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Type of Product Medical Device
TGA Recall Reference RC-2016-RN-01574-1
Product Name/Description ID-DC Screening II. An in vitro diagnostic medical device (IVD).

Catalogue Number: 004831
Lot Number: 50560.79.04
Expiry Date: 30 Sept 2017

ARTG Number: 220117
Recall Action Level Hospital
Recall Action Classification Class II
Recall Action Commencement Date 12/12/2016
Responsible Entity Bio-Rad Laboratories Pty Ltd
Reason/Issue It has been identified that the box insert of Lot 50560.79.04 may not be the one corresponding to the product.
Recall Action Recall for Product Correction
Recall Action Instructions Bio-Rad is advising customers to discard the box inserts of the affected lot and replace them with the correct box inserts provided.

This action has been closed out on the 29/10/2018.
Contact Information 1800 224 354 - Bio-Rad Laboratories