Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 26008 |
| Brand Name: | Natus - Electroencephalograph |
| Model: | |
| Affected: | Data Acquisition Box (DAB with part number OBM00002) |
| Software version: | |
| Recalling Organisation: | Paragon Medical Ltd t/a LR Instruments and Scanmedics Immulab & Insight Surgical Level 2 Bldg. 5 60 Highbrook Drive East Tamaki Auckland 2013 |
| Contact Information: | 0800 150 030 |
| Manufacturer: | Natus Medical Incorporated (XLTEK) |
| Issue: | During manufacture of the OBM systems it was discovered that the system functional test (impedance and noise) was not carried out on the affected items prior to release to the customer. The manufacturer cannot attest to the system functionality of the affected items. |
| Recall action type: | Recall |
| Recall action: | Product to be exchanged |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 7/5/2020 |
