The list below contains Medical Device Recalls for the month of April 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 APRIL 2024 

Date Received

Reference No.

Recall Type

Product Name

Product Registration

Recall Class

Reason of Recall

Recalling Establishment

Establishment License

04/04/2024

  MDA/Recall/P0260-60513733-2024

Voluntary Recall

F&P AIRVO 2 HUMIDIFIER

GB13073385917               

Class II

A07: Electrical /Electronic Property Problem

EMERGO MALAYSIA SDN. BHD.

MDA-5078-W123

09/04/2024

  MDA/Recall/P0261-18637955-2024

Voluntary Recall

COBAS® HCV GT

IVDC84546154618               

Class III

A09: Output Problem

ROCHE DIAGNOSTICS (M) SDN. BHD.

MDA-5585-WDP124

26/04/2024

 

  MDA/Recall/P0263-33396706-2024

Voluntary Recall

ORTHOPAEDIC IMPLANTS

GC86706621718

Class II

A02: Manufacturing, Packaging or Shipping Problem

B. BRAUN MEDICAL INDUSTRIES SDN. BHD.

MDA-4250-W123

30/04/2024

  MDA/Recall/P0270-78379448-2024

Voluntary Recall

ARTIS SYMBIOSE

GC5714520-45735

Class II

A26: Insufficient Information (require revision)

TRANSMEDIC HEALTHCARE SDN. BHD.

MDA-4762-WDP123

* 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.