Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 16567 |
| Brand Name: | Arrow PSI Kits, Multi-Lumen/ PSI Kits, CVC/PSI Kits |
| Model: | A-SI-09903-E |
| Affected: | RF3064710, RF3064915 |
| Software version: | |
| Recalling Organisation: | InterMed Medical Ltd 71 Apollo Drive Albany AUCKLAND 1311 |
| Contact Information: | 0800 333 444 |
| Manufacturer: | Arrow International Inc |
| Issue: | Manufacturer is recalling the products die to tip damage noted during internal inspection on the dilator tip of the Percutaneous Sheath Introducer. Tip damage has the potential to result in vessel damage. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 23/4/2014 |
