Type of Product |
Medical Device |
TGA Recall Reference |
RC-2017-RN-01018-1 |
Product Name/Description |
Covidien Emprint Percutaneous Antennas with Thermosphere Technology
Emprint Percutaneous Antenna with Thermosphere Technology, Short (15cm) Item Code: CA15L1
Emprint Percutaneous Antenna with Thermosphere Technology, Standard (20cm) Item Code: CA20L1
Emprint Percutaneous Antenna with Thermosphere Technology, Long (30cm) Item Code: CA30L1
Lot Numbers beginning with S5L through S7G
Expiration: November 2017 through July 2019
ARTG Number: 178369 |
Recall Action Level |
Hospital |
Recall Action Classification |
Class I |
Recall Action Commencement Date |
10/08/2017 |
Responsible Entity |
|
Reason/Issue |
Medtronic have received reports that the ceramic trocar tip of the Emprint ablation antenna is disengaging from the needle shaft post-ablation. Tip disengagement can result in the ceramic trocar tip remaining in the patient presenting a risk of latent migration and potential damage to adjacent tissue. Four of the complaint reports indicate that the trocar tip was not retrieved. |
Recall Action |
Recall |
Recall Action Instructions |
Medtronic is requesting customers: 1.Quarantine and discontinue use of the specified item codes and lots; 2.Immediately advise all surgeons/surgery personnel of this recall; 3. Check if their facility has distributed the affected products to other persons or facilities, if so, please promptly forward a copy of this letter to those recipients; 4. Email the completed Recall Response Form supplied with the customer letter to Medtronic's Regulatory Affairs Department at ANZ.Recalls@covidien.com or fax to 02 8904 8798. Please include a copy of the Recall Response Form with the returned units; and 5. Label the goods with the provided (ZRE#) for easy identification. Do not return goods without the corresponding ZRE# provided by Medtronic.
This action has been closed out on 14/02/2019 |
Contact Information |
02 9429 3179 - Medtronic |