Straumann Pty Ltd - Cerabone Granules and Mucoderm (multiple sizes) Recall

A recall notice for Cerabone Granules and Mucoderm (multiple sizes) supplied by Straumann Pty Ltd as the product’s patient information leaflet and patient implant card have been left out when the products were supplied.

The implantation card and patient information sheet provide traceability of the products and important safety information for the patient.

Straumann Pty Ltd - Cerabone Granules and Mucoderm (multiple sizes)

PRA number

2021/19186

Published date

8 Sep 2021

Product description

Cerabone Granules (multiple sizes) and
Mucoderm (multiple sizes)

Product numbers: BO-1510, BO-1511, BO-1512, BO-1515, BO-1520, BO-1521, BO-1522, BO-1525, BO-701520, BO-702030 and BO-703040

All lot numbers supplied since 1 December 2020

ARTG 329433
(Straumann Pty Ltd - cerabone granulate - Dental bone matrix implant, animal-derived)

ARTG 353073
(Straumann Pty Ltd - mucoderm - Collagen dental regeneration membrane)

What are the defects?

The product’s patient information leaflet and patient implant card have been left out when the products were supplied.

The implantation card and patient information sheet provide traceability of the products and important safety information for the patient.

What are the hazards?

Patients who have been supplied the products without the correct patient information, may not be aware of important information about the use of the product and this poses an increased risk of adverse health complications.

What should consumers do?

Consumers will be contacted by Straumann and provided with an updated patient implant card and patient information leaflet.

For more information, contact Straumann on 03 9261 1300.

Supplier

Straumann Pty Ltd

Traders who sold this product

Hospitals and dental care centres

Where the product was sold

New South Wales

Queensland

South Australia

Tasmania

Victoria

Australian Capital Territory

Dates available for sale

1 Dec 2020 - 1 Sep 2021

Responsible regulator

Therapeutic Goods Administration is the responsible regulator for this recall.

Product category

Pharmacy

Personal