Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 26353 |
| Brand Name: | Mortara Cable/lead, electrocardiograph |
| Model: | |
| Affected: | Multiple part numbers |
| Software version: | |
| Recalling Organisation: | Ebos Group Ltd 108 Wrights Road Addington Christchurch |
| Contact Information: | 0800 18 17 16 |
| Manufacturer: | Mortara Instruments Inc |
| Brand Name: | Cable/lead, electrocardiograph |
| Model: | |
| Affected: | Multiple part numbers |
| Software version: | |
| Recalling Organisation: | Ebos Group Ltd 108 Wrights Road Addington Christchurch |
| Contact Information: | 0800 18 17 16 |
| Manufacturer: | Welch Allyn Inc |
| Brand Name: | Mortara ECG |
| Model: | |
| Affected: | Multiple part numbers |
| Software version: | |
| Recalling Organisation: | Ebos Group Ltd 108 Wrights Road Addington Christchurch |
| Contact Information: | 0800 18 17 16 |
| Manufacturer: | Mortara Instruments Inc |
| Brand Name: | Electrocardiograph, general purpose |
| Model: | |
| Affected: | Multiple part numbers |
| Software version: | |
| Recalling Organisation: | Ebos Group Ltd 108 Wrights Road Addington Christchurch |
| Contact Information: | 0800 18 17 16 |
| Manufacturer: | Welch Allyn Inc |
| Issue: | The manufacturer has become aware from internal testing that impacted Welch Allyn-branded and Mortara-branded products may not meet the "Defibrillation Withstand" requirements of EN/IEC 60601-2-25 Medical Electrical Equipment. These are particular requirements for the Safety of Electrocardiographs, a standard the product claims to meet. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 5/8/2020 |
