Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 20837 |
| Brand Name: | Teleflex Athlone - OnControl Bone Marrow Systems |
| Model: | |
| Affected: | Catalogue numbers: 9403-EU-006, 9408-EU-006, 9411-EU-006, 9462-EU-001, 9463-EU-001, 9464-EU-001, 9466-EU-001 |
| Software version: | |
| Recalling Organisation: | Teleflex Medical New Zealand OFFICE 011, 110 CARLTON GORE ROAD Newmarket Auckland 1023 |
| Contact Information: | 027 476 4009 |
| Manufacturer: | Teleflex Medical Europe Ltd |
| Issue: | Due to the compromised packaging, the sterility of the inside drape, which is used in preparation for bone marrow aspiration with the OnControl system, cannot be guaranteed. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 18/11/2016 |
