Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 14898 |
| Brand Name: | Origio Pasteur Pipette |
| Model: | |
| Affected: | Lots: 651112043, 650812346 |
| Software version: | |
| Recalling Organisation: | Origio Australasia Pty Ltd Unit 31, 7 Sefton Road Thornleigh New South Wales 2120 Australia |
| Contact Information: | |
| Manufacturer: | Origio Inc (MidAtlantic Devices) |
| Issue: | The manufacturer has received a complaint from a customer that 2 specific lots of Pasteur Pipettes have failed the Mouse Embryo Assay (MEA) re-test performed according to their internal MEA test protocols. |
| Recall action type: | Recall |
| Recall action: | Product to be destroyed |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 1/7/2013 |
