Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 24705 |
| Brand Name: | Biomet Orthopedics - Class I Container |
| Model: | Comprehensive Reverse Shoulder Instrument Case |
| Affected: | |
| Software version: | |
| Recalling Organisation: | Biomet New Zealand Ltd |
| Contact Information: | 0275 522 595 |
| Manufacturer: | Biomet Inc |
| Issue: | The manufacturer is conducting a medical device recall for the Comprehensive Reverse Shoulder Instrument Case Outer and the Comprehensive Reverse Shoulder Instrument Case - Total due to a lack of an adequate sterilization validation. |
| Recall action type: | Recall |
| Recall action: | Product to be returned to supplier |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 25/6/2019 |
