Database updated: 13 May 2024
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 27599 |
| Brand Name: | NZ FY21-235 |
| Model: | |
| Affected: | Multiple batches |
| Software version: | |
| Recalling Organisation: | Arthrex New Zealand Limited 6 Fox Street Parnell Auckland 1052 |
| Contact Information: | (09) 888 7300 |
| Manufacturer: | Arthrex Inc |
| Brand Name: | NZ FY21-236 |
| Model: | |
| Affected: | Multiple Batches |
| Software version: | |
| Recalling Organisation: | Arthrex New Zealand Limited 6 Fox Street Parnell Auckland 1052 |
| Contact Information: | (09) 888 7300 |
| Manufacturer: | Arthrex Inc |
| Brand Name: | NZ FY21-234 |
| Model: | |
| Affected: | Multiple batches |
| Software version: | |
| Recalling Organisation: | Arthrex New Zealand Limited 6 Fox Street Parnell Auckland 1052 |
| Contact Information: | (09) 888 7300 |
| Manufacturer: | Arthrex Inc |
| Issue: | The manufacturer has recently became aware that devices may not have been sterilized appropriately by a 3rd party organization and is therefore unable to guarantee the sterility of these devices and is removing them from the market. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 16/4/2021 |
