Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 16378 |
| Brand Name: | Medtronic Endo-Scrub 2 Endoscopic sheath |
| Model: | 1912000, 1912004 |
| Affected: | 113 specific lots manufactured between June 2013 to December 2013 |
| 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 Xomed |
| Brand Name: | Medtronic Endoscope Tubing Set |
| Model: | 1912030 |
| Affected: | 45 specific lots manufactured between June 2013 to December 2013 |
| 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 Xomed |
| Issue: | The luer connector on the end of the tubing that attaches to the sheath may break off, either prior to or during use. Once the connector breaks, the flow of saline to the sheath either ceases or is reduced and leakage occurs at the fracture site. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Healthcare Professional |
| Date Commenced: | 17/3/2014 |
