Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 26228 |
| Brand Name: | BD PosiFlush XS |
| Model: | |
| Affected: | 9192691 |
| Software version: | |
| Recalling Organisation: | Becton Dickinson Ltd Unit 4 / 110 Mays Road Onehunga Auckland 1061 |
| Contact Information: | 0800 572 468 |
| Manufacturer: | BD Medical (USA) |
| Issue: | The manufacturer has identified holes in the packaging, which impacts package integrity and potentially compromises a sterile field. While the sterility of the outer surface of the syringe may be compromised, the saline solution and the sterile path of the syringe are not impacted |
| Recall action type: | Recall |
| Recall action: | |
| Level of recall: | |
| Date Commenced: | 3/7/2020 |
