1244-53368799-2025

IVDC7557621-75750

SIEMENS HEALTHCARE SDN. BHD

aili.siow@siemens-healthineers.com

25.

25/03/2025

022 FSCA ACHC 24-07 Follow Up Atellica CH Revised C-Reactive Protein (RCRP) | Incorrect Software Flagging for the Atellica CH Revised C Reactive Protein (RCRP) Assay

ATELLICA® CH REVISED C‑REACTIVE PROTEIN (RCRP)

MDA/FCA/P1245-61271022-2025

IVDB10942623-142160

26.

26/03/2025

FA1263 EverFlex Self-Expanding Peripheral Stent with Entrust Delivery System Instructions for Use Updates

EVERFLEX SELF-EXPANDING PERIPHERAL STENT WITH ENTRUST DELIVERY SYSTEM

MDA/FCA/P1246-84903910-2025

GC2869522-88521

MEDTRONIC MALAYSIA SDN BHD

simon.yam@medtronic.com