Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 14113 |
| Brand Name: | Arrow Berman Angiographic Balloon Catheters |
| Model: | Part numbers: AI-07130, AI-07130J, AI-07131, AI-07132, AI-07133, AI-07134, AI-07135, AI-07136, AI-07137, AI-07138 |
| Affected: | All lots |
| Software version: | |
| Recalling Organisation: | InterMed Medical Ltd 71 Apollo Drive Albany AUCKLAND 1311 |
| Contact Information: | 0800 333 444 |
| Manufacturer: | Arrow International Inc |
| Issue: | The manufacturer advises that the labelling for the product numbers listed above formerly referenced Renografin-76 contrast medium (viscosity of 8.4 centipoise), which is no longer available. Arrow is in the process of updating the labelling and Instructions for Use for these products. In the meantime, when choosing an alternative contrast medium, health care providers are instructed to select a contrast medium with a viscosity of 8.4 centipoise or lower for use with the pressure and flow settings specified in the current IFU |
| Recall action type: | Alert |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 22/1/2013 |
