Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 25997 |
| Brand Name: | Biomet Trauma - Instrument Tray I |
| Model: | |
| Affected: | ALL Lots |
| Software version: | |
| Recalling Organisation: | Zimmer Biomet New Zealand Company 210 Khyber Pass Road Grafton Auckland |
| Contact Information: | 09 925 5200 |
| Manufacturer: | Biomet Trauma |
| Brand Name: | CEP Swiss Instruments |
| Model: | |
| Affected: | ALL Lots |
| Software version: | |
| Recalling Organisation: | Zimmer Biomet New Zealand Company 210 Khyber Pass Road Grafton Auckland |
| Contact Information: | 09 925 5200 |
| Manufacturer: | Zimmer GmbH |
| Issue: | The manufacturer is conducting a medical device recall for all lots of the Outer Sheath and the 6.5/8.0MM Screw/Instrument Tray. The affected device and tray that houses the device did not pass steam sterilization process validation testing. The affected device and tray are being obsoleted. Please note that all other instruments in this Tray, excepting the two recalled items have completed the Cleanability and Sterilization Review and these were the only two instruments that failed. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 4/5/2020 |
