Database updated: 18 November 2024
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 29343 |
| Brand Name: | ENT - NIM EMG Endotracheal Tubes |
| Model: | ENDOTRACH TUBE 8229506 CONT EMG 6MM ROHS: 8229506; ENDOTRACH TUBE 8229507 CONT EMG 7MM ROHS: 8229507; ENDOTRACH TUBE 8229508 CONT EMG 8MM ROHS: 8229508 |
| Affected: | |
| 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 manufacturer is issuing a follow up to the May 2022 customer letter regarding the use of the NIM™ Standard Reinforced EMG Endotracheal Tube & NIM CONTACT™ Reinforced EMG Endotracheal Tube since updates to the labelling were granted. It is important to carefully review and adhere to the Instructions for Use (IFU) M040175C001DOC1, Rev. C dated 2023-11, as some precautions, warnings and product labels have been added and/or changed. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 12/2/2024 |
