Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 17792 |
| Brand Name: | Stryker Laproscopic Instruments |
| Model: | Item Numbers: 0250080204, 0250080233, 0250080234, 0250080341, 0250080342, 0250080340 |
| Affected: | All lots |
| Software version: | |
| Recalling Organisation: | Stryker New Zealand Ltd 515 Mount Wellington Highway Mount Wellington AUCKLAND 1060 |
| Contact Information: | 0800 787 9287 |
| Manufacturer: | Stryker Endoscopy |
| Brand Name: | Stryker Laparoscopic Instruments |
| Model: | Item Numbers: 0250080178, 0250080174, 0250080180, 0250080315, 0250080179 |
| Affected: | All lots |
| Software version: | |
| Recalling Organisation: | Stryker New Zealand Ltd 515 Mount Wellington Highway Mount Wellington AUCKLAND 1060 |
| Contact Information: | 0800 787 9287 |
| Manufacturer: | Stryker Endoscopy |
| Brand Name: | Stryker Laparoscopic Instruments |
| Model: | Item Number: 0250080235 |
| Affected: | All lots |
| Software version: | |
| Recalling Organisation: | Stryker New Zealand Ltd 515 Mount Wellington Highway Mount Wellington AUCKLAND 1060 |
| Contact Information: | 0800 787 9287 |
| Manufacturer: | Stryker Endoscopy |
| Brand Name: | Stryker Laparoscopic Instruments |
| Model: | Item Number: 0250080158 |
| Affected: | All lots |
| Software version: | |
| Recalling Organisation: | Stryker New Zealand Ltd 515 Mount Wellington Highway Mount Wellington AUCKLAND 1060 |
| Contact Information: | 0800 787 9287 |
| Manufacturer: | Stryker Endoscopy |
| Brand Name: | Stryker Laparoscopic Instruments |
| Model: | Item Number: 0250080156 |
| Affected: | All lots |
| Software version: | |
| Recalling Organisation: | Stryker New Zealand Ltd 515 Mount Wellington Highway Mount Wellington AUCKLAND 1060 |
| Contact Information: | 0800 787 9287 |
| Manufacturer: | Stryker Endoscopy |
| Issue: | The Gravity Unwrapped sterilization cycle and the Ethylene Oxide sterilization cycle have been removed from the Instructions for Use, IFU1000-401-070, as a sterilization option for the Laparoscopic Manual Instruments and Accessories listed above. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 1/12/2014 |
