Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 29796 |
| Brand Name: | ECHOTIP® ULTRA Endoscopic Ultrasound Needle |
| Model: | CK-ECHO-19, G31520: ECHOTIP ENDOSCOPIC ULTRASOUND NEEDLE 19G. CK-ECHO-1-22, G31518 : ECHOTIP ENDOSCOPIC ULTRASOUND NEEDLE 22G. CK-ECHO-22-F, G03793: ECHOTIP FIDUCIAL NEEDLE 22G. |
| Affected: | |
| Software version: | |
| Recalling Organisation: | Obex Medical Ltd Level 3, 109 Carlton Gore Road Newmarket Auckland 1023 |
| Contact Information: | 0800 656 539 |
| Manufacturer: | Cook Ireland Ltd |
| Issue: | The manufacturer has implemented an IFU update for the Echo-Tip Ultra Endoscopic Ultrasound Needle. There is no change to the manufacturing process, device, or design. This change does not affect the quality, safety, or effectiveness of the device. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 9/8/2022 |
