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Medifab Ltd - DM36 Dreama Slim Support Pad for Jenx Dreama Sleep Mattress Recall.18.10.2020

A recall notice for DM36 Dreama Slim Support Pad for Jenx Dreama Sleep Mattress supplied by Medifab Ltd as the inserts that attach the small PU pad to the bracket are manufactured from plywood sheet material that may contain structural defects. This reduces the strength of the fitting, which can result in the plywood splitting and the support pad breaking off the bracket.

Breakage may occur without warning and the affected items cannot be easily identified upon inspection.

Medifab Ltd - DM36 Dreama Slim Support Pad for Jenx Dreama Sleep Mattress

PRA No.

2020/18606

Date published

18 Oct 2020

Product description

DM36 Dreama Slim Support Pad for Jenx Dreama Sleep Mattress

Product Code: 7120-3240-000

Manufactured between November 2019 and September 2020

ARTG 261614
(Medifab Ltd - Positioning aid system)

This product was previously the subject of a recall on 8 July 2020 (PRA2020/18418) for a defect in a different part.

What are the defects?

The inserts that attach the small PU pad to the bracket are manufactured from plywood sheet material that may contain structural defects. This reduces the strength of the fitting, which can result in the plywood splitting and the support pad breaking off the bracket.

Breakage may occur without warning and the affected items cannot be easily identified upon inspection.

What are the hazards?

There is a risk of injury if the affected items breaks while in use.

What should consumers do?

Immediately cease using the affected item. Medifab will contact affected consumers in writing to arrange for replacement part to be fitted.

Only the identified part is required to be removed, any other Dreama system components remain safe for use.

For further information, contact Medifab on 03 6427 0105.

Supplier

Medifab Ltd

Traders who sold this product

Healthcare equipment retailers and mobility and rehabilitation services

Where the product was sold

New South Wales

Victoria

Dates available for sale

  • 1 November 2019 - 30 September 2020

Responsible regulator

Therapeutic Goods Administration is the responsible regulator for this recall.

Product category

Pharmacy

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