| 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 |
|
| 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 |