The list below contains Medical Device’s Field Corrective Action for the month of August 2022. 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.

 

Date received

Title of FCA

Affected

Medical Device

MDA Reference Number

MDA Registration Number

Description

Local Establishment

Contact Detail

4 August 2022

 FCA Notification on a potential performance issue found in the Alinity ci-series software versions 3.3.3 and lower.

Alinity ci-series System Control Module (SCM)

MDA/FCA/2022-P127

IVDA3247720-46201

Abbott has identified a potential performance issue found in the Alinity ci-series software versions 3.3.3 and lower. Abbott is releasing Alinity ci-series software version 3.4.0 to correct this issue

Farah Syuhaidah binti Ahmad Jahiddin

Regulatory Affairs & Quality Assurance Executive

Abbott Laboratories (M) Sdn. Bhd.

10 August 2022

FCA Notification on  Immunoassay Speciality Control Level 1, 2 and 3 - stability period is shortened from 1 day to 8 hours

Randox Immunoassay Speciality Control Level 1, 2 and 3

MDA/FCA/2022-P128

IVD79016125118

Low risk as stability period is shortened from 1 day to 8 hours

Mark Ong,

Biorex Mannheim Malaysia Sdn Bhd

12 Sept 2022

 Field Corrective Action on BinaxNOW Nasopharyngeal Swab Pack

BINAXNOW RSV CARD

MDA/FCA/P0005-82380934-2022

IVDC21199341118

 Missing the supplementary local label that Medical Device Authority (MDA) requires. The subject label contains the Name, Address and the COnntact Number of Authorised Representative and the MDA Registration Number.

Law Ching Yee

Regulatory Affairs & Compliance Manager

Abbott Medical (Malaysia) Sdn. Bhd

18 August 2022

 Assurity & Endurity Laser Adhesion Preparation Field Safety Corrective Action (FA-Q322-CRM-1)

ASSURITY & ASSURITY MRI PACEMAKERS

MDA/FCA/P0028-14319524-2022

GD71875822118

Abbott is informing clinicians of the potential for device malfunction which may affect a specific subset of serial numbers of AssurityTM and EndurityTM pacemakers.

Law Ching Yee

Regulatory Affairs & Compliance Manager

Abbott Medical (Malaysia) Sdn. Bhd.

3 August 2022

 FA09JUN2022 ARCHITECT Hemoglobin A1c (A1c) and Alinity c Hemoglobin A1c

HEMOGLOBIN A1C

MDA/FCA/PX0036-57022116-2022

IVDB24013273018

Internal data analysis found that for ARCHITECT HbA1c, LN 04P52-20, and Alinity c HbA1c, LN 08P4320 and 08P4377, when the Total Hemoglobin concentration is to be erratic when analyzing whole blood or hemolysate samples with poor sample integrity, due to micro-clots and particulate matter, associated with low Total Hemoglobin values.

VIOLA SUBHASHINI PETERS

REGULATORY AFFAIRS & QUALITY ASSURANCE MANAGER

ABBOTT LABORATORIES (MALAYSIA) SDN. BHD.

3 August 2022

 FA09JUN2022 ARCHITECT Hemoglobin A1c (A1c) and Alinity c Hemoglobin A1c

ALINITY C HBA1C

MDA/FCA/PX0038-15790437-2022

IVDB6127219-28113

Internal data analysis found that for ARCHITECT HbA1c, LN 04P52-20, and Alinity c HbA1c, LN 08P4320 and 08P4377, when the Total Hemoglobin concentration is <1250 μmol/L there is a potential for the reported %HbA1c to be erratic when analyzing whole blood or hemolysate samples with poor sample integrity, due to micro-clots and particulate matter, associated with low Total Hemoglobin values.

VIOLA SUBHASHINI PETERS

REGULATORY AFFAIRS & QUALITY ASSURANCE MANAGER

ABBOTT LABORATORIES (MALAYSIA) SDN. BHD.

8 August 2022

 Field Action Information Package: FA Number DX, FA-22024, iChemVELOCITY Strips, PN 800-7204, Lot #7204612M

ICHEM VELOCITY URINE CHEMISTRY SYSTEM

MDA/FCA/P0030-67757121-2022

IVDB33139176018

A strip lot number result for Nitrite was overestimated (high) and the result for Leukocyte Esterase was underestimated (low) on quality control (QC) samples with lot 7204612M. Customer retested QC, and QC passed during retest and customer ran patient samples. Erroneous patient results were generated.

NUR AISHAH BINTI ABD AZIZ

RA SPECIALIST

BECKMAN COULTER MALAYSIA SDN. BHD.

25 August 2022

 IMMAGE Immunochemistry Systems Rheumatoid Factor (RF) Reagent

IMMAGE RHEUMATOID-INFLAMMATORY DISEASE MARKERS

MDA/FCA/P0067-37877392-2022

IVDB93928233618

Extremely high RF concentrations (> 6,000 IU/mL) in serum may result in an antigen excess condition producing a low RF value on the IMMAGE System.

NUR AISHAH BINTI ABD AZIZ

RA SPECIALIST

BECKMAN COULTER MALAYSIA SDN. BHD.

29 August 2022

 Automatic samples approval issue with Phadia 200 instrument.

PHADIA INSTRUMENTS

MDA/FCA/P0061-39015744-2022

IVDA1670544317

An issue has been found when the Phadia 200 Software has the setting “Automatic approval by each available result” and the Curve Control (CC) for an EliA assay run is not OK. This combination can lead to samples being approved without an OK Curve Control for the assay run.

APPHIA EU CHIA HUI

SENIOR REGULATORY & QA

BIOMARKETING SERVICES (M) SDN BHD

24 August 2022

 

Bearing pin might come loose and Patient Seat of the Unit might

swivel back

 

DENTAL TREATMENT CHAIR TENEO

MDA/FCA/P0065-92992143-2022

GB8397719-30974

A spot check investigation within the affected population the market, initiated after issue 8000573478

showed that there were 5 of 20 devices where this bearing pin has moved out of its original position. The movement of that bearing pin in one direction is uncritical, because of an internal stop plate.

SITI SARA BINTI MOHAMED

REGULATORY AFFAIRS MANAGER

DENTSPLY SIRONA MALAYSIA SDN. BHD.

22 August 2022

 NexSys® PCS (1.4.2 and earlier)- Interruption during "Smart Last Cycle"

PCS®300 PLASMA COLLECTION SYSTEM (NEXSYS PCS™)

MDA/FCA/P0010-18518824-2022

GC5412720-49541

This software defect, under certain conditions, can affect the calculation of estimated Red Blood Cell (RBC) Loss and the associated system flags, when a “Smart Last Cycle” is interrupted.

CHENG CHIN YEE

SENIOR REGULATORY AFFAIRS SPECIALIST

HAEMONETICS MALAYSIA SDN. BHD.

21 August 2022

 FA1243 Phase III Pump Inner Bearing Demagnetization - Investigation Update

HEARTWARE VENTRICULAR ASSIST SYSTEM (HVAD)

MDA/FCA/P0024-87946717-2022

GD74345985518

Three (3) complaints (see below) have been identified where the magnets inside the center post of the HVAD pump corroded causing the pump impeller to rotate non-concentrically and contact the center post inside the pump. All 3 cases had high watt alarms which led to a pump exchange.

LEE YOUN YOUN

REGULATORY AFFAIRS LEAD

MEDTRONIC MALAYSIA SDN BHD

17 August 2022

 FA1204 Phase II Synergy Cranial (9733763) and StealthStation Cranial (9735585) Biopsy Depth Gauge Cycle View Inaccuracy

STEALTHSTATION S7 TREATMENT GUIDANCE SYSTEM (CRANIAL)

MDA/FCA/P0055-73877537-2022

GD86373862018

If the user encounters the software anomaly where the graphical Biopsy Depth Gauge is no longer synchronized with other navigation views, there is the potential to navigate the biopsy needle too shallow or deep to target. This issue can potentially lead to resection of normal brain tissue or eloquent anatomical regions of the brain.

LEE YOUN YOUN

REGULATORY AFFAIRS LEAD

MEDTRONIC MALAYSIA SDN BHD

8 August 2022

 

BiPAP A30, BiPAP A40 and OmniLab Advanced+

Motor Stator Material Non-Conformance

 

BIPAP A40 VENTILATOR

MDA/FCA/P0045-76195787-2022

GC65940156417

Philips Respironics determined that certain devices were built with motor assemblies that could contain non-conforming plastic material. If the non-conforming plastic is present in the device motor, it could lead to off-gassing and structural failure causing the immediate and sudden failure of the device during use.

ZAM ZARINA BINTI MAT ALI

Q&R MANAGER

PHILIPS MALAYSIA SDN BERHAD

12 August 2022

MEDICAL DEVICE - FIELD NOTIFICATION

 

STERRAD 100NX STERILIZATION SYSTEM

(Parts: 10104, 10104-002, 10104-003, 10104-004)

STERRAD 100NX STERILIZATION SYSTEM WITH ALL CLEAR TECHNOLOGY

(Parts: 10104-005, 10104-006, 10104-007, 10104-008)

 

ASP STERRAD 100NX STERILIZATION SYSTEM

MDA/FCA/P0049-45627563-2022

GC15247682318

 ASP has determined certain STERRAD 100NX Sterilization Systems may exceed the CISPR 11 Group 1, Class A radiated emissions limits as set forth in international electrotechnical standard, IEC 60601-1-2: Medical Electrical Equipment - Electromagnetic Compatibility - Requirements and Tests.

FOO YOON MEE

ACCOUNT MANAGER

RAPHA MEDICAL SDN. BHD.

24 August 2022

 PP 22-003 N Antiserum to Human IgG

IMMUNOGLOBULINS

MDA/FCA/P0062-22213860-2022

IVDB52967131318

Siemens Healthcare Diagnostics Products GmbH has confirmed that the N Antiserum to Human IgG lots mentioned above are not meeting the current High-Dose Hook Effect expectation given in the Instructions for Use (IFU) for the urine and CSF sample material.

LAM YEN LI

HEAD OF QUALITY & TECHNOLOGY

SIEMENS HEALTHCARE SDN BHD

15 July 2022

 PP 22-001

IMMUNOGLOBULINS (N LATEX FLC KAPPA AND N LATEX FLC LAMBDA)

MDA/FCA/P0008-87189324-2022

IVDB6883521-63634

Siemens Healthcare Diagnostics Products GmbH has confirmed that customers may experience an increased rate (average flagging rate: 6%) of flagged FLC LAMBDA Quality Control (QC) and patient sample results when using this assay on the Atellica CH 930 Analyzer.

LAM YEN LI

HEAD OF QUALITY & TECHNOLOGY

SIEMENS HEALTHCARE SDN BHD

5 August 2022

 

CT017/22/S for P81/82

Providing MS hotfix, bug fixing and workflow improvement for

software VA40A with service pack 2

 

SOMATOM GO.TOP

MDA/FCA/P0040-47741375-2022

GC110591186618

CT017/22/S for P81/82

Providing MS hotfix, bug fixing and workflow improvement for software VA40A with service pack 2

LAM YEN LI

HEAD OF QUALITY & TECHNOLOGY

SIEMENS HEALTHCARE SDN BHD

9 August 2022

 CT008/22/S - Software version VA30A_SP5 on CT products

SOMATOM GO.TOP

MDA/FCA/P0047-52243946-2022

GC110591186618

Some technical issues have been identified in software version syngo CT VA30A SP4, and these issues may result in sporadic problems causing scanning workflow interruptions, unexpected user notifications and image artifacts. Sporadic software errors may also occur during interventional workflows.

LAM YEN LI

HEAD OF QUALITY & TECHNOLOGY

SIEMENS HEALTHCARE SDN BHD

23 August 2022

 AX028/22/S - Issue in the tube's error detection mechanism

ARTIS Q

MDA/FCA/P0054-87246920-2022

GC98740520118

The Artis system is provided with a dedicated error detection mechanism. In rare cases of failure of this error detection mechanism it will not be possible to release X‐ray anymore until system shutdown

LAM YEN LI

HEAD OF QUALITY & TECHNOLOGY

SIEMENS HEALTHCARE SDN BHD

1 Sept 2022

 HAMILTON-C6 ventilator - Loose status indicator board

MEDICAL VENTILATOR

MDA/FCA/P0015-76118627-2022

GC25545945118

The defective contact results in a detected technical fault. The two sequences of events can be summarized as follows:

1. the status indicator board may become loose

2.water ingress may lead to oxidation

3.Loose contact is detected as technical faukt multiple times within a very short time

4.An overflow of flog entries of TE 246041 (taLLS_alarmLedError) force the ventilator into "Safety ventilation" or "Ambient state with Panel connection lost message displaye

NUR DIANA ABD RAZAK

HEAD OF QUALITY ASSURANCE

STAR MEDIK SDN BHD

1 Sept 2022

 Temporary Failure of the Hamilton-C6 ventilator display

MEDICAL VENTILATOR

MDA/FCA/P0068-40052483-2022

GC25545945118

Failure of the backlight on the screen (to 2-3 seconds) of the HAMILTON-C6 with potential cause of confusion of the proper application of the ventilator. Issue reported through customer complaint to Hamilton Medical AG and reported to Swissmedic.

NUR DIANA ABD RAZAK

HEAD OF QUALITY ASSURANCE

STAR MEDIK SDN BHD

22 August 2022

 

PRODUCT CORRECTION NOTIFICATION - Report Submitted per to 21 CFR 806

(Report Reference Number 3010939897-04/28/22-001-R)

 

QMS TACROLIMUS IMMUNOASSAY

MDA/FCA/P0052-82522298-2022

IVDC72318308018

Microgenics Corporation has identified QMS® Tacrolimus Calibrator, catalog number 10015573, lot numbers 74267412, 74175462, 74085025, 73925326, 73767734 and 73712031 are recovering between 85 – 93% of their target values, resulting in over-quantitation in tacrolimus patient result values when used with the QMS® Tacrolimus Immunoassay.

EIK LEE FANG

QUALITY SYSTEMS MANAGER

DIAGNOSTIC SYSTEMS (M) SDN. BHD.