Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 24062 |
| Brand Name: | Cook Urological Dilator, Endotherapy |
| Model: | |
| Affected: | specific lots |
| Software version: | |
| Recalling Organisation: | Obex Medical Ltd Level 3, 109 Carlton Gore Road Newmarket Auckland 1023 |
| Contact Information: | 0800 656 539 |
| Manufacturer: | Cook Incorporated |
| Brand Name: | Urology Wire Guide |
| Model: | |
| Affected: | specific lots |
| Software version: | |
| Recalling Organisation: | Obex Medical Ltd Level 3, 109 Carlton Gore Road Newmarket Auckland 1023 |
| Contact Information: | 0800 656 539 |
| Manufacturer: | Cook Incorporated |
| Brand Name: | Cook Urological Ureteral Stent |
| Model: | |
| Affected: | specific lots |
| Software version: | |
| Recalling Organisation: | Obex Medical Ltd Level 3, 109 Carlton Gore Road Newmarket Auckland 1023 |
| Contact Information: | 0800 656 539 |
| Manufacturer: | Cook Incorporated |
| Brand Name: | Cook Urological Dilator, Urinary Duct |
| Model: | |
| Affected: | specific lots |
| Software version: | |
| Recalling Organisation: | Obex Medical Ltd Level 3, 109 Carlton Gore Road Newmarket Auckland 1023 |
| Contact Information: | 0800 656 539 |
| Manufacturer: | Cook Incorporated |
| Issue: | The manufacturer has identified that the affected lots may contain a wire guide that was incorrectly loaded into the wire guide holder. This could lead to the stiff tip of the wire guide being introduced into the patient instead of the flexible tip. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Wholesale |
| Date Commenced: | 10/1/2019 |
