Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 22061 |
| Brand Name: | Draeger IBP module monitoring |
| Model: | |
| Affected: | Dual Hemo MCable Pod |
| Software version: | |
| Recalling Organisation: | Draeger New Zealand Ltd Unit 4 24 Bishop Dunn Place East Tamaki Auckland 2013 |
| Contact Information: | 0800 559 186 |
| Manufacturer: | Draeger Medical Systems Inc |
| Issue: | The manufacturer has determined through internal testing that Dual Hemo MCable Pods with Revision Index (RI) 15 and 16, which are used with the Dräger Infinity Acute Care System, may permit liquid ingress inconsistent with their IPX4 rating, which could potentially result in an incorrect measured value of invasive blood pressure. The corrective action will be completed by December 2107 |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 4/10/2017 |
