| Type of Product |
Medical Device |
| TGA Recall Reference |
RC-2014-RN-00454-1 |
| Product Name/Description |
Mueller Hinton-HTM (culture media). An in vitro diagnostic medical device (IVD)
Batch Number: 1294381
ARTG Number: 214128 |
| Recall Action Level |
Hospital |
| Recall Action Classification |
Class II |
| Recall Action Commencement Date |
17/04/2014 |
| Responsible Entity |
|
| Reason/Issue |
An investigation by the manufacturing site has revealed that some plates within this batch may fail to grow Haemophilus influenza. |
| Recall Action |
Recall |
| Recall Action Instructions |
Thermo Fisher is requesting their customers to discontinue use and destroy the affected batch of Mueller Hinton -HTM. |
| Contact Information |
1800 331 163 - Oxoid Australia |