Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 23041 |
| Brand Name: | MITG - Kit-Laparoscopic Surgical Class IIB |
| Model: | |
| Affected: | Lot numbers - N7L0521KX, N8A0907KX, N8A0146KX, N7L0912KX, N7L0807KX, N7L1038KX, N7L1050KX, N8B0088KX |
| Software version: | |
| Recalling Organisation: | Medtronic New Zealand Limited Unit 16 Mezzanine Level 5 Gloucester Park Road Onehunga AUCKLAND |
| Contact Information: | 0800 377 807 |
| Manufacturer: | Medtronic Australasia Pty Ltd |
| Brand Name: | MITG - Kit- General Surgical Procedure Kit IIAIIB |
| Model: | |
| Affected: | Kit Codes - K8212, K8224, K8257 |
| Software version: | |
| Recalling Organisation: | Medtronic New Zealand Limited Unit 16 Mezzanine Level 5 Gloucester Park Road Onehunga AUCKLAND |
| Contact Information: | 0800 377 807 |
| Manufacturer: | Medtronic Australasia Pty Ltd |
| Issue: | This recall is being conducted due to the potential for a device to be misassembled. Use of a misassembled device may result in failure to form a staple line when tissue is divided, leading to bleeding or leakage of luminal contents. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 29/5/2018 |
