The list below contains Medical Device Recalls for the month of May 2024. This list provides recall reporting information to the Malaysian Medical Device Authority (MDA) by establishments in accordance with the requirements stipulated in Section 42, Act 737, and Regulations 7 and 8 of the Medical Device (Duties and Obligations of Establishment) Regulations 2019.

Recall is part of a post-marketing risk assessment measure to ensure the continued safe use of medical devices in the Malaysian market. A recall is any action taken by the establishment of the medical device to remove the medical device from the market or to retrieve the medical device from any person to whom it has been supplied, and to notify affected persons of its defectiveness or potential defectiveness.

If you have experienced any safety or performance issues with one of the medical devices listed for recall action, please seek advice from your healthcare professional as soon as possible.

  MEDICAL DEVICE RECALL LISTING MAY 2024 

Date Received

Reference No.

Recall Type

Product Name

Product Registration

Recall Class

Reason of Recall

Recalling Establishment

Establishment License

06/05/2024

  MDA/Recall/P0271-76917725-2024

Voluntary Recall

HUMIDIFIER MYAIRVO2

GB197511053618               

Class II

A07: Electrical /Electronic Property Problem

EMERGO MALAYSIA SDN. BHD.

MDA-5078-W123

08/05/2024

  MDA/Recall/P0274-20416296-2024

Voluntary Recall

LAPAROSCOPY SYSTEM

GB26809989718               

Class III

A27: Appropriate Term/Code Not Available (require revision_

OLYMPUS (MALAYSIA) SDN. BHD.

MDA-2218-WDP121

14/05/2024

 

  MDA/Recall/P0277-92317170-2024

Voluntary Recall

TACTOSET INJECTABLE BONE SUBSTITUTE SYSTEM

GD5361723-124925

Class II

A25: No Apparent Adverse Event

CIMED HEALTHCARE SDN. BHD.

MDA-3498-W122

15/05/2024

  MDA/Recall/P0278-91305682-2024

Voluntary Recall

PDS™ II (POLYDIOXANONE) STERILE SYNTHETIC, ABSORBABLE SUTURE

GD4349722-103519

Class III

A02: Manufacturing, Packaging or Shipping Problem

JOHNSON & JOHNSON SDN BHD.

MDA-4880-WDP123

15/05/2024

  MDA/Recall/P0279-39693928-2024

Voluntary Recall

CASCADE IOMAX

GC5241323-144670

Class III

A02: Manufacturing, Packaging or Shipping Problem

T T MEDICAL MANAGEMENT SDN. BHD.

MDA-2373-W121

* The information contained in the Medical Device Authority Recall database is released under Regulation 7(8) and Regulation 8 (5) of Malaysia’s Medical Device Regulations 2019.