Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 13340 |
| Brand Name: | Kerr Cavitec |
| Model: | 00604 |
| Affected: | 0-1335 |
| Software version: | |
| Recalling Organisation: | Henry Schein Regional Ltd 243-249 Bush Road Rosedale North Shore City Auckland 0632 |
| Contact Information: | 0800 808 855 |
| Manufacturer: | Kerr Corporation |
| Issue: | The manufacturer advises that the affected lot of Cavitec may set slower than indicated in the Directions for Use. Although an inconvenience, there are no safety or efficacy issues associated with Cavitec as the product will eventually set. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 8/10/2012 |
