Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 26077 |
| Brand Name: | Prodimed Arterial Catheters |
| Model: | |
| Affected: | Affected Lot - 50031286 |
| Software version: | |
| Recalling Organisation: | Paragon Care Group New Zealand Limited 69 Elizabeth Knox Place Glen Innes AUCKLAND |
| Contact Information: | 0508 654 258 |
| Manufacturer: | Prodimed SAS |
| Issue: | The manufacturer has identified that during the ethylene oxide sterlisation cycle an undetermined portion of the lot number affected may not have been in contact with ethylene oxide. The sterile state of the products may not be guaranteed. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 2/6/2020 |
